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对结核分枝杆菌具有活性的新型含异恶唑噻吩化合物。

Novel isoxazole thiophene-containing compounds active against Mycobacterium tuberculosis.

作者信息

Martinez Gabrielle, Tolentino Kirsten, Sukheja Paridhi, Webb Jasmine, McNamara Case W, Chatterjee Arnab K, Yang Baiyuan

机构信息

Calibr-Skaggs Institute for Innovative Medicines, a division of Scripps Research, La Jolla, CA 92037, United States.

Calibr-Skaggs Institute for Innovative Medicines, a division of Scripps Research, La Jolla, CA 92037, United States.

出版信息

Bioorg Med Chem Lett. 2025 Apr 15;119:130108. doi: 10.1016/j.bmcl.2025.130108. Epub 2025 Jan 23.

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 = 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.

摘要

在胆固醇培养基中对ChemDiv分子文库进行针对结核分枝杆菌(Mtb)H37Rv菌株的筛选,鉴定出一种新型异恶唑噻吩命中物,作为假定的Rv1625c/Cya激活剂,具有良好的体外活性和药代动力学性质。合成了29种类似物以评估构效关系(SAR),以进一步提高效力。最显著的类似物是P15,在小鼠药代动力学(PK)研究中,当以20mg/kg口服给药时,其巨噬细胞内EC = 1.96µM,口服生物利用度为58.0%。整个药物化学研究表明,构效关系有限,不支持对该系列进行进一步研究。

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