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Identification of Better Pharmacokinetic Benzothiazinone Derivatives as New Antitubercular Agents.

ABSTRACT: A series of new 8-nitro-6-(trifluoromethyl)-1,3-benzothiazin-4-one(BTZ) derivatives containing a C-2 nitrogen spiro-heterocycle moiety based on the structures of BTZ candidates BTZ043 and PBTZ169 were designed and synthesized as new antitubercular agents. Many of them were found to have excellent in vitro activity (MIC < 0.15 ?M) against the drug susceptive Mycobacterium tuberculosis H37Rv strain and two clinically isolated multidrug-resistant strains. Compounds 11l and 11m display acceptable safety, greater aqueous solubility, and better pharmacokinetic profiles than PBTZ169, suggesting their promising potential to be lead compounds for future antitubercular drug discovery.

SUBMITTER: Lv K

PROVIDER: S-EPMC5467196 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

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Identification of Better Pharmacokinetic Benzothiazinone Derivatives as New Antitubercular Agents.

Lv Kai K You Xuefu X Wang Bin B Wei Zengquan Z Chai Yun Y Wang Bo B Wang Apeng A Huang Guocheng G Liu Mingliang M Lu Yu Y

ACS medicinal chemistry letters 20170510 6

A series of new 8-nitro-6-(trifluoromethyl)-1,3-benzothiazin-4-one(BTZ) derivatives containing a C-2 nitrogen spiro-heterocycle moiety based on the structures of BTZ candidates BTZ043 and PBTZ169 were designed and synthesized as new antitubercular agents. Many of them were found to have excellent in vitro activity (MIC < 0.15 μM) against the drug susceptive Mycobacterium tuberculosis H37Rv strain and two clinically isolated multidrug-resistant strains. Compounds 11l and 1 ...[more]

PMID: 28626525

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