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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
24
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pubmed:dateCreated |
1999-4-5
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pubmed:abstractText |
A set of HIV protease inhibitors represented by compound 2 has previously been described. Structural and conformational analysis of this compound suggested that conformational restriction of the P1/P2 portion of the molecule could lead to a novel set of potent protease inhibitors. Thus, probe compounds 3-7 were designed, synthesized, and found to be potent inhibitors of HIV protease.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
|
pubmed:issn |
0960-894X
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pubmed:author |
pubmed-author:BakerC TCT,
pubmed-author:CourtJ JJJ,
pubmed-author:DeiningerD DDD,
pubmed-author:KimE EEE,
pubmed-author:MICC,
pubmed-author:NovakP MPM,
pubmed-author:PazhanisamySS,
pubmed-author:PorterM DMD,
pubmed-author:RayB ABA,
pubmed-author:SalituroF GFG,
pubmed-author:SchairerW CWC,
pubmed-author:TungR DRD
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
8
|
pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3637-42
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pubmed:dateRevised |
2001-11-13
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pubmed:meshHeading | |
pubmed:year |
1998
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pubmed:articleTitle |
Design and synthesis of novel conformationally restricted HIV protease inhibitors.
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pubmed:affiliation |
Vertex Pharmaceuticals Incorporated, Cambridge, MA 02139, USA.
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pubmed:publicationType |
Journal Article
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