4-aryl quinols and analogs thereof as therapeutic agents

作者: Tracey Dawn Poole , Andrew David Westwell , Geoffrey Wells , Malcolm Francis Graham Stevens

DOI:

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摘要: The present invention pertains to compounds of the formula (1), which are, inter alia, antiproliferative agents, anticancer antimycobacterial antituberculosis and/or thioredoxin/thioredoxin reductase inhibitors: wherein: Q is =O or =N-S(=O)2-RQ;RQ -H optionally substituted C?1-7?alkyl, C3-20heterocyclyl, C5-20aryl; Ar R?o? an oxy substituent; bond marked α a single double bond; s R?3 and R5? are each independently ring substituents; R?2 R6? pharmaceutically acceptable salts, esters, amides, solvates, hydrates, protected forms thereof. also pharmaceutical compositions comprising such compounds, use compositions, both in vitro vivo, for example, treatment proliferative conditions, (e.g., cancer), mycobacterial infections tuberculosis), conditions mediated by reductase.

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