A novel strategy for designing irreversible inhibitors of metalloproteases: Acetals as latent electrophiles that interact with catalytic nucleophile at the active site

Citation
Ms. Han et al., A novel strategy for designing irreversible inhibitors of metalloproteases: Acetals as latent electrophiles that interact with catalytic nucleophile at the active site, ORG LETT, 2(20), 2000, pp. 3149-3152
Citations number
24
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
2
Issue
20
Year of publication
2000
Pages
3149 - 3152
Database
ISI
SICI code
1523-7060(20001005)2:20<3149:ANSFDI>2.0.ZU;2-Q
Abstract
[GRAPHICS] A new strategy for design of irreversible inactivators for carboxypeptidase A (CPA), a prototypic zinc protease, has been developed by exploiting the property of acetals to generate an oxacarbenium ion intermediate in the con version into the corresponding carbonyl compounds. The design strategy is e xemplified by 2-benzyl 5-alkyl-3,5 dioxapentanoic acids (la-c), Interesting ly, (R) lb is slightly more potent than an (S)-1b as an inactivator of CPA.