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- Journal Article
- A1
- open access
Expedient synthesis of lupulones and their derivatization to 2,8-7H-dihydrochromen-7-ones
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- Journal Article
- A1
- open access
Synthesis of indoline‐based benzhydroxamic acids as potential HDAC6 inhibitors
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Selective pharmacological inhibitors of HDAC6 reveal biochemical activity but functional tolerance in cancer models
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- PhD Thesis
- open access
Synthesis of selective HDAC6 inhibitors and their evaluation in cancer models
(2019) -
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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- Journal Article
- A1
- open access
Synthesis and anticancer properties of new (dihydro)pyranonaphthoquinones and their epoxy analogs
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- Journal Article
- A1
- open access
Expedient stereoselective synthesis of new dihydropyrano- and dihydrofuranonaphthoquinones