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Description
Toxicity study CD-1 mice A 26-week Good Laboratory Practice (GLP) toxicology study was conducted at Inotiv according to the protocol, Inotivs Standard Operating Procedures and in compliance with the current US Food and Drug Administration GLP Regulations for Non-Clinical Studies (21 CFR Part 58)

Multiplexed thiol reactivity profiling for target discovery of electrophilic natural products

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Abandoned leads and replacement leads
