Reinvestigation of the structure-activity relationships of isoniazid

Pooja Hegde, Helena I.M. Boshoff, Yudi Rusman, Wassihun Wedajo Aragaw, Christine E. Salomon, Thomas Dick, Courtney C. Aldrich

Research output: Contribution to journalArticlepeer-review

Abstract

Isoniazid (INH) remains a cornerstone for treatment of drug susceptible tuberculosis (TB), yet the quantitative structure-activity relationships for INH are not well documented in the literature. In this paper, we have evaluated a systematic series of INH analogs against contemporary Mycobacterium tuberculosis strains from different lineages and a few non-tuberculous mycobacteria (NTM). Deletion of the pyridyl nitrogen atom, isomerization of the pyridine nitrogen to other positions, replacement of the pyridine ring with isosteric heterocycles, and modification of the hydrazide moiety of INH abolishes antitubercular activity. Similarly, substitution of the pyridine ring at the 3-position is not tolerated while substitution at the 2-position is permitted with 2-methyl-INH 9 displaying antimycobacterial activity comparable to INH. To assess the specific activity of this series of INH analogs against mycobacteria, we assayed them against a panel of gram-positive and gram-negative bacteria, as well as a few fungi. As expected INH and its analogs display a narrow spectrum of activity and are inactive against all non-mycobacterial strains evaluated, except for 4, which has modest inhibitory activity against Cryptococcus neoformans. Our findings provide an updated analysis of the structure-activity relationship of INH that we hope will serve as useful resource for the community.

Original languageEnglish (US)
Article number102100
JournalTuberculosis
Volume129
DOIs
StatePublished - Jul 1 2021

Bibliographical note

Funding Information:
This work was supported by grants ( AI136445 and AI143784 ) from the National Institutes of Health and in part by the Intramural Research Program of NIAID ( AI000693 ). The NMR facility used for the characterization of compounds was supported in part by a NIH S10 instrumentation grant OD021536 (G. Veglia).

Publisher Copyright:
© 2021 Elsevier Ltd

Keywords

  • Isoniazid
  • SAR

PubMed: MeSH publication types

  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

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