Non-classical β-carbonic anhydrase inhibitors-towards novel anti-mycobacterials
Author(s) -
Natascha von Gnielinski,
Lisa Nienaber,
Lyndel Mason,
Samantha Ellis,
James A. Triccas,
Rohan A. Davis,
Andreas Hofmann
Publication year - 2014
Publication title -
medchemcomm
Language(s) - English
Resource type - Journals
eISSN - 2040-2511
pISSN - 2040-2503
DOI - 10.1039/c4md00310a
Subject(s) - carbonic anhydrase , carbonic anhydrase ii , chemistry , computational biology , biochemistry , enzyme , biology
Mycobacterial carbonic anhydrases, such as the essential protein Rv3588c, are attractive drug targets since they constitute a different class of carbonic anhydrases than those found in humans. A natural product library has been screened for compounds that inhibit mycobacterial carbonic anhydrases but lack the much-exploited sulfonamide/sulfamate group. The identified inhibitors of mycobacterial Rv3588c are likely to affect the enzyme at a site different from the catalytic centre - a concept which may be exploited for novel specific anti-mycobacterials.Griffith Sciences, Griffith Institute for Drug DiscoveryFull Tex
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