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Structure-activity relationship of orally potent tripeptide-based HIV protease inhibitors containing hydroxymethylcarbonyl isostere.
Chem Pharm Bull (Tokyo). 2000 Sep;48(9):1310-26. doi: 10.1248/cpb.48.1310.
Chem Pharm Bull (Tokyo). 2000.
PMID: 10993230
Rational design and synthesis of a novel class of active site-targeted HIV protease inhibitors containing a hydroxymethylcarbonyl isostere. Use of phenylnorstatine or allophenylnorstatine as a transition-state mimic.
Mimoto T, Imai J, Tanaka S, Hattori N, Takahashi O, Kisanuki S, Nagano Y, Shintani M, Hayashi H, Sakikawa H, et al.
Mimoto T, et al. Among authors: sakikawa h.
Chem Pharm Bull (Tokyo). 1991 Sep;39(9):2465-7. doi: 10.1248/cpb.39.2465.
Chem Pharm Bull (Tokyo). 1991.
PMID: 1804562
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