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Assessment of the trifluoromethyl ketone functionality as an alternative zinc-binding group for selective HDAC6 inhibition
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- Journal Article
- A1
- open access
Synthesis of potent and selective HDAC6 inhibitors bearing a cyclohexane- or cycloheptane-annulated 1,5-benzothiazepine scaffold
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- Journal Article
- A1
- open access
Synthesis and SAR assessment of novel Tubathian analogs in the pursuit of potent and selective HDAC6 inhibitors
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Synthesis of benzothiophene-based hydroxamic acids as potent and selective HDAC6 inhibitors