rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
9
|
pubmed:dateCreated |
2001-5-16
|
pubmed:abstractText |
The significant contribution of folded conformation (2) of the anxiolytic tandospirone (1) in aqueous solution was verified by dynamic 1H NMR. A structurally rigid mimic of 2 was designed and synthesized to evaluate the implication of 2 towards neuroleptic receptor binding. The designed structures provided a new rigid scaffold for dopamine D4 ligands.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Indicators and Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Isoindoles,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Piperazines,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidines,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D4,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Serotonin, 5-HT1,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin Receptor Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Solutions,
http://linkedlifedata.com/resource/pubmed/chemical/tandospirone
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0960-894X
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
7
|
pubmed:volume |
11
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1141-4
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:11354362-Drug Design,
pubmed-meshheading:11354362-Indicators and Reagents,
pubmed-meshheading:11354362-Isoindoles,
pubmed-meshheading:11354362-Kinetics,
pubmed-meshheading:11354362-Ligands,
pubmed-meshheading:11354362-Magnetic Resonance Spectroscopy,
pubmed-meshheading:11354362-Models, Molecular,
pubmed-meshheading:11354362-Molecular Conformation,
pubmed-meshheading:11354362-Molecular Mimicry,
pubmed-meshheading:11354362-Piperazines,
pubmed-meshheading:11354362-Pyrimidines,
pubmed-meshheading:11354362-Receptors, Dopamine D2,
pubmed-meshheading:11354362-Receptors, Dopamine D4,
pubmed-meshheading:11354362-Receptors, Serotonin,
pubmed-meshheading:11354362-Receptors, Serotonin, 5-HT1,
pubmed-meshheading:11354362-Serotonin Receptor Agonists,
pubmed-meshheading:11354362-Solutions
|
pubmed:year |
2001
|
pubmed:articleTitle |
Conformational analysis of tandospirone in aqueous solution: lead evolution of potent dopamine D4 receptor ligands.
|
pubmed:affiliation |
Sumitomo Pharmaceuticals Research Division, Osaka, Japan.
|
pubmed:publicationType |
Journal Article
|