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Aspartyl alpha-((diphenylphosphinyl)oxy)methyl ketones as novel inhibitors of interleukin-1 beta converting enzyme. Utility of the diphenylphosphinic acid leaving group for the inhibition of cysteine proteases.
Dolle RE, Singh J, Whipple D, Osifo IK, Speier G, Graybill TL, Gregory JS, Harris AL, Helaszek CT, Miller RE, et al. Dolle RE, et al. Among authors: miller re. J Med Chem. 1995 Jan 20;38(2):220-2. doi: 10.1021/jm00002a002. J Med Chem. 1995. PMID: 7830263 No abstract available.
Aspartyl alpha-((1-phenyl-3-(trifluoromethyl)-pyrazol-5-yl)oxy)methyl ketones as interleukin-1 beta converting enzyme inhibitors. Significance of the P1 and P3 amido nitrogens for enzyme-peptide inhibitor binding.
Dolle RE, Singh J, Rinker J, Hoyer D, Prasad CV, Graybill TL, Salvino JM, Helaszek CT, Miller RE, Ator MA. Dolle RE, et al. Among authors: miller re. J Med Chem. 1994 Nov 11;37(23):3863-6. doi: 10.1021/jm00049a001. J Med Chem. 1994. PMID: 7966144 No abstract available.
In vitro antimalarial activity of chalcones and their derivatives.
Li R, Kenyon GL, Cohen FE, Chen X, Gong B, Dominguez JN, Davidson E, Kurzban G, Miller RE, Nuzum EO, et al. Li R, et al. Among authors: miller re. J Med Chem. 1995 Dec 22;38(26):5031-7. doi: 10.1021/jm00026a010. J Med Chem. 1995. PMID: 8544179
718 results