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About: Cabergoline

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title="Switch to /sparql endpoint"><i class="bi-box-arrow-up-right"></i> Sparql Endpoint </a> </li> </ul> </div> </div> </nav> <div style="margin-bottom: 60px"></div> <!-- /navbar --> <!-- page-header --> <section> <div class="container-xl"> <div class="row"> <div class="col"> <h1 id="title" class="display-6"><b>About:</b> <a href="http://dbpedia.org/resource/Cabergoline">Cabergoline</a> </h1> </div> </div> <div class="row"> <div class="col"> <div class="text-muted"> <span class="text-nowrap">An Entity of Type: <a href="http://dbpedia.org/ontology/ChemicalSubstance">chemical substance</a>, </span> <span class="text-nowrap">from Named Graph: <a href="http://dbpedia.org">http://dbpedia.org</a>, </span> <span class="text-nowrap">within Data Space: <a href="http://dbpedia.org">dbpedia.org</a></span> </div> </div> </div> <div class="row pt-2"> <div class="col-xs-9 col-sm-10"> <p class="lead">Cabergoline, sold under the brand name Dostinex among others, is a dopaminergic medication used in the treatment of high prolactin levels, prolactinomas, Parkinson&#39;s disease, and for other indications. It is taken by mouth. Cabergoline is an ergot derivative and a potent dopamine D2 receptor agonist. Cabergoline was patented in 1980 and approved for medical use in 1993.</p> </div> <div class="col-xs-3 col-sm-2"> <a href="#" class="thumbnail"> <img src="http://commons.wikimedia.org/wiki/Special:FilePath/Cabergoline.svg?width=300" alt="thumbnail" class="img-fluid" /> </a> </div> </div> </div> </section> <!-- page-header --> <!-- property-table --> <section> <div class="container-xl"> <div class="row"> <div class="table-responsive"> <table class="table table-hover table-sm table-light"> <thead> <tr> <th class="col-xs-3 ">Property</th> <th class="col-xs-9 px-3">Value</th> </tr> </thead> <tbody> <tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/ontology/abstract"><small>dbo:</small>abstract</a> </td><td class="col-10 text-break"><ul> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="ar" >كابرجولين (الأسماء التجارية Caberlin, Dostinex and Cabaser)، من مشتقات فطر الارغوت، وهو ناهض قوي يعمل على مستقبلات الدوبامين D2. وقد بينت الدراسات على الفئران أنالكابرجولين له تأثيرمباشر مثبط على خلايا لاكتوتروف الموجودة بالغدة النخامية (البرولاكتين). وكثيراً ما يستخدم كخط العلاج الأول لأورام الغدة النخامية التي تفرزالبرولاكتين (البرولاكتينوماس) بسبب قوة التجاذب بينه وبين مستقبلات D2 وأيضاً قلة حدة آثارها الجانبية وملاءمة جدول الجرعات مقارنة بالبروموكريبتين الذي كان يستخدم سابقاً.</span><small> (ar)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="de" >Cabergolin ist ein von Mutterkornalkaloiden abgeleiteter Arzneistoff. Er wirkt als primärer Dopamin-D2-Agonist. Cabergolin wird in der Humanmedizin als Mittel gegen Morbus Parkinson, zum Abstillen und bei Galaktorrhoe oder bei Prolaktin-Überschuss angewendet. In der Tiermedizin wird der Wirkstoff bei Scheinträchtigkeit, zur Aborteinleitung, zur Östruseinleitung, bei Mammatumoren und zur Pyometratherapie eingesetzt.</span><small> (de)</small></span></li> <li><span class="literal"><span property="dbo:abstract" lang="en" >Cabergoline, sold under the brand name Dostinex among others, is a dopaminergic medication used in the treatment of high prolactin levels, prolactinomas, Parkinson&#39;s disease, and for other indications. It is taken by mouth. Cabergoline is an ergot derivative and a potent dopamine D2 receptor agonist. Cabergoline was patented in 1980 and approved for medical use in 1993.</span><small> (en)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="es" >La cabergolina o cabergoline​ es una ergolina agonista de los receptores de dopamina tipo D2, D3 y también del receptor 5-HT2B de serotonina. Se utiliza para el tratamiento de la hiperprolactinemia de cualquier origen, así como de la enfermedad de Parkinson, el síndrome de hiperestimulación ovárico, la enfermedad de Cushing y el síndrome de piernas inquietas.​​ Actúa en los receptores de dopamina de las del hipotálamo, donde suprime la producción de prolactina en la hipófisis. También se une a los receptores D2 del cuerpo estriado imitando las acciones de la dopamina en el control motor.​</span><small> (es)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="fr" >La cabergoline est un dérivé de l&#39;ergot du seigle, agissant comme agoniste dopaminergique. L&#39;administration de cette molécule comme agent antiparkinsonien se transforme en un traitement de deuxième ligne (après l&#39;utilisation d&#39;agents non dérivés de l&#39;ergot). Au Japon en 2007, des études montrent un lien entre l&#39;utilisation de ces agents dérivés de l&#39;ergot du seigle et des valvulopathies cardiaques.</span><small> (fr)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="it" >La cabergolina è un derivato dell&#39;ergot, che funziona come agonista dei recettori D2 della dopamina. Il principio attivo si utilizza contro la malattia di Parkinson in aggiunta alla levodopa. Alcuni studi sui ratti hanno dimostrato che la cabergolina ha un effetto inibitorio diretto sulle cellule dell’ipofisi che producono l&#39;ormone prolattina. Viene usata come farmaco di prima scelta nella gestione dei prolattinomi, grazie alla sua affinità per i recettori D2, e grazie agli effetti collaterali meno gravi e un dosaggio più conveniente rispetto alla vecchia bromocriptina. È stata brevettata nel 1980 e approvata per uso medico nel 1993.</span><small> (it)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="pt" >Cabergolina é um fármaco agonista dopaminérgico derivado do ergot, fungo contaminante comum do centeio e outros cereais, ou pelo uso excessivo ou mal orientado de drogas derivadas da ergolina. com longa ação, utilizado como inibidor da secreção de leite, bloqueando a prolactina.É derivado da cravagem dos cereais e agonista dopaminérgico.</span><small> (pt)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="pl" >Kabergolina (łac. Cabergolinum) – organiczny związek chemiczny, pochodna alkaloidów sporyszu, stosowana głównie w leczeniu hiperprolaktynemii.</span><small> (pl)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="sv" >Kabergolin (IUPAC-namn: N-[3-(dimetylamino)propyl]-N-[(etylamino)karbonyl]-6-(2-propenyl)-8g-ergolin-8-karboxamid, summaformel C26H37N5O2) är en dopaminagonist, med hög affinitet för dopamin D2 receptorer, som används vid behandling av symptomen vid Parkinsons sjukdom. Kabergolin används även för att förhindra laktation (bildandet av bröstmjölk) genom att minska hormonet prolaktin Kemiskt namn: 1-[(6aR,9R,10aR)-7-Allyl-4,6,6a,7,8,9,10,10a-oktahydroindolo[4,3-fg]kinolin-9-karbonyl]-1-[3-(dimetylamino)propyl]-3-etylkarbamid Aktuella läkemedel innehållande Kabergolin finns på Fass. Kabergolin framställdes ursprungligen av läkemedelsföretaget Pfizer.</span><small> (sv)</small></span></li> <li style="display:none;"><span class="literal"><span property="dbo:abstract" lang="uk" >Каберголін (англ. Cabergoline, лат. Cabergolinum) — напівсинтетичний препарат, який є похідним алкалоїду ріжків ерголіну та належить до групи стимуляторів дофамінових рецепторів, та антагоністів пролактину. Каберголін застосовується перорально. Препарат застосовується для лікування низки захворювань, у тому числі , пролактинзалежному безплідді, галактореї, пролактинсекретуючій аденомі гіпофіза, акромегалії, при пролактинзалежній імпотенції, зниженні лібідо, а також для лікування паркінсонізму, та припинення фізіологічної лактації після пологів. Каберголін уперше синтезований у лабораторії італійської компанії , та запатентований у 1982 році.</span><small> (uk)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/ontology/alternativeName"><small>dbo:</small>alternativeName</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbo:alternativeName" lang="en" >Dostinex, others</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/ontology/casNumber"><small>dbo:</small>casNumber</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbo:casNumber" >81409-90-7</span></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/ontology/chEBI"><small>dbo:</small>chEBI</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbo:chEBI" >3286</span></span></li> 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href="http://dbpedia.org/resource/Α1D-Adrenergic_receptor"><small>dbr</small>:Α1D-Adrenergic_receptor</a></span></li> <li><span class="literal"><a class="uri" rel="dbo:wikiPageWikiLink" resource="http://dbpedia.org/resource/Α2-adrenergic" href="http://dbpedia.org/resource/Α2-adrenergic"><small>dbr</small>:Α2-adrenergic</a></span></li> <li><span class="literal"><a class="uri" rel="dbo:wikiPageWikiLink" resource="http://dbpedia.org/resource/Α2A-Adrenergic_receptor" href="http://dbpedia.org/resource/Α2A-Adrenergic_receptor"><small>dbr</small>:Α2A-Adrenergic_receptor</a></span></li> <li><span class="literal"><a class="uri" rel="dbo:wikiPageWikiLink" resource="http://dbpedia.org/resource/Α2B-Adrenergic_receptor" href="http://dbpedia.org/resource/Α2B-Adrenergic_receptor"><small>dbr</small>:Α2B-Adrenergic_receptor</a></span></li> <li><span class="literal"><a class="uri" rel="dbo:wikiPageWikiLink" resource="http://dbpedia.org/resource/Α2C-Adrenergic_receptor" href="http://dbpedia.org/resource/Α2C-Adrenergic_receptor"><small>dbr</small>:Α2C-Adrenergic_receptor</a></span></li> <li><span class="literal"><a class="uri" rel="dbo:wikiPageWikiLink" resource="http://dbpedia.org/resource/Α2D-Adrenergic_receptor" href="http://dbpedia.org/resource/Α2D-Adrenergic_receptor"><small>dbr</small>:Α2D-Adrenergic_receptor</a></span></li> <li><span class="literal"><a class="uri" rel="dbo:wikiPageWikiLink" resource="http://dbpedia.org/resource/Β1-Adrenergic_receptor" href="http://dbpedia.org/resource/Β1-Adrenergic_receptor"><small>dbr</small>:Β1-Adrenergic_receptor</a></span></li> <li><span class="literal"><a class="uri" rel="dbo:wikiPageWikiLink" resource="http://dbpedia.org/resource/Β2-Adrenergic_receptor" href="http://dbpedia.org/resource/Β2-Adrenergic_receptor"><small>dbr</small>:Β2-Adrenergic_receptor</a></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/atcPrefix"><small>dbp:</small>atcPrefix</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:atcPrefix" lang="en" >G02</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/atcSuffix"><small>dbp:</small>atcSuffix</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:atcSuffix" lang="en" >CB03</span><small> (en)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/bioavailability"><small>dbp:</small>bioavailability</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:bioavailability" lang="en" >First-pass effect seen; absolute bioavailability unknown</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/c"><small>dbp:</small>c</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:c" datatype="xsd:integer" >26</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/casNumber"><small>dbp:</small>casNumber</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:casNumber" datatype="xsd:integer" >81409</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/chebi"><small>dbp:</small>chebi</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:chebi" datatype="xsd:integer" >3286</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/chembl"><small>dbp:</small>chembl</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:chembl" datatype="xsd:integer" >1201087</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/chemspiderid"><small>dbp:</small>chemspiderid</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:chemspiderid" datatype="xsd:integer" >49452</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/drugbank"><small>dbp:</small>drugbank</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:drugbank" lang="en" >DB00248</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/eliminationHalfLife"><small>dbp:</small>eliminationHalfLife</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:eliminationHalfLife" datatype="dbd:second" >-248400.0</span></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/excretion"><small>dbp:</small>excretion</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:excretion" lang="en" >Urine , feces</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/h"><small>dbp:</small>h</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:h" datatype="xsd:integer" >37</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/iupacName"><small>dbp:</small>iupacName</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:iupacName" lang="en" >-N-[3-propyl]-N--7-prop-2-enyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/iupharLigand"><small>dbp:</small>iupharLigand</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:iupharLigand" datatype="xsd:integer" >37</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/kegg"><small>dbp:</small>kegg</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:kegg" lang="en" >D00987</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/legalUs"><small>dbp:</small>legalUs</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:legalUs" lang="en" >Rx-only</span><small> (en)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/licenceUs"><small>dbp:</small>licenceUs</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:licenceUs" lang="en" >CABERGOLINE</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/metabolism"><small>dbp:</small>metabolism</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:metabolism" lang="en" >Hepatic, predominately via hydrolysis of the acylurea bond or the urea moiety</span><small> (en)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/n"><small>dbp:</small>n</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:n" datatype="xsd:integer" >5</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/o"><small>dbp:</small>o</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:o" datatype="xsd:integer" >2</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/pregnancyUs"><small>dbp:</small>pregnancyUs</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:pregnancyUs" lang="en" >B</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/proteinBound"><small>dbp:</small>proteinBound</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:proteinBound" lang="en" >Moderately bound ; concentration-independent</span><small> (en)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/pubchem"><small>dbp:</small>pubchem</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:pubchem" datatype="xsd:integer" >54746</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/routesOfAdministration"><small>dbp:</small>routesOfAdministration</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><a class="uri" rel="dbp:routesOfAdministration" resource="http://dbpedia.org/resource/Oral_administration" href="http://dbpedia.org/resource/Oral_administration"><small>dbr</small>:Oral_administration</a></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/smiles"><small>dbp:</small>smiles</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:smiles" lang="en" >[H][C@]12C[C@@H]CN[C@]1Cc3c[nH]c4cccc2c34</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/stdinchi"><small>dbp:</small>stdinchi</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:stdinchi" datatype="xsd:integer" >1</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/stdinchikey"><small>dbp:</small>stdinchikey</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:stdinchikey" lang="en" >KORNTPPJEAJQIU-KJXAQDMKSA-N</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/title"><small>dbp:</small>title</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><a class="uri" rel="dbp:title" resource="http://dbpedia.org/resource/Pharmacodynamics" href="http://dbpedia.org/resource/Pharmacodynamics"><small>dbr</small>:Pharmacodynamics</a></span></li> <li><span class="literal"><span property="dbp:title" lang="en" >Medical uses</span><small> (en)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/titlestyle"><small>dbp:</small>titlestyle</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:titlestyle" lang="en" >background:#ccccff</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/tradename"><small>dbp:</small>tradename</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:tradename" lang="en" >Dostinex, others</span><small> (en)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/unii"><small>dbp:</small>unii</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:unii" lang="en" >LL60K9J05T</span><small> (en)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/verifiedfields"><small>dbp:</small>verifiedfields</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:verifiedfields" lang="en" >changed</span><small> (en)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/verifiedrevid"><small>dbp:</small>verifiedrevid</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:verifiedrevid" datatype="xsd:integer" >477165198</span><small> (xsd:integer)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/watchedfields"><small>dbp:</small>watchedfields</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><span property="dbp:watchedfields" lang="en" >changed</span><small> (en)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" href="http://dbpedia.org/property/wikiPageUsesTemplate"><small>dbp:</small>wikiPageUsesTemplate</a> </td><td class="col-10 text-break"><ul> <li><span class="literal"><a class="uri" rel="dbp:wikiPageUsesTemplate" resource="http://dbpedia.org/resource/Template:Adrenergic_receptor_modulators" href="http://dbpedia.org/resource/Template:Adrenergic_receptor_modulators"><small>dbt</small>:Adrenergic_receptor_modulators</a></span></li> <li><span class="literal"><a class="uri" rel="dbp:wikiPageUsesTemplate" resource="http://dbpedia.org/resource/Template:Citation_needed" href="http://dbpedia.org/resource/Template:Citation_needed"><small>dbt</small>:Citation_needed</a></span></li> <li><span 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style="display:none;"><span class="literal"><span property="rdfs:comment" lang="ar" >كابرجولين (الأسماء التجارية Caberlin, Dostinex and Cabaser)، من مشتقات فطر الارغوت، وهو ناهض قوي يعمل على مستقبلات الدوبامين D2. وقد بينت الدراسات على الفئران أنالكابرجولين له تأثيرمباشر مثبط على خلايا لاكتوتروف الموجودة بالغدة النخامية (البرولاكتين). وكثيراً ما يستخدم كخط العلاج الأول لأورام الغدة النخامية التي تفرزالبرولاكتين (البرولاكتينوماس) بسبب قوة التجاذب بينه وبين مستقبلات D2 وأيضاً قلة حدة آثارها الجانبية وملاءمة جدول الجرعات مقارنة بالبروموكريبتين الذي كان يستخدم سابقاً.</span><small> (ar)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="de" >Cabergolin ist ein von Mutterkornalkaloiden abgeleiteter Arzneistoff. Er wirkt als primärer Dopamin-D2-Agonist. Cabergolin wird in der Humanmedizin als Mittel gegen Morbus Parkinson, zum Abstillen und bei Galaktorrhoe oder bei Prolaktin-Überschuss angewendet. In der Tiermedizin wird der Wirkstoff bei Scheinträchtigkeit, zur Aborteinleitung, zur Östruseinleitung, bei Mammatumoren und zur Pyometratherapie eingesetzt.</span><small> (de)</small></span></li> <li><span class="literal"><span property="rdfs:comment" lang="en" >Cabergoline, sold under the brand name Dostinex among others, is a dopaminergic medication used in the treatment of high prolactin levels, prolactinomas, Parkinson&#39;s disease, and for other indications. It is taken by mouth. Cabergoline is an ergot derivative and a potent dopamine D2 receptor agonist. Cabergoline was patented in 1980 and approved for medical use in 1993.</span><small> (en)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="es" >La cabergolina o cabergoline​ es una ergolina agonista de los receptores de dopamina tipo D2, D3 y también del receptor 5-HT2B de serotonina. Se utiliza para el tratamiento de la hiperprolactinemia de cualquier origen, así como de la enfermedad de Parkinson, el síndrome de hiperestimulación ovárico, la enfermedad de Cushing y el síndrome de piernas inquietas.​​ Actúa en los receptores de dopamina de las del hipotálamo, donde suprime la producción de prolactina en la hipófisis. También se une a los receptores D2 del cuerpo estriado imitando las acciones de la dopamina en el control motor.​</span><small> (es)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="fr" >La cabergoline est un dérivé de l&#39;ergot du seigle, agissant comme agoniste dopaminergique. L&#39;administration de cette molécule comme agent antiparkinsonien se transforme en un traitement de deuxième ligne (après l&#39;utilisation d&#39;agents non dérivés de l&#39;ergot). Au Japon en 2007, des études montrent un lien entre l&#39;utilisation de ces agents dérivés de l&#39;ergot du seigle et des valvulopathies cardiaques.</span><small> (fr)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="pt" >Cabergolina é um fármaco agonista dopaminérgico derivado do ergot, fungo contaminante comum do centeio e outros cereais, ou pelo uso excessivo ou mal orientado de drogas derivadas da ergolina. com longa ação, utilizado como inibidor da secreção de leite, bloqueando a prolactina.É derivado da cravagem dos cereais e agonista dopaminérgico.</span><small> (pt)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="pl" >Kabergolina (łac. Cabergolinum) – organiczny związek chemiczny, pochodna alkaloidów sporyszu, stosowana głównie w leczeniu hiperprolaktynemii.</span><small> (pl)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="uk" >Каберголін (англ. Cabergoline, лат. Cabergolinum) — напівсинтетичний препарат, який є похідним алкалоїду ріжків ерголіну та належить до групи стимуляторів дофамінових рецепторів, та антагоністів пролактину. Каберголін застосовується перорально. Препарат застосовується для лікування низки захворювань, у тому числі , пролактинзалежному безплідді, галактореї, пролактинсекретуючій аденомі гіпофіза, акромегалії, при пролактинзалежній імпотенції, зниженні лібідо, а також для лікування паркінсонізму, та припинення фізіологічної лактації після пологів. Каберголін уперше синтезований у лабораторії італійської компанії , та запатентований у 1982 році.</span><small> (uk)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="it" >La cabergolina è un derivato dell&#39;ergot, che funziona come agonista dei recettori D2 della dopamina. Il principio attivo si utilizza contro la malattia di Parkinson in aggiunta alla levodopa. Alcuni studi sui ratti hanno dimostrato che la cabergolina ha un effetto inibitorio diretto sulle cellule dell’ipofisi che producono l&#39;ormone prolattina. Viene usata come farmaco di prima scelta nella gestione dei prolattinomi, grazie alla sua affinità per i recettori D2, e grazie agli effetti collaterali meno gravi e un dosaggio più conveniente rispetto alla vecchia bromocriptina.</span><small> (it)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:comment" lang="sv" >Kabergolin (IUPAC-namn: N-[3-(dimetylamino)propyl]-N-[(etylamino)karbonyl]-6-(2-propenyl)-8g-ergolin-8-karboxamid, summaformel C26H37N5O2) är en dopaminagonist, med hög affinitet för dopamin D2 receptorer, som används vid behandling av symptomen vid Parkinsons sjukdom. Kabergolin används även för att förhindra laktation (bildandet av bröstmjölk) genom att minska hormonet prolaktin Kemiskt namn: 1-[(6aR,9R,10aR)-7-Allyl-4,6,6a,7,8,9,10,10a-oktahydroindolo[4,3-fg]kinolin-9-karbonyl]-1-[3-(dimetylamino)propyl]-3-etylkarbamid Aktuella läkemedel innehållande Kabergolin finns på Fass.</span><small> (sv)</small></span></li> </ul></td></tr><tr class="odd"><td class="col-2"><a class="uri" href="http://www.w3.org/2000/01/rdf-schema#label"><small>rdfs:</small>label</a> </td><td class="col-10 text-break"><ul> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="ar" >كابرجولين</span><small> (ar)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="de" >Cabergolin</span><small> (de)</small></span></li> <li><span class="literal"><span property="rdfs:label" lang="en" >Cabergoline</span><small> (en)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="es" >Cabergolina</span><small> (es)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="it" >Cabergolina</span><small> (it)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="fr" >Cabergoline</span><small> (fr)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="pl" >Kabergolina</span><small> (pl)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="pt" >Cabergolina</span><small> (pt)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="sv" >Kabergolin</span><small> (sv)</small></span></li> <li style="display:none;"><span class="literal"><span property="rdfs:label" lang="uk" >Каберголін</span><small> (uk)</small></span></li> </ul></td></tr><tr class="even"><td class="col-2"><a class="uri" 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