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Structure-activity relationship of orally potent tripeptide-based HIV protease inhibitors containing hydroxymethylcarbonyl isostere.
Mimoto T, Hattori N, Takaku H, Kisanuki S, Fukazawa T, Terashima K, Kato R, Nojima S, Misawa S, Ueno T, Imai J, Enomoto H, Tanaka S, Sakikawa H, Shintani M, Hayashi H, Kiso Y. Mimoto T, et al. Among authors: kisanuki s. Chem Pharm Bull (Tokyo). 2000 Sep;48(9):1310-26. doi: 10.1248/cpb.48.1310. Chem Pharm Bull (Tokyo). 2000. PMID: 10993230
[Anti-HIV compounds].
Kiso Y, Kisanuki S. Kiso Y, et al. Among authors: kisanuki s. Nihon Rinsho. 1993 Sep;51 Suppl:235-40. Nihon Rinsho. 1993. PMID: 8271390 Japanese. No abstract available.
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: kisanuki s. Chem Pharm Bull (Tokyo). 1991 Sep;39(9):2465-7. doi: 10.1248/cpb.39.2465. Chem Pharm Bull (Tokyo). 1991. PMID: 1804562