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3H-1,2,4-Dithiazol-3-one Compounds as Novel Potential Affordable Antitubercular Agents

3H-1,2,4-Dithiazol-3-one Compounds as Novel Potential Affordable Antitubercular Agents

Jianzhong Yang, Weiyi Pi, Li Xiong, Wei Ang, Tao Yang, Jun He, Yuanyuan Liu, Ying Chang, Weiwei Ye, Zhenling Wang, Youfu Luo, Yuquan Wei

Bioorg Med Chem Lett. 2013 Mar 1;23(5):1424-7.

PMID: 23337602

Abstract:

Small molecules with oxathiazol-2-one moiety were recently reported as potent inhibitors of Mycobacterium bovis var. bacilli Calmette-Guérin (BCG), among which HT1171 was the most potent and selective proteasome inhibitor. Herein we synthesized a series of novel compounds by bioisosteric replacement of the oxathiazol-2-one ring with 3H-1,2,4-dithiazol-3-one, and also fifteen 1,3,4-oxathiazol-2-one molecules in order for potency comparison and structure-activity relationship elucidation since their antibacterial effects on the virulent strains were not evaluated before. All the compounds were assessed for antitubercular activities on the virulent H37Rv strain by a serial dilution method. Among the tested compounds, 3H-1,2,4-dithiazol-3-one compound 4n was found to be the most active with a lowest MIC(90) value of 1 μg/mL. Furthermore, the cytotoxicities of all the compounds against normal human liver cell line L02 were determined by an MTT method. Compound 4n displayed a lower inhibitory ratio than HT1171 at the concentration of 100 μM, indicating its better safety profile.

Chemicals Related in the Paper:

Catalog Number	Product Name	Structure	CAS Number	Price
AP192880969	HT1171		192880-96-9	Price

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