rdf:type |
|
lifeskim:mentions |
umls-concept:C0020792,
umls-concept:C0031957,
umls-concept:C0038477,
umls-concept:C0063510,
umls-concept:C0205314,
umls-concept:C0205430,
umls-concept:C0243072,
umls-concept:C0243076,
umls-concept:C0332256,
umls-concept:C0456387,
umls-concept:C0597357,
umls-concept:C0679622
|
pubmed:issue |
21
|
pubmed:dateCreated |
2002-10-9
|
pubmed:abstractText |
Optimization of the lead compound 2-[-4-(4-chloro-benzyl)-piperazin-1-yl]-1-(2,3-dihydro-indol-1-yl)-ethanone 1 by systematic structure-activity relation (SAR) studies lead to two potent compounds 2-[-4-(4-chloro-benzyl)-piperazin-1-yl]-1-(2-methy-2,3-dihydro-indol-1-yl)-ethanone 2n and 2-[-4-(4-chloro-benzyl)-piperazin-1-yl]-1-(2-methy-2,3-dihydro-indol-1-yl)-ethanone 7b. Their related synthesis was also reported.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DRD4 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Dopamine Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Drd4 protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Glycine,
http://linkedlifedata.com/resource/pubmed/chemical/Indoles,
http://linkedlifedata.com/resource/pubmed/chemical/Piperazines,
http://linkedlifedata.com/resource/pubmed/chemical/Prazosin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D4,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0960-894X
|
pubmed:author |
pubmed-author:BrodbeckRobbinR,
pubmed-author:HeXiaoshuX,
pubmed-author:HodgettsKevinK,
pubmed-author:HutchisonAlanA,
pubmed-author:KieltykaAndrzejA,
pubmed-author:KoverRenata XRX,
pubmed-author:PetersonJohnJ,
pubmed-author:PrimusReneeR,
pubmed-author:RachwalStanislawS,
pubmed-author:ThurkaufAndrewA,
pubmed-author:WasleyJan W FJW,
pubmed-author:ZhangXiaoyanX,
pubmed-author:ZhaoHeH
|
pubmed:issnType |
Print
|
pubmed:day |
4
|
pubmed:volume |
12
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
3105-9
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:12372512-Animals,
pubmed-meshheading:12372512-Binding, Competitive,
pubmed-meshheading:12372512-Dopamine Antagonists,
pubmed-meshheading:12372512-Glycine,
pubmed-meshheading:12372512-Humans,
pubmed-meshheading:12372512-Indoles,
pubmed-meshheading:12372512-Piperazines,
pubmed-meshheading:12372512-Prazosin,
pubmed-meshheading:12372512-Rats,
pubmed-meshheading:12372512-Receptors, Dopamine D2,
pubmed-meshheading:12372512-Receptors, Dopamine D4,
pubmed-meshheading:12372512-Recombinant Proteins,
pubmed-meshheading:12372512-Structure-Activity Relationship
|
pubmed:year |
2002
|
pubmed:articleTitle |
Indoline and piperazine containing derivatives as a novel class of mixed D(2)/D(4) receptor antagonists. Part 1: identification and structure-activity relationships.
|
pubmed:affiliation |
Neurogen Corporation, 35Northeast Industrial Road, Branford, CT 06405, USA. hzhao@nrgn.com
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pubmed:publicationType |
Journal Article,
In Vitro
|