Author(s): Ballell L, Field RA, Chung GA, Young RJ
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Abstract The multiple parallel synthesis of a series of N,S-bis-alkylated thiopyrazolo[3,4-d]pyrimidines, based on sequential S- then N-alkylation, is reported. These compounds showed significant anti-mycobacterial activity (MICs down to 2mug/ml) and their potential as significant drug-like leads is substantiated through cytotoxicity evaluation and in silico profiling.
This article was published in Bioorg Med Chem Lett
and referenced in Medicinal Chemistry