| Literature DB >> 14643307 |
Daisuke Shuto1, Soko Kasai, Tooru Kimura, Ping Liu, Koushi Hidaka, Takashi Hamada, Saeko Shibakawa, Yoshio Hayashi, Chinatsu Hattori, Beata Szabo, Shoichi Ishiura, Yoshiaki Kiso.
Abstract
A novel class of substrate-based beta-secretase (BACE1) inhibitors containing a hydroxymethylcarbonyl (HMC) isostere was designed and synthesized. Phenylnorstatine [(2R,3S)-3-amino-2-hydroxy-4-phenylbutyric acid; Pns] was an effective transition-state mimic at the P(1) position. Structure-activity relationships (SARs) of the P(3)-P(3)' positions of BACE1 inhibitors were studied.Entities:
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Year: 2003 PMID: 14643307 DOI: 10.1016/j.bmcl.2003.09.053
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823