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rdf:type |
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|
lifeskim:mentions |
|
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pubmed:issue |
6
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pubmed:dateCreated |
1999-1-26
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pubmed:abstractText |
Design and synthesis of a series of very potent nonpeptide HIV protease inhibitors are described. The inhibitors are derived from novel high affinity P2-ligands and (R)-(hydroxyethylamino)sulfonamide isostere.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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|
pubmed:citationSubset |
IM
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|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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pubmed:month |
Mar
|
|
pubmed:issn |
0960-894X
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|
pubmed:author |
pubmed-author:ButhodJJ,
pubmed-author:ChoHH,
pubmed-author:ChuMM,
pubmed-author:GhoshA KAK,
pubmed-author:HollandLL,
pubmed-author:HussainK AKA,
pubmed-author:KincaidJ FJF,
pubmed-author:KouCC,
pubmed-author:KrishnanKK,
pubmed-author:RudallCC,
pubmed-author:WaltersD EDE
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|
pubmed:issnType |
Print
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|
pubmed:day |
17
|
|
pubmed:volume |
8
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
687-90
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
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pubmed:year |
1998
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|
pubmed:articleTitle |
Potent HIV protease inhibitors incorporating high-affinity P2-ligands and (R)-(hydroxyethylamino)sulfonamide isostere.
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|
pubmed:affiliation |
Department of Chemistry, University of Illinois at Chicago 60607, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|
