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2000
Volume 16, Issue 4
  • ISSN: 1568-0266
  • E-ISSN: 1873-4294

Abstract

Metalloproteins have attracted momentous attentions for the treatment of many human diseases, including cancer, HIV, hypertension, etc. This article reviews the progresses that have been made in the field of drug development of metalloprotein inhibitors, putting emphasis on the targets of carbonic anhydrase, histone deacetylase, angiotensin converting enzyme, and HIV-1 integrase. Many other important metalloproteins are also briefly discussed. The binding and coordination modes of different marketed metalloprotein inhibitors are stated, providing insights to design novel metal binding groups and further novel inhibitors for metalloproteins.

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/content/journals/ctmc/10.2174/1568026615666150813145218
2016-02-01
2025-01-13
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  • Article Type:
    Research Article
Keyword(s): Chelating; Drug design; Drug development; Magnesium; Metalloprotein; Zinc
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