DprE1 Inhibitors: Enduring Aspirations for Future Antituberculosis Drug Discovery

Saloni Yadav, Aastha Soni, Omprakash Tanwar, Rajendra Bhadane, Gurdyal S Besra, Neha Kawathekar

Research output: Contribution to journalReview Article or Literature Reviewpeer-review

6 Citations (Scopus)
21 Downloads (Pure)

Abstract

DprE1 is a crucial enzyme involved in the cell wall synthesis of Mycobacterium tuberculosis and a promising target for antituberculosis drug development. However, its unique structural characteristics for ligand binding and association with DprE2 make developing new clinical compounds challenging. This review provides an in-depth analysis of the structural requirements for both covalent and non-covalent inhibitors, their 2D and 3D binding patterns, as well as their biological activity data in vitro and in vivo, including pharmacokinetic information. We also introduce a protein quality score (PQS) and an active-site map of the DprE1 enzyme to help medicinal chemists better understand DprE1 inhibition and develop new and effective anti-TB drugs. Furthermore, we examine the resistance mechanisms associated with DprE1 inhibitors to understand future developments due to resistance emergence. This comprehensive review offers insight into the DprE1 active site, including protein-binding maps, PQS, and graphical representations of known inhibitors, making it a valuable resource for medicinal chemists working on future antitubercular compounds.

Original languageEnglish
Article numbere202300099
Number of pages31
JournalChemMedChem
Volume18
Issue number16
DOIs
Publication statusPublished - 15 Aug 2023
MoE publication typeA2 Review article in a scientific journal

Keywords

  • DprE1
  • Mycobacterium tuberculosis
  • DprE2

Fingerprint

Dive into the research topics of 'DprE1 Inhibitors: Enduring Aspirations for Future Antituberculosis Drug Discovery'. Together they form a unique fingerprint.

Cite this