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indoline synthesis</title> <meta name="description" content="Search results for: indole and indoline synthesis"> <meta name="keywords" content="indole and indoline synthesis"> <meta name="viewport" content="width=device-width, initial-scale=1, minimum-scale=1, maximum-scale=1, user-scalable=no"> <meta charset="utf-8"> <link href="https://cdn.waset.org/favicon.ico" type="image/x-icon" rel="shortcut icon"> <link href="https://cdn.waset.org/static/plugins/bootstrap-4.2.1/css/bootstrap.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/plugins/fontawesome/css/all.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/css/site.css?v=150220211555" rel="stylesheet"> </head> <body> <header> <div class="container"> <nav class="navbar navbar-expand-lg navbar-light"> <a class="navbar-brand" href="https://waset.org"> <img src="https://cdn.waset.org/static/images/wasetc.png" alt="Open Science Research Excellence" title="Open Science Research Excellence" /> </a> <button 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action="https://publications.waset.org/abstracts/search"> <div id="custom-search-input"> <div class="input-group"> <i class="fas fa-search"></i> <input type="text" class="search-query" name="q" placeholder="Author, Title, Abstract, Keywords" value="indole and indoline synthesis"> <input type="submit" class="btn_search" value="Search"> </div> </div> </form> </div> </div> <div class="row mt-3"> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Commenced</strong> in January 2007</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Frequency:</strong> Monthly</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Edition:</strong> International</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Paper Count:</strong> 2216</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: indole and indoline synthesis</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2216</span> Design, Synthesis and In-Vitro Antibacterial and Antifungal Activities of Some Novel Spiro[Azetidine-2, 3’-Indole]-2, 4(1’H)-Dione </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ravi%20J.%20Shah">Ravi J. Shah</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The present study deals with the synthesis of novel spiro[azetidine-2, 3’-indole]-2’, 4(1’H)-dione derivative from the reactions of 3-(phenylimino)-1,3-dihydro-2H-indol-2-one derivatives with chloracetyl chloride in presence of triethyl amine (TEA). All the compounds were characterized using IR, 1H NMR, MS and elemental analysis. They were screened for their antibacterial and antifungal activities. Results revealed that, compounds (7a), (7b), (7c), (7d) and (7e) showed very good activity with MIC value of 6.25-12.5 μg/ml against three evaluated bacterial strains and the remaining compounds showed good to moderate activity comparable to standard drugs as antibacterial agents. Compounds (7c) and (7h) displayed equipotent antifungal activity in comparison to standard drugs. Structure-activity relationship study of the compounds showed that the presence of electron withdrawing group substitution at 5’ and 7’ positions of indoline ring and on ortho or para position of phenyl ring increases both antibacterial and antifungal activity of the compound. Henceforth, our findings will have a good impact on chemists and biochemists for further investigations in search of bromine containing spiro fused antimicrobial agents. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=antibacterial%20activity" title="antibacterial activity">antibacterial activity</a>, <a href="https://publications.waset.org/abstracts/search?q=antifungal%20activity" title=" antifungal activity"> antifungal activity</a>, <a href="https://publications.waset.org/abstracts/search?q=2-Azetidinone" title=" 2-Azetidinone"> 2-Azetidinone</a>, <a href="https://publications.waset.org/abstracts/search?q=indoline" title=" indoline "> indoline </a> </p> <a href="https://publications.waset.org/abstracts/26460/design-synthesis-and-in-vitro-antibacterial-and-antifungal-activities-of-some-novel-spiroazetidine-2-3-indole-2-41h-dione" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/26460.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">491</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2215</span> Usy-Cui Zeolite: An Efficient and Reusable Catalyst for Derivatives Indole Synthesis</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hassina%20Harkat">Hassina Harkat</a>, <a href="https://publications.waset.org/abstracts/search?q=Samiha%20Taybe"> Samiha Taybe</a>, <a href="https://publications.waset.org/abstracts/search?q=Salima%20Loucif"> Salima Loucif</a>, <a href="https://publications.waset.org/abstracts/search?q=Val%C3%A9rie%20Beneteau"> Valérie Beneteau</a>, <a href="https://publications.waset.org/abstracts/search?q=Patrick%20Pale"> Patrick Pale </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Indole and its derivatives have attracted great interest because of their importance in the synthetic organic and medicinal chemistry. They are widely used as anti hypertension, anti tubercular, anticancer activity, antiviral, Alzheimer's disease, antioxidant properties, and free radical induced lipid peroxidation. Many drugs and natural products contain indole moiety, such as the vinca alkaloids, fungal metabolites and marine natural products. Generally applicable synthetic methods for indole moiety involve ring closure to form the pyrrole. Indole derivatives can also be accessed by further functionalization of the indole nucleus. Therefore we report a mild and efficient protocol for the synthesis of analogues of indole catalyzed via zeolithe USY doped with CuI under solvent-free conditions. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=indole" title="indole">indole</a>, <a href="https://publications.waset.org/abstracts/search?q=zeolithe" title=" zeolithe"> zeolithe</a>, <a href="https://publications.waset.org/abstracts/search?q=USY-CuI" title=" USY-CuI"> USY-CuI</a>, <a href="https://publications.waset.org/abstracts/search?q=heterogeneous%20catalysis" title=" heterogeneous catalysis"> heterogeneous catalysis</a> </p> <a href="https://publications.waset.org/abstracts/16537/usy-cui-zeolite-an-efficient-and-reusable-catalyst-for-derivatives-indole-synthesis" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/16537.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">585</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2214</span> Development of One-Pot Sequential Cyclizations and Photocatalyzed Decarboxylative Radical Cyclization: Application Towards Aspidospermatan Alkaloids</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Guillaume%20B%C3%A9langer">Guillaume Bélanger</a>, <a href="https://publications.waset.org/abstracts/search?q=Jean-Philippe%20Fontaine"> Jean-Philippe Fontaine</a>, <a href="https://publications.waset.org/abstracts/search?q=Cl%C3%A9mence%20Hauduc"> Clémence Hauduc</a> </p> <p class="card-text"><strong>Abstract:</strong></p> There is an undeniable thirst from organic chemists and from the pharmaceutical industry to access complex alkaloids with short syntheses. While medicinal chemists are interested in the fascinating wide range of biological properties of alkaloids, synthetic chemists are rather interested in finding new routes to access these challenging natural products of often low availability from nature. To synthesize complex polycyclic cores of natural products, reaction cascades or sequences performed one-pot offer a neat advantage over classical methods for their rapid increase in molecular complexity in a single operation. In counterpart, reaction cascades need to be run on substrates bearing all the required functional groups necessary for the key cyclizations. Chemoselectivity is thus a major issue associated with such a strategy, in addition to diastereocontrol and regiocontrol for the overall transformation. In the pursuit of synthetic efficiency, our research group developed an innovative one-pot transformation of linear substrates into bi- and tricyclic adducts applied to the construction of Aspidospermatan-type alkaloids. The latter is a rich class of indole alkaloids bearing a unique bridged azatricyclic core. Despite many efforts toward the synthesis of members of this family, efficient and versatile synthetic routes are still coveted. Indeed, very short, non-racemic approaches are rather scarce: for example, in the cases of aspidospermidine and aspidospermine, syntheses are all fifteen steps and over. We envisaged a unified approach to access several members of the Aspidospermatan alkaloids family. The key sequence features a highly chemoselective formamide activation that triggers a Vilsmeier-Haack cyclization, followed by an azomethine ylide generation and intramolecular cycloaddition. Despite the high density and variety of functional groups on the substrates (electron-rich and electron-poor alkenes, nitrile, amide, ester, enol ether), the sequence generated three new carbon-carbon bonds and three rings in a single operation with good yield and high chemoselectivity. A detailed study of amide, nucleophile, and dipolarophile variations to finally get to the successful combination required for the key transformation will be presented. To complete the indoline fragment of the natural products, we developed an original approach. Indeed, all reported routes to Aspidospermatan alkaloids introduce the indoline or indole early in the synthesis. In our work, the indoline needs to be installed on the azatricyclic core after the key cyclization sequence. As a result, typical Fischer indolization is not suited since this reaction is known to fail on such substrates. We thus envisaged a unique photocatalyzed decarboxylative radical cyclization. The development of this reaction as well as the scope and limitations of the methodology, will also be presented. The original Vilsmeier-Haack and azomethine ylide cyclization sequence as well as the new photocatalyzed decarboxylative radical cyclization will undoubtedly open access to new routes toward polycyclic indole alkaloids and derivatives of pharmaceutical interest in general. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Aspidospermatan%20alkaloids" title="Aspidospermatan alkaloids">Aspidospermatan alkaloids</a>, <a href="https://publications.waset.org/abstracts/search?q=azomethine%20ylide%20cycloaddition" title=" azomethine ylide cycloaddition"> azomethine ylide cycloaddition</a>, <a href="https://publications.waset.org/abstracts/search?q=decarboxylative%20radical%20cyclization" title=" decarboxylative radical cyclization"> decarboxylative radical cyclization</a>, <a href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis" title=" indole and indoline synthesis"> indole and indoline synthesis</a>, <a href="https://publications.waset.org/abstracts/search?q=one-pot%20sequential%20cyclizations" title=" one-pot sequential cyclizations"> one-pot sequential cyclizations</a>, <a href="https://publications.waset.org/abstracts/search?q=photocatalysis" title=" photocatalysis"> photocatalysis</a>, <a href="https://publications.waset.org/abstracts/search?q=Vilsmeier-Haack%20Cyclization" title=" Vilsmeier-Haack Cyclization"> Vilsmeier-Haack Cyclization</a> </p> <a href="https://publications.waset.org/abstracts/139547/development-of-one-pot-sequential-cyclizations-and-photocatalyzed-decarboxylative-radical-cyclization-application-towards-aspidospermatan-alkaloids" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/139547.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">81</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2213</span> Versatile Variation of Fischer Indolization in Green Synthesis of Nitro Substituted Tetrahydrocarbazole</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zubi%20Sadiq">Zubi Sadiq</a>, <a href="https://publications.waset.org/abstracts/search?q=Ghazala%20Yaqub"> Ghazala Yaqub</a>, <a href="https://publications.waset.org/abstracts/search?q=Almas%20Hamid"> Almas Hamid</a> </p> <p class="card-text"><strong>Abstract:</strong></p> We wish to report herein a very stimulating variation in Fischer indole reaction by adopting solvent and catalyst free conditions. A concise synthesis of dinitro tetrahydrocarbazole derivative 3 was introduced without the use of any accelerating agent at ambient temperature with fairly good yield. Product was fully corroborated by UV, FTIR, 1H NMR, 13C NMR, MS, and CHN analysis. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=fischer%20indole%20reaction" title="fischer indole reaction">fischer indole reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=neutral%20medium" title=" neutral medium"> neutral medium</a>, <a href="https://publications.waset.org/abstracts/search?q=solvent%20free%20synthesis" title=" solvent free synthesis"> solvent free synthesis</a>, <a href="https://publications.waset.org/abstracts/search?q=tetrahydrocarbazole" title=" tetrahydrocarbazole"> tetrahydrocarbazole</a> </p> <a href="https://publications.waset.org/abstracts/11748/versatile-variation-of-fischer-indolization-in-green-synthesis-of-nitro-substituted-tetrahydrocarbazole" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/11748.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">359</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2212</span> Green, Smooth and Easy Electrochemical Synthesis of N-Protected Indole Derivatives</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sarah%20Fahad%20Alajmi">Sarah Fahad Alajmi</a>, <a href="https://publications.waset.org/abstracts/search?q=Tamer%20Ezzat%20Youssef"> Tamer Ezzat Youssef</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Here, we report a simple method for the direct conversion of 6-Nitro-1H-indole into <em>N</em>-substituted indoles via electrochemical dehydrogenative reaction with halogenated reagents under strongly basic conditions through N–R bond formation. The <em>N</em>-protected indoles have been prepared under moderate and scalable electrolytic conditions. The conduct of the reactions was performed in a simple divided cell under constant current without oxidizing reagents or transition-metal catalysts. The synthesized products have been characterized via UV/Vis spectrophotometry, 1H-NMR, and FTIR spectroscopy. A possible reaction mechanism is discussed based on the <em>N</em>-protective products. This methodology could be applied to the synthesis of various biologically active <em>N</em>-substituted indole derivatives. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=green%20chemistry" title="green chemistry">green chemistry</a>, <a href="https://publications.waset.org/abstracts/search?q=1H-indole" title=" 1H-indole"> 1H-indole</a>, <a href="https://publications.waset.org/abstracts/search?q=heteroaromatic" title=" heteroaromatic"> heteroaromatic</a>, <a href="https://publications.waset.org/abstracts/search?q=organic%20electrosynthesis" title=" organic electrosynthesis"> organic electrosynthesis</a> </p> <a href="https://publications.waset.org/abstracts/129536/green-smooth-and-easy-electrochemical-synthesis-of-n-protected-indole-derivatives" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/129536.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">161</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2211</span> Attempts for the Synthesis of Indol-Ring Fluorinated Tryptophan Derivatives to Enhance the Activity of Antimicrobial Peptides</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Anita%20K.%20Kovacs">Anita K. Kovacs</a>, <a href="https://publications.waset.org/abstracts/search?q=Peter%20Hegyes"> Peter Hegyes</a>, <a href="https://publications.waset.org/abstracts/search?q=Zsolt%20Bozso"> Zsolt Bozso</a>, <a href="https://publications.waset.org/abstracts/search?q=Gabor%20Toth"> Gabor Toth</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Fluorination has been used extensively by the pharmaceutical industry as a strategy to improve the pharmacokinetics of drugs due to its effectiveness in increasing the potency of antimicrobial peptides (AMPs). Multiple-fluorinated indole-ring-containing tryptophan derivatives have the potential of having better antimicrobial activity than the widely used mono-fluorinated indole-ring containing tryptophan derivatives, but they are not available commercially. Therefore, our goal is to synthesize multiple-fluorinated indole-ring containing tryptophan derivatives to incorporate them into AMPs to enhance their antimicrobial activity. During our work, we are trying several methods (classical organic synthesis, enzymic synthesis, and solid phase peptide synthesis) for the synthesis of the said compounds, with mixed results. With classical organic synthesis (four different routes), we did not get the desired results. The reaction of serin with substituted indole in the presence of acetic anhydride led to racemic tryptophane; with the reaction of protected serin with indole in the presence of nickel complex was unsuccessful; the reaction of serin containing protected dipeptide with disuccinimidyl carbonate we achieved a tryptophane containing dipeptide, its chiral purity is being examined; the reaction of alcohol with substituted indole in the presence of copper complex was successful, but it was only a test reaction, we could not reproduce the same result with serine. The undergoing tryptophan-synthase method has shown some potential, but our work has not been finished yet. The successful synthesis of the desired multiple-fluorinated indole-ring-containing tryptophan will be followed by solid phase peptide synthesis in order to incorporate it into AMPs to enhance their antimicrobial activity. The successful completion of these phases will mean the possibility of manufacturing new, effective AMPs. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=halogenation" title="halogenation">halogenation</a>, <a href="https://publications.waset.org/abstracts/search?q=fluorination" title=" fluorination"> fluorination</a>, <a href="https://publications.waset.org/abstracts/search?q=tryptophan" title=" tryptophan"> tryptophan</a>, <a href="https://publications.waset.org/abstracts/search?q=enhancement%20of%20antimicrobial%20activity" title=" enhancement of antimicrobial activity"> enhancement of antimicrobial activity</a> </p> <a href="https://publications.waset.org/abstracts/152468/attempts-for-the-synthesis-of-indol-ring-fluorinated-tryptophan-derivatives-to-enhance-the-activity-of-antimicrobial-peptides" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/152468.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">97</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2210</span> Ag (I) Catalyzed Domino Carbonyl and Alkyne Activation: A Smooth Entry to 2, 2′-Di-Substituted 3, 3′-Bisindolylarylmethanes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Swastik%20Karmakar">Swastik Karmakar</a>, <a href="https://publications.waset.org/abstracts/search?q=Prasanta%20Das"> Prasanta Das</a>, <a href="https://publications.waset.org/abstracts/search?q=Shital%20K.%20Chattopadhyay"> Shital K. Chattopadhyay</a> </p> <p class="card-text"><strong>Abstract:</strong></p> An eﬃcient synthesis of symmetrical 2, 2′-Di-substituted 3, 3′-bisindolylarylmethanes (BIAMs) having different aryl and hetero-aryl moieties has been developed by Ag(I)-catalyzed indolyzation and a sequential deoxygenative addition involving o-alkynylanilines and aryl/hetero-aryl aldehydes as substrates. Alkyne and carbonyl units could be activated by Ag (I) simultaneously which results in a domino 5-endo-dig indole annulation, addition of C3 of this indole nucleus to the carbonyl carbon in addition to second indole annulation, and its dehydroxylative addition to the same carbonyl carbon to furnish BIAMs in excellent yield. As 3, 3′-bisindolylmethanes (BIMs) are biologically significant scaﬀolds, this moiety with further substitutions at the indole core could ﬁnd some important use in medicinal chemistry. The methodology developed is atom-economic and involves more accessible silver salts, which could be useful for large-scale synthesis. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=alkyne" title="alkyne">alkyne</a>, <a href="https://publications.waset.org/abstracts/search?q=3" title=" 3"> 3</a>, <a href="https://publications.waset.org/abstracts/search?q=3%E2%80%B2-Bisindolylarylmethanes" title=" 3′-Bisindolylarylmethanes"> 3′-Bisindolylarylmethanes</a>, <a href="https://publications.waset.org/abstracts/search?q=carbonyl" title=" carbonyl"> carbonyl</a>, <a href="https://publications.waset.org/abstracts/search?q=domino" title=" domino"> domino</a>, <a href="https://publications.waset.org/abstracts/search?q=5-endo-dig%20indole%20annulation" title=" 5-endo-dig indole annulation"> 5-endo-dig indole annulation</a>, <a href="https://publications.waset.org/abstracts/search?q=silver%20catalyst" title=" silver catalyst"> silver catalyst</a> </p> <a href="https://publications.waset.org/abstracts/63170/ag-i-catalyzed-domino-carbonyl-and-alkyne-activation-a-smooth-entry-to-2-2-di-substituted-3-3-bisindolylarylmethanes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/63170.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">209</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2209</span> Synthesis and Evaluation of Antioxidant Behavior of Some Indole-Based Melatonin Derivatives</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Eddy%20Neuhaus">Eddy Neuhaus</a>, <a href="https://publications.waset.org/abstracts/search?q=Hanif%20Shirinzadeh"> Hanif Shirinzadeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Cigdem%20Karaaslan"> Cigdem Karaaslan</a>, <a href="https://publications.waset.org/abstracts/search?q=Elif%20Ince"> Elif Ince</a>, <a href="https://publications.waset.org/abstracts/search?q=Hande%20Gurer-Orhan"> Hande Gurer-Orhan</a>, <a href="https://publications.waset.org/abstracts/search?q=Sibel%20Suzen"> Sibel Suzen</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Reactive oxygen species (ROS) and oxidative stress can cause fatal damage to essential cell structures, including DNA. It is known that use of antioxidants could be advantageous in the prevention of various diseases such as cancer, cardiovascular diseases and neurodegenerative disorders. Since antioxidant properties of the indole ring-containing melatonin (MLT) has been described and evaluated, MLT-related compounds such as MLT metabolites and synthetic analogues are under investigation to determine which exhibit the highest activity with the lowest side-effects. Owing to indole and hydrazones appealing physiological properties and are mostly found in numerous biologically active compounds a series of indole-7-carbaldehyde hydrazone derivatives were synthesized, characterized and in vitro antioxidant activity was investigated by evaluating their reducing effect against oxidation of a redox-sensitive fluorescent probe. Cytotoxicity potential of all indole-based MLT analogues was investigated both by lactate dehydrogenase leakage assay and by MTT assay. This work was supported by The Scientific and Technological Research Council of Turkey (TÜBİTAK) Research and Development Grant 112S599. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=melatonin" title="melatonin">melatonin</a>, <a href="https://publications.waset.org/abstracts/search?q=antioxidant%20activity" title=" antioxidant activity"> antioxidant activity</a>, <a href="https://publications.waset.org/abstracts/search?q=indole" title=" indole"> indole</a>, <a href="https://publications.waset.org/abstracts/search?q=hydrazone" title=" hydrazone"> hydrazone</a>, <a href="https://publications.waset.org/abstracts/search?q=oxidative%20stress" title=" oxidative stress"> oxidative stress</a> </p> <a href="https://publications.waset.org/abstracts/19943/synthesis-and-evaluation-of-antioxidant-behavior-of-some-indole-based-melatonin-derivatives" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/19943.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">484</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2208</span> Synthesis and Pharmacological Activity of Some Oxyindole Derivatives</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Vivek%20Singh%20Bhadauria">Vivek Singh Bhadauria</a>, <a href="https://publications.waset.org/abstracts/search?q=Abhishek%20Pandey"> Abhishek Pandey</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Indole-2,3-diones are known for their various biological activities. By suitable control of a substituent, different novel indole-2,3-diones were synthesized. In this present study, various Schiff and Mannich bases were synthesized and characterized, and evaluated their for different pharmacological activities. The compounds were prepared by reacting indole-2,3-dione with benzyl chloride and 4-substituted thiosemicarbazides. All the synthesized compounds were characterized by the TLC, MP, Elemental analysis, FTIR, 1H-NMR and Mass spectroscopy. The compounds have been evaluated for their anticancer, antituberculosis, anticonvulsant, antiinflammatory as well as anti-SARS activity and the results are presented. Some of compounds possessed different pharmacological activity at a concentration of 200 mg/kg body weight and even at lower concentration. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=indoles" title="indoles">indoles</a>, <a href="https://publications.waset.org/abstracts/search?q=isatin" title=" isatin"> isatin</a>, <a href="https://publications.waset.org/abstracts/search?q=NMR" title=" NMR"> NMR</a>, <a href="https://publications.waset.org/abstracts/search?q=biological%20activities" title=" biological activities"> biological activities</a> </p> <a href="https://publications.waset.org/abstracts/2954/synthesis-and-pharmacological-activity-of-some-oxyindole-derivatives" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/2954.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">355</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2207</span> Characterization of Monoclonal Antibodies Specific for Synthetic Cannabinoids</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hiroshi%20Nakayama">Hiroshi Nakayama</a>, <a href="https://publications.waset.org/abstracts/search?q=Yuji%20Ito"> Yuji Ito</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Synthetic cannabinoids have attracted much public attention recently in Japan. 1-pentyl-3-(1-naphthoyl)-indole (JWH-018), 1-pentyl-2-methyl-3-(1-naphthoyl) indole (JWH-015), 1-(5-fluoropentyl)-3- (1-(2,2,3,3- tetramethylcyclopropyl)) indole (XLR-11) and 1-methyl-3- (1-admantyl) indole (JWH-018 adamantyl analog) are known as synthetic cannabinoids and are also considered dangerous illegal drugs in Japan. It has become necessary to develop sensitive and useful methods for detection of synthetic cannabinoids. We produced two monoclonal antibodies (MAb) against synthetic cannabinoids, named NT1 (IgG1) and NT2 (IgG1), using Hybridoma technology. The cross-reactivity of these produced MAbs was evaluated using a competitive enzyme-linked immunosorbent assay (ELISA). In the results, we found both of these antibodies recognize many kinds of synthetic cannabinoids analog. However, neither of these antibodies recognizes naphtoic acid, 1-methyl-indole and indole known as a raw material of synthetic cannabinoid. Thus, the MAbs produced in this study could be a useful tool for the detection of synthetic cannabinoids. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=ELISA" title="ELISA">ELISA</a>, <a href="https://publications.waset.org/abstracts/search?q=monoclonal%20antibody" title=" monoclonal antibody"> monoclonal antibody</a>, <a href="https://publications.waset.org/abstracts/search?q=sensor" title=" sensor"> sensor</a>, <a href="https://publications.waset.org/abstracts/search?q=synthetic%20cannabinoid" title=" synthetic cannabinoid"> synthetic cannabinoid</a> </p> <a href="https://publications.waset.org/abstracts/51072/characterization-of-monoclonal-antibodies-specific-for-synthetic-cannabinoids" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/51072.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">355</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2206</span> Silica Sulfuric Acid as an Efficient Catalyst One-Pot Three-Component Aza-Friedel-Crafts Reactions of 2-(thiophen-2-yl)-1H-Indole, Aldehydes, and N-Substituted Anilines</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nagwa%20Mourad%20Abdelazeem">Nagwa Mourad Abdelazeem</a>, <a href="https://publications.waset.org/abstracts/search?q=Marwa%20El-hussieny"> Marwa El-hussieny</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Multicomponent reactions (MCRs), one-pot reactions form products from more than two different starting compounds. (MCRs) are ideal reaction systems leading to high structural diversity and molecular complexity through a single transformation. (MCRs) have a lot of advantage such as higher yield, less waste generation, use of readily available starting materials and high atom. (MCRs) provide a rapid process for efficient synthesis of key structures in discovery of drug on the other hand silica sulfuric acid (SSA) has been used as an efficient heterogeneous catalyst for many organic transformations. (SSA) is low cost, ease of preparation, catalyst recycling, and ease of handling, so in this article we used 2-(thiophen-2-yl)-1H-indole, N-substituted anilines and aldehyde in the presence of silica sulfuric acid (SSA) as a catalyst in water as solvent at room temperature to prepare 3,3'-(phenylmethylene)bis(2-(thiophen-2-yl)-1H-indole) and N-methyl-4-(phenyl(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)aniline derivatives Via one-pot reaction. Compound 2-(thiophen-2-yl)-1H-indole belongs to the ubiquitous class of indoles which enjoy broad synthetic, biological and industrial applications ]. Cancer is considered the first or second most common reason of death all through the world. So the synthesized compounds will be tested as anticancer. We expected the synthesized compounds will give good results comparison to the reference drug. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=aldehydes" title="aldehydes">aldehydes</a>, <a href="https://publications.waset.org/abstracts/search?q=aza-friedel-crafts%20reaction" title=" aza-friedel-crafts reaction"> aza-friedel-crafts reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=indole" title=" indole"> indole</a>, <a href="https://publications.waset.org/abstracts/search?q=multicomponent%20reaction" title=" multicomponent reaction"> multicomponent reaction</a> </p> <a href="https://publications.waset.org/abstracts/158238/silica-sulfuric-acid-as-an-efficient-catalyst-one-pot-three-component-aza-friedel-crafts-reactions-of-2-thiophen-2-yl-1h-indole-aldehydes-and-n-substituted-anilines" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/158238.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">97</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2205</span> Synthesis of Biologically Active Heterocyclic Compounds via C-H Bond Activation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Neeraj%20Kumar%20Mishra">Neeraj Kumar Mishra</a>, <a href="https://publications.waset.org/abstracts/search?q=In%20Su%20Kim"> In Su Kim</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The isoindoline, indazole and indole heterocycles are ubiquitous structural motif found in heterocyclic compounds as they exhibit biological and medicinal applications. For example, isoindoline motif is present in molecules that act as endothelin-A receptor antagonists and dipeptidyl peptidase inhibitors. Moreover, isoindoline derivatives are very crucial constituents in the field of materials science as attractive candidates for organic light-emitting devices. However, compounds containing the indazole motif are known to exhibit to a variety of biological activities, such as estrogen receptor, HIV protease inhibition and anti-tumor activity. The prevalence of indazoles and indoles has led to the development of many useful methods for their preparation. Thus, isoindoline, indazole and indole heterocycles can be new candidates for the next generation of pharmaceuticals. Therefore, the development of highly eﬃcient strategies for the formation of these heterocyclic architectures is an area of great interest in organic synthesis. The past years, transition-metal-catalyzed C−H activation followed by annulation reaction has been frequently used as a powerful tool to construct various heterocycles. Herein, we describe our recent achievements about the transition-metal-catalyzed tandem cyclization reactions of N-benzyltriflamides, 1,2-disubstituted arylhydrazines, acetanilides, etc. via C−H bond activation to access the corresponding bioactive heterocylic scaffolds. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biologically%20active" title="biologically active">biologically active</a>, <a href="https://publications.waset.org/abstracts/search?q=C-H%20activation" title=" C-H activation"> C-H activation</a>, <a href="https://publications.waset.org/abstracts/search?q=heterocyclic%20compounds" title=" heterocyclic compounds"> heterocyclic compounds</a>, <a href="https://publications.waset.org/abstracts/search?q=transition-metal%20catalysts" title=" transition-metal catalysts"> transition-metal catalysts</a> </p> <a href="https://publications.waset.org/abstracts/58546/synthesis-of-biologically-active-heterocyclic-compounds-via-c-h-bond-activation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/58546.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">309</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2204</span> Direct Palladium-Catalyzed Selective N-Allylation of 2,3-Disubstituted Indoles with Allylic Alcohols in Water</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Bai-Jing%20Peng">Bai-Jing Peng</a>, <a href="https://publications.waset.org/abstracts/search?q=Shyh-Chyun%20Yang"> Shyh-Chyun Yang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Organic reactions in water have recently attracted much attention, not only because unique reactivity is often observed in water but also because water is a safe and economical substitute for conventional organic solvents. Thus, development of environmental safe, atom-economical reactions in water is one of the most important goals of synthetic chemistry. The recent paper has documented renewed interest in the use of allylic substrates in the synthesis of new C−C, C−N, and C−O bonds. We have reported our attempts and some successful applications of a process involving the C-O bond cleavage catalyzed by palladium or platinum complexes in water. Because of the importance of heterocycle indole derivatives, much effort has been directed toward the development of methods for functionalization of the indole nucleus at N1 site. In our research, the palladium-catalyzed 2,3-disubstitued indoles with allylic alcohols was investigated under different conditions. Herein, we will establish a simple, convenient, and efficient method, which affords high yields of allylated indoles. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=palladium-catalyzed" title="palladium-catalyzed">palladium-catalyzed</a>, <a href="https://publications.waset.org/abstracts/search?q=allylic%20alcohols" title=" allylic alcohols"> allylic alcohols</a>, <a href="https://publications.waset.org/abstracts/search?q=indoles" title=" indoles"> indoles</a>, <a href="https://publications.waset.org/abstracts/search?q=water" title=" water"> water</a>, <a href="https://publications.waset.org/abstracts/search?q=allylation" title=" allylation"> allylation</a> </p> <a href="https://publications.waset.org/abstracts/71957/direct-palladium-catalyzed-selective-n-allylation-of-23-disubstituted-indoles-with-allylic-alcohols-in-water" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/71957.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">238</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2203</span> Cholinesterase Inhibitory Indole Alkaloids from the Bark of Rauvolfia reflexa</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mehran%20Fadaeinasab">Mehran Fadaeinasab</a>, <a href="https://publications.waset.org/abstracts/search?q=Alireza%20Basiri"> Alireza Basiri</a>, <a href="https://publications.waset.org/abstracts/search?q=Yalda%20Kia"> Yalda Kia</a>, <a href="https://publications.waset.org/abstracts/search?q=Hamed%20Karimian"> Hamed Karimian</a>, <a href="https://publications.waset.org/abstracts/search?q=Hapipah%20Mohd%20Ali"> Hapipah Mohd Ali</a>, <a href="https://publications.waset.org/abstracts/search?q=Vikneswaran%20Murugaiyah"> Vikneswaran Murugaiyah</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Two new, rauvolfine C and 3- methyl-10,11-dimethoxyl-6- methoxycarbonyl- β- carboline, along with five known indole alkaloids, macusine B, vinorine, undulifoline, isoresrpiline and rescinnamine were isolated from the bark of Rauvolfia reflexa. All the compounds showed good to moderate cholinesterase inhibitory activity with IC50 values in the range of 8.06 to 73.23 πM, except rauvolfine C that was inactive against acetylcholinesterase (AChE). Rescinnamine, a dual inhibitor was found to be the most potent inhibitor among the isolated alkaloids against both AChE and butyrylcholinesterase (BChE). Molecular docking revealed that rescinnamine interacted differently on AChE and BChE, by means of hydrophobic interactions and hydrogen bonding. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Rauvolfia%20reflexa" title="Rauvolfia reflexa">Rauvolfia reflexa</a>, <a href="https://publications.waset.org/abstracts/search?q=indole%20alkaloids" title=" indole alkaloids"> indole alkaloids</a>, <a href="https://publications.waset.org/abstracts/search?q=acetylcholinesterase" title=" acetylcholinesterase"> acetylcholinesterase</a>, <a href="https://publications.waset.org/abstracts/search?q=butyrylcholinesterase" title=" butyrylcholinesterase"> butyrylcholinesterase</a>, <a href="https://publications.waset.org/abstracts/search?q=molecular%20docking" title=" molecular docking"> molecular docking</a> </p> <a href="https://publications.waset.org/abstracts/30034/cholinesterase-inhibitory-indole-alkaloids-from-the-bark-of-rauvolfia-reflexa" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/30034.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">592</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2202</span> Somatic Embryogenesis Derived from Protoplast of Murraya Paniculata L. Jack and Their Regeneration into Plant Flowering in vitro</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hasan%20Basri%20Jumin">Hasan Basri Jumin</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The in vitro flowering of orange jessamine plantlets derived from protoplast was affected by the manipulation of plant growth regulators, sugar and light conditions. MT basal medium containing 5% sucrose and supplemented with 0.001 mg 1-1 indole-acetic-acid was found to be a suitable medium for development of globular somatic embryos derived from protoplasts to form heart-shaped somatic embryos with cotyledon-like structures. The highest percentage (85 %) of flowering was achieved with plantlet on half-strength MT basal medium containing 5% sucrose and 0.001 mg1-1 indole-acetic-acid in light. Exposure to darkness for more than 3 weeks followed by re-exposure to light reduced flowering. Flowering required a 10-day exposure to indole-acetic-acid. Photoperiod with 18 h and 79.4 µmol m-2 s-1 light intensity promoted in vitro flowering in high frequencies. The sucrose treatment affected the flower bud size distribution. Flower buds originating from plantlet derived from protoplasts developed into normal flowers. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=indole-acetc-acid" title="indole-acetc-acid">indole-acetc-acid</a>, <a href="https://publications.waset.org/abstracts/search?q=light-intensity" title=" light-intensity"> light-intensity</a>, <a href="https://publications.waset.org/abstracts/search?q=Murraya-paniculata" title=" Murraya-paniculata"> Murraya-paniculata</a>, <a href="https://publications.waset.org/abstracts/search?q=photoperiod" title=" photoperiod"> photoperiod</a>, <a href="https://publications.waset.org/abstracts/search?q=plantlet" title=" plantlet"> plantlet</a>, <a href="https://publications.waset.org/abstracts/search?q=Zeatin" title=" Zeatin"> Zeatin</a> </p> <a href="https://publications.waset.org/abstracts/28393/somatic-embryogenesis-derived-from-protoplast-of-murraya-paniculata-l-jack-and-their-regeneration-into-plant-flowering-in-vitro" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/28393.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">418</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2201</span> Regioselective Nucleophilic Substitution of the Baylis-Hillman Adducts with Iodine</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zahid%20Shafiq">Zahid Shafiq</a>, <a href="https://publications.waset.org/abstracts/search?q=Li%20Liu"> Li Liu</a>, <a href="https://publications.waset.org/abstracts/search?q=Dong%20Wang"> Dong Wang</a>, <a href="https://publications.waset.org/abstracts/search?q=Yong-Jun%20Chen"> Yong-Jun Chen</a> </p> <p class="card-text"><strong>Abstract:</strong></p> As synthetic organic methods are increasingly concerned with the growing importance of sustainable chemistry, iodine recently has emerged as an inexpensive, non-toxic, readily available and environmentally benign catalyst for various organic transformations to afford the corresponding products in high yields with high regio- and chemoselectivity. Iodine has found widespread applications in various organic synthesis such as Michael addition, coupling reaction and also in the multicomponent synthesis where it can efficiently activate C=C, C=O, C=N, and so forth. Iodine not only has been shown to be an efficient mild Lewis acid in various processes, but also due to its moderate nature, and water tolerance, reactions catalyzed by iodine can be effectively carried out in neutral media under very mild conditions. We have successfully described an efficient procedure for the nucleophilic substitution of the Baylis-Hillman (BH) adducts and their corresponding acetates with indoles to get α-substitution product using catalytic Silver Triflate (AgOTf) as Lewis acid. At this point, we were interested to develop an environmentally benign catalytic system to effect this substitution reaction and to avoid the use of metal Lewis acid as a catalyst. Since, we observed the formation of -product during the course of the reaction, we also became interested to explore the reaction conditions in order to control regioselectivity and to obtain both regioisomers. The developed methodology resulted in regioselective substitution products with controlled selectivity. Further, the substitution products were used to synthesize various Tri- and Tetracyclo Azepino indole derivatives via reductive amination. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=indole" title="indole">indole</a>, <a href="https://publications.waset.org/abstracts/search?q=regioselective" title=" regioselective"> regioselective</a>, <a href="https://publications.waset.org/abstracts/search?q=Baylis-Hillman" title=" Baylis-Hillman"> Baylis-Hillman</a>, <a href="https://publications.waset.org/abstracts/search?q=substitution" title=" substitution"> substitution</a> </p> <a href="https://publications.waset.org/abstracts/110900/regioselective-nucleophilic-substitution-of-the-baylis-hillman-adducts-with-iodine" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/110900.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">198</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2200</span> Effects of Indole on Aerobic Biodegradation of Butanoic Acid by Pseudomonas aeruginosa and Serratia marcescens</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=J.%20B.%20J.%20Njalam%E2%80%99mano">J. B. J. Njalam’mano</a>, <a href="https://publications.waset.org/abstracts/search?q=E.%20M.%20N.%20Chirwa"> E. M. N. Chirwa</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In low resource settings in Africa and other developing regions, pit latrines remain the dominant basic minimum acceptable form of sanitation. However, unpleasant smells-malodours emitted from faecal sludge in the pit latrines, which elicit disgusting or repulsive response, are one of the factors that thwart people to use latrines and instead opt for open defecation as an alternative. This provides an important but often overlooked major impediment, dissuading people from adopting and using the pit latrines hence affecting successful, effective sanitation promotion. The malodours are primarily attributed to four odorants: butanoic acid (C₄H₈O₂), dimethyl trisulphide (C₂H₆S₃), indole (C₈H₇N) and para-cresol (C₇H₈O). Several pit latrine deodorisation methods such as addition of carbonous materials, use of ventilation systems and urine separation are available, and they continue to occupy their niche, but social, economic, environmental and technological shortfalls remain. Bioremediation has been gaining popularity because it is inexpensive, simple to operate and environmentally friendly. Recently, the biodegradation of butanoic acid as individual odorant has been studied. However, to the best of our knowledge, there have been no kinetic studies of the butanoic acid in the presence of other key odorous compounds. In this study, a series of experiments were conducted to investigate the effects of indole on the removal of butanoic acid under aerobic conditions using indigenous bacteria strains, Pseudomonas aeruginosa, and Serratia marcescens isolated from faecal sludge as pure cultures as well as mixed cultures. In this purpose, butanoic acid removal was performed in a batch reactor containing the bacterial strains in mineral salt medium (MSM) amended with 3000 ppm of butanoic acid at the temperature of 30°C, under continuous stirring rate of 150 rpm and the concentration of indole was varied from 50-200 ppm. The initial pH of the solution was in the range of 6.0-7.2. Overall, there were significant differences in the bacterial growth rate and total butanoic acid removal dependent on the concentration of indole in the solution. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biodegradation" title="biodegradation">biodegradation</a>, <a href="https://publications.waset.org/abstracts/search?q=butanoic%20acid" title=" butanoic acid"> butanoic acid</a>, <a href="https://publications.waset.org/abstracts/search?q=indole" title=" indole"> indole</a>, <a href="https://publications.waset.org/abstracts/search?q=pit%20latrine" title=" pit latrine"> pit latrine</a> </p> <a href="https://publications.waset.org/abstracts/73333/effects-of-indole-on-aerobic-biodegradation-of-butanoic-acid-by-pseudomonas-aeruginosa-and-serratia-marcescens" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/73333.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">195</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2199</span> Preparation and Antioxidant Activity of Heterocyclic Indole Derivatives</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Tunca%20Gul%20Altuntas">Tunca Gul Altuntas</a>, <a href="https://publications.waset.org/abstracts/search?q=Aziz%20Baydar"> Aziz Baydar</a>, <a href="https://publications.waset.org/abstracts/search?q=Cemre%20Acar"> Cemre Acar</a>, <a href="https://publications.waset.org/abstracts/search?q=Sezen%20Y%C4%B1lmaz"> Sezen Yılmaz</a>, <a href="https://publications.waset.org/abstracts/search?q=Tulay%20Coban"> Tulay Coban</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Free radicals, which are generated in many bioorganic redox processes, play a role in the pathogenesis of several diseases including cancer, arthritis, hemorrhagic shock, inflammatory, cardiovascular, neurodegenerative diseases and age-related degenerative brain diseases. Exposures of normal cell to free radical damages several structures, oxidizes nucleic acids, proteins, lipids, or DNA. Compounds interfere with the action of reactive oxygen species might be useful in prevention and treatment of these pathologies. A series of indole compounds containing piperazine ring were synthesized. Coupling of indole-2-carboxylic acid with monosubstituted piperazines was accomplished with 1,1’-carbonyldiimidazole (CDI) in a good yield. The structures of prepared compounds were verified in good agreement with their 1H NMR (nuclear magnetic resonance), MS (mass spectrophotometry), and IR (infrared spectrophotometry) characteristics. In this work, all synthetized indole derivatives were screened in vitro for their antioxidative potential against vitamin E (α-tocopherol) using different antioxidant assays such as superoxide anion formation, lipid peroxidation levels in rat liver, and 2,2-diphenyl-1-picrylhydrazyl (DPPH) stable radical scavenging activity. The synthesized compounds showed various levels of inhibition compared to vitamin E. This may give promising results for the development of new antioxidant agents. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=antioxidant" title="antioxidant">antioxidant</a>, <a href="https://publications.waset.org/abstracts/search?q=indoles" title=" indoles"> indoles</a>, <a href="https://publications.waset.org/abstracts/search?q=piperazines" title=" piperazines"> piperazines</a>, <a href="https://publications.waset.org/abstracts/search?q=reactive%20oxygen%20species" title=" reactive oxygen species"> reactive oxygen species</a> </p> <a href="https://publications.waset.org/abstracts/91784/preparation-and-antioxidant-activity-of-heterocyclic-indole-derivatives" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/91784.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">231</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2198</span> Biosynthesis of Natural and Halogenated Plant Alkaloids in Yeast</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Beata%20J.%20Lehka">Beata J. Lehka</a>, <a href="https://publications.waset.org/abstracts/search?q=Samuel%20A.%20Bradley"> Samuel A. Bradley</a>, <a href="https://publications.waset.org/abstracts/search?q=Frederik%20G.%20Hansson"> Frederik G. Hansson</a>, <a href="https://publications.waset.org/abstracts/search?q=Khem%20B.%20Adhikari"> Khem B. Adhikari</a>, <a href="https://publications.waset.org/abstracts/search?q=Daniela%20Rago"> Daniela Rago</a>, <a href="https://publications.waset.org/abstracts/search?q=Paulina%20Rubaszka"> Paulina Rubaszka</a>, <a href="https://publications.waset.org/abstracts/search?q=Ahmad%20K.%20Haidar"> Ahmad K. Haidar</a>, <a href="https://publications.waset.org/abstracts/search?q=Ling%20Chen"> Ling Chen</a>, <a href="https://publications.waset.org/abstracts/search?q=Lea%20G.%20Hansen"> Lea G. Hansen</a>, <a href="https://publications.waset.org/abstracts/search?q=Olga%20Gudich"> Olga Gudich</a>, <a href="https://publications.waset.org/abstracts/search?q=Konstantina%20Giannakou"> Konstantina Giannakou</a>, <a href="https://publications.waset.org/abstracts/search?q=Yoko%20Nakamura"> Yoko Nakamura</a>, <a href="https://publications.waset.org/abstracts/search?q=Thomas%20Dug%C3%A9%20de%20Bernonville"> Thomas Dugé de Bernonville</a>, <a href="https://publications.waset.org/abstracts/search?q=Konstantinos%20Koudounas"> Konstantinos Koudounas</a>, <a href="https://publications.waset.org/abstracts/search?q=Sarah%20E.%20O%E2%80%99Connor"> Sarah E. O’Connor</a>, <a href="https://publications.waset.org/abstracts/search?q=Vincent%20Courdavault"> Vincent Courdavault</a>, <a href="https://publications.waset.org/abstracts/search?q=Jay%20D.%20Keasling"> Jay D. Keasling</a>, <a href="https://publications.waset.org/abstracts/search?q=Jie%20Zhang"> Jie Zhang</a>, <a href="https://publications.waset.org/abstracts/search?q=Michael%20K.%20Jensen"> Michael K. Jensen</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Monoterpenoid indole alkaloids (MIAs) represent a large class of natural plant products with marketed pharmaceutical activities against a wide range of applications, including cancer and mental disorders. Halogenated MIAs have shown improved pharmaceutical properties; however, characterisation and synthesis of new-to-nature halogenated MIAs remain a challenge in slow-growing plants with limited genetic tractability. Here, we demonstrate a platform for de novo biosynthesis of two bioactive MIAs, serpentine and alstonine, in baker’s yeast Saccharomyces cerevisiae, reaching titers of 8.85 mg/L and 4.48 mg/L, respectively, when cultivated in fed-batch micro bioreactors. Using this MIA biosynthesis platform, we undertake a systematic exploration of the derivative space surrounding these compounds and produce halogenated MIAs. The aim of the current study is to develop a fermentation process for halogenated MIAs. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=monoterpenoid%20indole%20alkaloids" title="monoterpenoid indole alkaloids">monoterpenoid indole alkaloids</a>, <a href="https://publications.waset.org/abstracts/search?q=Saccharomyces%20cerevisiae" title=" Saccharomyces cerevisiae"> Saccharomyces cerevisiae</a>, <a href="https://publications.waset.org/abstracts/search?q=halogenated%20derivatives" title=" halogenated derivatives"> halogenated derivatives</a>, <a href="https://publications.waset.org/abstracts/search?q=fermentation" title=" fermentation"> fermentation</a> </p> <a href="https://publications.waset.org/abstracts/150245/biosynthesis-of-natural-and-halogenated-plant-alkaloids-in-yeast" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/150245.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">210</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2197</span> Synthesis and Application of an Organic Dye in Nanostructure Solar Cells Device</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20Hoseinnezhad">M. Hoseinnezhad</a>, <a href="https://publications.waset.org/abstracts/search?q=K.%20Gharanjig"> K. Gharanjig</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Two organic dyes comprising carbazole as the electron donors and cyanoacetic acid moieties as the electron acceptors were synthesized. The organic dye was prepared by standard reaction from carbazole as the starting material. To this end, carbazole was reacted with bromobenzene and further oxidation and reacted with cyanoacetic acid. The obtained organic dye was purified and characterized using differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance (<sup>1</sup>HNMR), carbon nuclear magnetic resonance (<sup>13</sup>CNMR) and elemental analysis. The influence of heteroatom on carbazole donors and cyno substitution on the acid acceptor is evidenced by spectral and electrochemical photovoltaic experiments. Finally, light fastness properties for organic dye were investigated. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=dye-sensitized%20solar%20cells" title="dye-sensitized solar cells">dye-sensitized solar cells</a>, <a href="https://publications.waset.org/abstracts/search?q=indoline%20dye" title=" indoline dye"> indoline dye</a>, <a href="https://publications.waset.org/abstracts/search?q=nanostructure" title=" nanostructure"> nanostructure</a>, <a href="https://publications.waset.org/abstracts/search?q=oxidation%20potential" title=" oxidation potential"> oxidation potential</a>, <a href="https://publications.waset.org/abstracts/search?q=solar%20energy" title=" solar energy"> solar energy</a> </p> <a href="https://publications.waset.org/abstracts/83510/synthesis-and-application-of-an-organic-dye-in-nanostructure-solar-cells-device" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/83510.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">193</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2196</span> The Effects of Zinc Oxide Nanoparticles Loaded with Indole-3-Acetic Acid and Indole-3-Butyric Acid on in vitro Rooting of Apple Microcuttings</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shabnam%20Alizadeh">Shabnam Alizadeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Hatice%20Dumanoglu"> Hatice Dumanoglu </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Plant tissue culture is a substantial plant propagation technique for mass clonal production throughout the year, regardless of time in fruit species. However, the rooting achievement must be enhanced in the difficult-to-root genotypes. Classical auxin applications in clonal propagation of these genotypes are inadequate to solve the rooting problem. Nanoparticles having different physical and chemical properties from bulk material could enhance the rooting success of controlled release of these substances when loaded with auxin due to their ability to reach the active substance up to the target cells as a carrier system.The purpose of this study is to investigate the effects of zinc oxide nanoparticles loaded with indole-3-acetic acid (IAA-nZnO) and indole-3-butyric acid (IBA-nZnO) on in vitro rooting of microcuttings in a difficult-to-root apple genotype (Malus domestica Borkh.). Rooting treatments consisted of IBA or IAA at concentrations of 0.5, 1.0, 2.0, 3.0 mg/L; nZnO, IAA-nZnO and IBA-nZnO at doses of 0.0, 1.0, 2.0, 3.0, 4.0, 5.0, 6.0 mg/L were used. All components were added to the Murashige and Skoog (MS) basal medium at strength ½ with 2% sucrose and 0.7% agar before autoclaving. In the study, no rooting occurred in control and nZnO applications. Especially, 1.0 mg/L and 2.0 mg/L IBA-nZnO nanoparticle applications (containing 0.5 mg/L and 0.9 mg/L IBA), respectively with rooting rates of 40.3% and 70.4%, rooting levels of 2.0±0.4 and 2.3±0.4, 2.6±0.7 and 2.5±0.6 average root numbers and 20.4±1.6 mm and 20.2±3.4 mm average root lengths put forward as effective applications. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Auxin" title="Auxin">Auxin</a>, <a href="https://publications.waset.org/abstracts/search?q=Malus" title=" Malus"> Malus</a>, <a href="https://publications.waset.org/abstracts/search?q=nanotechnology" title=" nanotechnology"> nanotechnology</a>, <a href="https://publications.waset.org/abstracts/search?q=zinc%20oxide%20nanoparticles" title=" zinc oxide nanoparticles"> zinc oxide nanoparticles</a> </p> <a href="https://publications.waset.org/abstracts/124807/the-effects-of-zinc-oxide-nanoparticles-loaded-with-indole-3-acetic-acid-and-indole-3-butyric-acid-on-in-vitro-rooting-of-apple-microcuttings" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/124807.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">144</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2195</span> Protoplast Cultures of Murraya paniculata L. Jack and Their Regeneration into Plant Precocious Flowering</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hasan%20Basri%20Jumin">Hasan Basri Jumin</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Protoplasts isolated from embryogenic callus of Murraya paniculata (L. Jack.) were cultured in MT (Murashige and Tucker, 1969) basal medium containing 5% sucrose supplemented with kinetin, malt extract (ME) and 0.6 M sorbitol. About 85% of the surviving protoplasts formed a cell wall within 6 d of culture and the first cell division was observed 7 days after isolation. The highest plating effi¬ciency was obtained on MT basal medium containing 5% sucrose supplemented with 0.01 mg 1-1 kinetin 600 mg 1-1 ME, MT basal medium containing 5% sucrose and supplemented with 0.01 mg 1-1 Indole-acetic-acid (IAA) was found to be a medium suitable for the development somatic embryos into heart-shaped somatic embryos. The highest percentage of shoot formation was obtained using 0.1 mg 1-1 Indole-acitic-acid (IAA) 0..1 mg 1-1 gibberellic acid (GA3). In this investigation 40 plants were survived and grew normally in the soil. After two months maitained in the soil plants formed flower and flower developed into fruits on the soil treated with BA. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=gibberellic-acid" title="gibberellic-acid">gibberellic-acid</a>, <a href="https://publications.waset.org/abstracts/search?q=indole-acetic-acid" title=" indole-acetic-acid"> indole-acetic-acid</a>, <a href="https://publications.waset.org/abstracts/search?q=protoplast" title=" protoplast"> protoplast</a>, <a href="https://publications.waset.org/abstracts/search?q=precocious-flowering" title=" precocious-flowering"> precocious-flowering</a>, <a href="https://publications.waset.org/abstracts/search?q=somatic-embryo" title=" somatic-embryo"> somatic-embryo</a> </p> <a href="https://publications.waset.org/abstracts/45902/protoplast-cultures-of-murraya-paniculata-l-jack-and-their-regeneration-into-plant-precocious-flowering" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/45902.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">345</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2194</span> Indigo Production in a Fed Batch Bioreactor Using Aqueous-Solvent Two Phase System</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Vaishnavi%20Unde">Vaishnavi Unde</a>, <a href="https://publications.waset.org/abstracts/search?q=Srikanth%20Mutnuri"> Srikanth Mutnuri</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Today dye stuff sector is one of the major chemical industries in India. Indigo is a blue coloured dye used all over the world in large quantity. The indigo dye produced and used in textile industries is synthetic having toxic effect, thus there is an increase in interest for natural dyes owing to the environmental concerns. The present study focuses on the use of a strain Pandoraea sp. isolated from garage soil, for the production of indigo in fed batch bioreactor. A comparative study between single phase and two phase production was carried out in this work. The blue colour produced during the experiments was analyzed using, TLC, UV-visible spectrophotometer and FTIR technique. The blue pigment was found to be indigo. The production of bio-indigo was done in a single phase fermentor carrying medium and substrate indole in dissolved form and was found to produce maximum of 0.041 g/L of indigo. Whereas there was an increase in production of indigo to 0.068 g/L in a two phase, water-silicone oil system. In this study the advantage of using second phase as silicone oil has enhanced the indigo production, as the second phase made the substrate available to the bacteria by increasing the surface area as well as it helped to prevent the inhibition effect of the high concentration of substrate, indole. The effect of single and two phases on the growth of bacteria was also studied. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=dyes" title="dyes">dyes</a>, <a href="https://publications.waset.org/abstracts/search?q=fed%20batch%20reactor" title=" fed batch reactor"> fed batch reactor</a>, <a href="https://publications.waset.org/abstracts/search?q=indole" title=" indole"> indole</a>, <a href="https://publications.waset.org/abstracts/search?q=Indigo" title=" Indigo "> Indigo </a> </p> <a href="https://publications.waset.org/abstracts/37269/indigo-production-in-a-fed-batch-bioreactor-using-aqueous-solvent-two-phase-system" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/37269.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">433</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2193</span> Characterization of Fe Doped ZnO Synthesised by Sol-Gel and Combustion Routes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20Ravindiran">M. Ravindiran</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20Shankar"> P. Shankar</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This paper deals with the comparison of two synthesis methods, namely, sol-gel, and combustion to prepare Fe doped ZnO nano material. Characterization results for structural, optical and magnetic properties were analyzed for the sol gel and combustion synthesis derived materials. Magnetic studies of the prepared compounds reveal that the combustion synthesis derived material has good magnetization of 50 emu/gm with a better hysteresis loop curve. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=DMS" title="DMS">DMS</a>, <a href="https://publications.waset.org/abstracts/search?q=combustion" title=" combustion"> combustion</a>, <a href="https://publications.waset.org/abstracts/search?q=ferromagnetic" title=" ferromagnetic"> ferromagnetic</a>, <a href="https://publications.waset.org/abstracts/search?q=synthesis%20methods" title=" synthesis methods"> synthesis methods</a> </p> <a href="https://publications.waset.org/abstracts/28107/characterization-of-fe-doped-zno-synthesised-by-sol-gel-and-combustion-routes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/28107.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">426</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2192</span> High Temperature Volume Combustion Synthesis of Ti3Al with Low Porosities </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nese%20%20Ozturk%20Korpe">Nese Ozturk Korpe</a>, <a href="https://publications.waset.org/abstracts/search?q=Muhammed%20H.%20Karas"> Muhammed H. Karas</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Reaction synthesis, or combustion synthesis, is a processing technique in which the thermal activation energy of formation of a compound is sustained by its exothermic heat of reaction. The aim of the present study was to investigate the effect of high initial pressing pressures (420 MPa, 630 MPa, and 850 MPa) on porosity of Ti3Al which produced by volume combustion synthesis. Microstructure examinations were performed by optical microscope (OM) and scanning electron microscope (SEM). Phase analyses were performed with X-ray diffraction device (XRD). A significant decrease in porosity was obtained due to an increase in the initial pressing pressure. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Titanium%20Aluminide" title="Titanium Aluminide">Titanium Aluminide</a>, <a href="https://publications.waset.org/abstracts/search?q=Volume%20Combustion%20Synthesis" title=" Volume Combustion Synthesis"> Volume Combustion Synthesis</a>, <a href="https://publications.waset.org/abstracts/search?q=Intermetallic" title=" Intermetallic"> Intermetallic</a>, <a href="https://publications.waset.org/abstracts/search?q=Porosity" title=" Porosity"> Porosity</a> </p> <a href="https://publications.waset.org/abstracts/120337/high-temperature-volume-combustion-synthesis-of-ti3al-with-low-porosities" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/120337.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">171</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2191</span> Efficient Synthesis of Highly Functionalized Biologically Important Spirocarbocyclic Oxindoles via Hauser Annulation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kanduru%20Lokesh">Kanduru Lokesh</a>, <a href="https://publications.waset.org/abstracts/search?q=Venkitasamy%20Kesavan"> Venkitasamy Kesavan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The unique structural features of spiro-oxindoles with diverse biological activities have made them privileged structures in new drug discovery. The key structural characteristic of these compounds is the spiro ring fused at the C-3 position of the oxindole core with varied heterocyclic motifs. Structural diversification of heterocyclic scaffolds to synthesize new chemical entities as pharmaceuticals and agrochemicals is one of the important goals of synthetic organic chemists. Nitrogen and oxygen containing heterocycles are by far the most widely occurring privileged structures in medicinal chemistry. The structural complexity and distinct three-dimensional arrangement of functional groups of these privileged structures are generally responsible for their specificity against biological targets. Structurally diverse compound libraries have proved to be valuable assets for drug discovery against challenging biological targets. Thus, identifying a new combination of substituents at C-3 position on oxindole moiety is of great importance in drug discovery to improve the efficiency and efficacy of the drugs. The development of suitable methodology for the synthesis of spiro-oxindole compounds has attracted much interest often in response to the significant biological activity displayed by the both natural and synthetic compounds. So creating structural diversity of oxindole scaffolds is need of the decade and formidable challenge. A general way to improve synthetic efficiency and also to access diversified molecules is through the annulation reactions. Annulation reactions allow the formation of complex compounds starting from simple substrates in a single transformation consisting of several steps in an ecologically and economically favorable way. These observations motivated us to develop the annulation reaction protocol to enable the synthesis of a new class of spiro-oxindole motifs which in turn would enable the enhancement of molecular diversity. As part of our enduring interest in the development of novel, efficient synthetic strategies to enable the synthesis of biologically important oxindole fused spirocarbocyclic systems, We have developed an efficient methodology for the construction of highly functionalized spirocarbocyclic oxindoles through [4+2] annulation of phthalides via Hauser annulation. functionalized spirocarbocyclic oxindoles was accomplished for the first time in the literature using Hauser annulation strategy. The reaction between methyleneindolinones and arylsulfonylphthalides catalyzed by cesium carbonate led to the access of new class of biologically important spiro[indoline-3,2'-naphthalene] derivatives in very good yields. The synthetic utility of the annulated product was further demonstrated by fluorination Using NFSI as a fluorinating agent to furnish corresponding fluorinated product. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hauser-Kraus%20annulation" title="Hauser-Kraus annulation">Hauser-Kraus annulation</a>, <a href="https://publications.waset.org/abstracts/search?q=spiro%20carbocyclic%20oxindoles" title=" spiro carbocyclic oxindoles"> spiro carbocyclic oxindoles</a>, <a href="https://publications.waset.org/abstracts/search?q=oxindole-ester" title=" oxindole-ester"> oxindole-ester</a>, <a href="https://publications.waset.org/abstracts/search?q=fluoridation" title=" fluoridation"> fluoridation</a> </p> <a href="https://publications.waset.org/abstracts/78629/efficient-synthesis-of-highly-functionalized-biologically-important-spirocarbocyclic-oxindoles-via-hauser-annulation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/78629.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">198</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2190</span> Synthesis and Characterization of Cyclic PNC-28 Peptide, Residues 17–26 (ETFSDLWKLL), A Binding Domain of p53</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Deepshikha%20Verma">Deepshikha Verma</a>, <a href="https://publications.waset.org/abstracts/search?q=V.%20N.%20Rajasekharan%20Pillai"> V. N. Rajasekharan Pillai</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The present study reports the synthesis of cyclic PNC-28 peptides with solid-phase peptide synthesis method. In the first step, we synthesize the linear PNC-28 Peptide and in the second step, we cyclize (N-to-C or head-to-tail cyclization) the linear PNC-28 peptide. The molecular formula of cyclic PNC-28 peptide is C64H88N12O16 and its m/z mass is ≈1233.64. Elemental analysis of cyclic PNC-28 is C, 59.99; H, 6.92; N, 13.12; O, 19.98. The characterization of LC-MS, CD, FT-IR, and 1HNMR has been done to confirm the successful synthesis and cyclization of linear PNC-28 peptides. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=CD" title="CD">CD</a>, <a href="https://publications.waset.org/abstracts/search?q=FTIR" title=" FTIR"> FTIR</a>, <a href="https://publications.waset.org/abstracts/search?q=1HNMR" title=" 1HNMR"> 1HNMR</a>, <a href="https://publications.waset.org/abstracts/search?q=cyclic%20peptide" title=" cyclic peptide"> cyclic peptide</a> </p> <a href="https://publications.waset.org/abstracts/149263/synthesis-and-characterization-of-cyclic-pnc-28-peptide-residues-17-26-etfsdlwkll-a-binding-domain-of-p53" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/149263.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">130</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2189</span> Zinc Borate Synthesis Using Hydrozincite and Boric Acid with Ultrasonic Method</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=D.%20S.%20Vardar">D. S. Vardar</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20S.%20Kipcak"> A. S. Kipcak</a>, <a href="https://publications.waset.org/abstracts/search?q=F.%20T.%20Senberber"> F. T. Senberber</a>, <a href="https://publications.waset.org/abstracts/search?q=E.%20M.%20Derun"> E. M. Derun</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Piskin"> S. Piskin</a>, <a href="https://publications.waset.org/abstracts/search?q=N.%20Tugrul"> N. Tugrul</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Zinc borate is an important inorganic hydrate borate material, which can be use as a flame retardant agent and corrosion resistance material. This compound can loss its structural water content at higher than 290°C. Due to thermal stability; Zinc Borate can be used as flame reterdant at high temperature process of plastic and gum. In this study, the ultrasonic reaction of zinc borates were studied using hydrozincite (Zn5(CO3)2•(OH)6) and boric acid (H3BO3) raw materials. Before the synthesis raw materials were characterized by X-Ray Diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FT-IR). Ultrasonic method is a new application on the zinc borate synthesis. The synthesis parameters were set to 90°C reaction temperature and 55 minutes of reaction time, with 1:1, 1:2, 1:3, 1:4 and 1:5 molar ratio of starting materials (Zn5(CO3)2•(OH)6 : H3BO3). After the zinc borate synthesis, the products analyzed by XRD and FT-IR. As a result, optimum molar ratio of 1:5 (Zn5(CO3)2•(OH)6:H3BO3) is determined for the synthesis of zinc borates with ultrasonic method. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=borate" title="borate">borate</a>, <a href="https://publications.waset.org/abstracts/search?q=ultrasonic%20method" title=" ultrasonic method"> ultrasonic method</a>, <a href="https://publications.waset.org/abstracts/search?q=zinc%20borate" title=" zinc borate"> zinc borate</a>, <a href="https://publications.waset.org/abstracts/search?q=zinc%20borate%20synthesis" title=" zinc borate synthesis"> zinc borate synthesis</a> </p> <a href="https://publications.waset.org/abstracts/32481/zinc-borate-synthesis-using-hydrozincite-and-boric-acid-with-ultrasonic-method" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/32481.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">407</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2188</span> Rauvolfine B Isolated from the Bark of Rauvolfia reflexa (Apocynaceae) Induces Apoptosis through Activation of Caspase-9 Coupled with S Phase Cell Cycle Arrest</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mehran%20Fadaeinasab">Mehran Fadaeinasab</a>, <a href="https://publications.waset.org/abstracts/search?q=Hamed%20Karimian"> Hamed Karimian</a>, <a href="https://publications.waset.org/abstracts/search?q=Najihah%20Mohd%20Hashim"> Najihah Mohd Hashim</a>, <a href="https://publications.waset.org/abstracts/search?q=Hapipah%20Mohd%20Ali"> Hapipah Mohd Ali </a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, three indole alkaloids namely; rauvolfine B, macusine B, and isoreserpiline have been isolated from the dichloromethane crude extract of Rauvolfia reflexa bark (Apocynaceae). The structural elucidation of the isolated compounds has been performed using spectral methods such as UV, IR, MS, 1D, and 2D NMR. Rauvolfine B showed anti proliferation activity on HCT-116 cancer cell line, its cytotoxicity induction was observed using MTT assay in eight different cell lines. Annexin-V is serving as a marker for apoptotic cells and the Annexin-V-FITC assay was carried out to observe the detection of cell-surface Phosphatidylserine (PS). Apoptosis was confirmed by using caspase-8 and -9 assays. Cell cycle arrest was also investigated using flowcytometric analysis. rauvolfine B had exhibited significantly higher cytotoxicity against HCT-116 cell line. The treatment significantly arrested HCT-116 cells in the S phase. Together, the results presented in this study demonstrated that rauvolfine B inhibited the proliferation of HCT-116 cells and programmed cell death followed by cell cycle arrest. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=apocynacea" title="apocynacea">apocynacea</a>, <a href="https://publications.waset.org/abstracts/search?q=indole%20alkaloid" title=" indole alkaloid"> indole alkaloid</a>, <a href="https://publications.waset.org/abstracts/search?q=apoptosis" title=" apoptosis"> apoptosis</a>, <a href="https://publications.waset.org/abstracts/search?q=cell%20cycle%20arrest" title=" cell cycle arrest"> cell cycle arrest</a> </p> <a href="https://publications.waset.org/abstracts/13403/rauvolfine-b-isolated-from-the-bark-of-rauvolfia-reflexa-apocynaceae-induces-apoptosis-through-activation-of-caspase-9-coupled-with-s-phase-cell-cycle-arrest" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/13403.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">334</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2187</span> Computer-Aided Drug Repurposing for Mycobacterium Tuberculosis by Targeting Tryptophanyl-tRNA Synthetase</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Neslihan%20Demirci">Neslihan Demirci</a>, <a href="https://publications.waset.org/abstracts/search?q=Serdar%20Durda%C4%9F%C4%B1"> Serdar Durdağı</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Mycobacterium tuberculosis is still a worldwide disease-causing agent that, according to WHO, led to the death of 1.5 million people from tuberculosis (TB) in 2020. The bacteria reside in macrophages located specifically in the lung. There is a known quadruple drug therapy regimen for TB consisting of isoniazid (INH), rifampin (RIF), pyrazinamide (PZA), and ethambutol (EMB). Over the past 60 years, there have been great contributions to treatment options, such as recently approved delamanid (OPC67683) and bedaquiline (TMC207/R207910), targeting mycolic acid and ATP synthesis, respectively. Also, there are natural compounds that can block the tryptophanyl-tRNA synthetase (TrpRS) enzyme, chuangxinmycin, and indolmycin. Yet, already the drug resistance is reported for those agents. In this study, the newly released TrpRS enzyme structure is investigated for potential inhibitor drugs from already synthesized molecules to help the treatment of resistant cases and to propose an alternative drug for the quadruple drug therapy of tuberculosis. Maestro, Schrodinger is used for docking and molecular dynamic simulations. In-house library containing ~8000 compounds among FDA-approved indole-containing compounds, a total of 57 obtained from the ChemBL were used for both ATP and tryptophan binding pocket docking. Best of indole-containing 57 compounds were subjected to hit expansion and compared later with virtual screening workflow (VSW) results. After docking, VSW was done. Glide-XP docking algorithm was chosen. When compared, VSW alone performed better than the hit expansion module. Best scored compounds were kept for ten ns molecular dynamic simulations by Desmond. Further, 100 ns molecular dynamic simulation was performed for elected molecules according to Z-score. The top three MMGBSA-scored compounds were subjected to steered molecular dynamic (SMD) simulations by Gromacs. While SMD simulations are still being conducted, ponesimod (for multiple sclerosis), vilanterol (β₂ adrenoreceptor agonist), and silodosin (for benign prostatic hyperplasia) were found to have a significant affinity for tuberculosis TrpRS, which is the propulsive force for the urge to expand the research with in vitro studies. Interestingly, top-scored ponesimod has been reported to have a side effect that makes the patient prone to upper respiratory tract infections. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=drug%20repurposing" title="drug repurposing">drug repurposing</a>, <a href="https://publications.waset.org/abstracts/search?q=molecular%20dynamics" title=" molecular dynamics"> molecular dynamics</a>, <a href="https://publications.waset.org/abstracts/search?q=tryptophanyl-tRNA%20synthetase" title=" tryptophanyl-tRNA synthetase"> tryptophanyl-tRNA synthetase</a>, <a href="https://publications.waset.org/abstracts/search?q=tuberculosis" title=" tuberculosis"> tuberculosis</a> </p> <a href="https://publications.waset.org/abstracts/150174/computer-aided-drug-repurposing-for-mycobacterium-tuberculosis-by-targeting-tryptophanyl-trna-synthetase" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/150174.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">123</span> </span> </div> </div> <ul class="pagination"> <li class="page-item disabled"><span class="page-link">&lsaquo;</span></li> <li class="page-item active"><span class="page-link">1</span></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis&page=3">3</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis&page=4">4</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis&page=5">5</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis&page=6">6</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis&page=7">7</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis&page=8">8</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis&page=9">9</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=indole%20and%20indoline%20synthesis&page=10">10</a></li> <li class="page-item disabled"><span class="page-link">...</span></li> <li class="page-item"><a class="page-link" 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