pubmed-article:18193826 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C0391690 | lld:lifeskim |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C0243076 | lld:lifeskim |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C0205464 | lld:lifeskim |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C0043764 | lld:lifeskim |
pubmed-article:18193826 | lifeskim:mentions | umls-concept:C0243072 | lld:lifeskim |
pubmed-article:18193826 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:18193826 | pubmed:dateCreated | 2008-2-7 | lld:pubmed |
pubmed-article:18193826 | pubmed:abstractText | Ghrelin receptor ligands based on trisubstituted 1,2,4-triazole structure were synthesized and evaluated for their in vitro binding and biological activity. In this study, we explored the replacement of the alpha-aminoisobutyryl moiety by aromatic or heteroaromatic groups. Compounds 5 and 34 acted as potent in vivo antagonists of hexarelin-stimulated food intake. These two compounds did not stimulate growth hormone secretion in rodents and did not antagonize growth hormone secretion induced by hexarelin. | lld:pubmed |
pubmed-article:18193826 | pubmed:language | eng | lld:pubmed |
pubmed-article:18193826 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18193826 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18193826 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18193826 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18193826 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18193826 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18193826 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18193826 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18193826 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18193826 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18193826 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18193826 | pubmed:month | Feb | lld:pubmed |
pubmed-article:18193826 | pubmed:issn | 0022-2623 | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:KtenidesM AMA | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:MartinezJeanJ | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:TorselloAnton... | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:LocatelliVitt... | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:GagneDidierD | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:GalleyrandJea... | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:DemangeLucL | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:FehrentzJean-... | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:MousseauxDelp... | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:SanchezPierre... | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:BergéGilbertG | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:RyanJoanneJ | lld:pubmed |
pubmed-article:18193826 | pubmed:author | pubmed-author:MoulinAlineA | lld:pubmed |
pubmed-article:18193826 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18193826 | pubmed:day | 14 | lld:pubmed |
pubmed-article:18193826 | pubmed:volume | 51 | lld:pubmed |
pubmed-article:18193826 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18193826 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18193826 | pubmed:pagination | 689-93 | lld:pubmed |
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pubmed-article:18193826 | pubmed:meshHeading | pubmed-meshheading:18193826... | lld:pubmed |
pubmed-article:18193826 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18193826 | pubmed:articleTitle | New trisubstituted 1,2,4-triazole derivatives as potent ghrelin receptor antagonists. 3. Synthesis and pharmacological in vitro and in vivo evaluations. | lld:pubmed |
pubmed-article:18193826 | pubmed:affiliation | Institut des Biomolécules Max Mousseron, UMR 5247, CNRS, Universités Montpellier 1, Montpellier 2, Montpellier Cedex 5, France. | lld:pubmed |
pubmed-article:18193826 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18193826 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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