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Nitrofuranyl Methyl Piperazines as New Anti-TB Agents: Identification, Validation, Medicinal Chemistry, and PK Studies

2015; American Chemical Society; Volume: 6; Issue: 10 Linguagem: Inglês

10.1021/acsmedchemlett.5b00141

1948-5875

Kushalava Reddy Yempalla, Gurunadham Munagala, Samsher Singh, Asmita Magotra, Sunil Kumar, Vikrant Singh Rajput, Sonali S. Bharate, Manoj Tikoo, Gurdarshan Singh, Inshad Ali Khan, Ram A. Vishwakarma, Parvinder Pal Singh,

Cancer therapeutics and mechanisms

Whole-cell screening of 20,000 drug-like small molecules led to the identification of nitrofuranyl methylpiperazines as potent anti-TB agents. In the present study, validation followed by medicinal chemistry has been used to explore the structure-activity relationship. Ten compounds demonstrated potent MIC in the range of 0.17-0.0072 μM against H37Rv Mycobacterium tuberculosis (MTB) and were further investigated against nonreplicating and resistant (Rif(R) and MDR) strains of MTB. These compounds were also tested for cytotoxicity. Among the 10 tested compounds, five showed submicromolar to nanomolar potency against nonreplicating and resistant (Rif(R) and MDR) strains of MTB along with a good safety index. Based on their overall in vitro profiles, the solubility and pharmacokinetic properties of five potent compounds were studied, and two analogues, 14f and 16g, were found to have comparatively better solubility than others tested and acceptable pharmacokinetic properties. This study presents the rediscovery of a nitrofuranyl class of compounds with improved aqueous solubility and acceptable oral PK properties, opening a new direction for further development.