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Synthesis and cancer cell cytotoxicity of 6-, 7-, or 8-substituted 2-(hetero)aryl-4-(4-(hetero)aryl-2-oxobut-3-en-1-ylidene)benzothiazepanes
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Synthesis and functional screening of novel inhibitors targeting the HDAC6 zinc finger ubiquitin-binding domain
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- Journal Article
- A1
- open access
Synthesis and cancer cell cytotoxicity of 2-heteroaryl-4-(4-heteroaryl-2-oxobut-3-en-1-ylidene)-substituted benzothiazepanes
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Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents
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Synthesis and anticancer activity assessment of curcumin-inspired benzothiazepane derivatives
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- Journal Article
- A1
- open access
Synthesis and cancer cell cytotoxicity of 2-aryl-4-(4-aryl-2-oxobut-3-en-1-ylidene)-substituted benzothiazepanes
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Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents
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Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents
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The natural product curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents
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The natural product curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents