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2000
Volume 5, Issue 4
  • ISSN: 1389-5575
  • E-ISSN: 1875-5607

Abstract

1,2,4-Thiadiazole is a distinctive class of small heterocyclic thiol trapping agents that serve as an interesting pharmacophore in the design of inhibitors targeting the cysteine residues of proteins. X-Ray crystal structures of enzyme-inhibitor complex indicate that the cysteine thiol reacts with the N-S bond of the thiadiazole moiety to form a disulfide bond resulting in the inactivation of the enzymes. This review addresses the medicinal chemistry and various properties of 1,2,4-thiadiazoles in their potential as new electrophilic “warheads” for targeting the cysteine residues of biomolecules (e.g, H+ / K+ ATPase), and cysteine-dependent enzymes (e.g., cathepsin B and transglutaminase).

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/content/journals/mrmc/10.2174/1389557053544056
2005-04-01
2025-09-05
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/content/journals/mrmc/10.2174/1389557053544056
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