Novel isoxazole thiophene-containing compounds active against Mycobacterium tuberculosis

Screening of the ChemDiv molecular library in cholesterol media against Mycobacterium tuberculosis (Mtb) H37Rv strain identified a novel isoxazole thiophene hit as a putative Rv1625c/Cya activator with a promising in vitro activity and good pharmacokinetic properties. Twenty-nine analogs were synthesized to assess the structure-activity relationships (SAR) to further improve potency. The most notable analog was P15, which showed an intramacrophage EC<sub>50</sub> = 1.96 µM and exhibited 58.0 % oral bioavailability when it was dosed orally at 20 mg/kg in a mouse pharmacokinetic (PK) study. The overall medicinal chemistry campaign revealed limited SAR that did not support further investigation into this series.

Authors

Institutions

Publication Details

Journal
Bioorganic & Medicinal Chemistry Letters
Published
2025-01-23
DOI
https://doi.org/10.1016/j.bmcl.2025.130108
Citations
5
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
6.98

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Novel isoxazole thiophene-containing compounds active against Mycobacterium tuberculosis

Paridhi Sukheja, J. C. Webb, Case W. McNamara, Arnab K. Chatterjee et al.
5 citations
Bioorganic & Medicinal Chemistry Letters
Tuberculosis Research and Epidemiology
6.98
article

Novel isoxazole thiophene-containing compounds active against Mycobacterium tuberculosis

Paridhi Sukheja, J. C. Webb, Case W. McNamara, Arnab K. Chatterjee, Baiyuan Yang, G. M. Martínez, Kirsten Tolentino
article en
5 citations

Abstract

Screening of the ChemDiv molecular library in cholesterol media against Mycobacterium tuberculosis (Mtb) H37Rv strain identified a novel isoxazole thiophene hit as a putative Rv1625c/Cya activator with a promising in vitro activity and good pharmacokinetic properties. Twenty-nine analogs were synthesized to assess the structure-activity relationships (SAR) to further improve potency. The most notable analog was P15, which showed an intramacrophage EC<sub>50</sub> = 1.96 µM and exhibited 58.0 % oral bioavailability when it was dosed orally at 20 mg/kg in a mouse pharmacokinetic (PK) study. The overall medicinal chemistry campaign revealed limited SAR that did not support further investigation into this series.

Bioorganic & Medicinal Chemistry LettersVol. 119
Scripps Research Institute (US)
Bill and Melinda Gates Foundation
Good health and well-being
Openalex Percentile: Top 4%
Tuberculosis Research and Epidemiology
6.98
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.