Synthesis and evaluation of isatin analogs as caspase-3 inhibitors: Introduction of a hydrophilic group increases potency in a whole cell assay
In: Bioorganic & medicinal chemistry letters (Print), Jg. 21 (2011), Heft 8, S. 2192-2197
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Zugriff:
A series of isatin analogs containing a hydrophilic group, including a pyridine ring, ethylene glycol group, and a triazole ring, have been synthesized, and their inhibition potency for caspase-3 was measured both in vitro (i.e., recombinant enzyme) and in whole cells (HeLa cells). The analogs having a hydrophilic group, including 12, 13, 16, 38, and 40, have dramatically increased activity in vitro and in HeLa cells compared to the corresponding unsubstituted N-phenyl isatin analogs.
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Synthesis and evaluation of isatin analogs as caspase-3 inhibitors: Introduction of a hydrophilic group increases potency in a whole cell assay
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Autor/in / Beteiligte Person: | WENHUA, CHU ; ROTHFUSS, Justin ; DONG, ZHOU ; MACH, Robert H |
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Zeitschrift: | Bioorganic & medicinal chemistry letters (Print), Jg. 21 (2011), Heft 8, S. 2192-2197 |
Veröffentlichung: | Amsterdam: Elsevier, 2011 |
Medientyp: | academicJournal |
Umfang: | print, |
ISSN: | 0960-894X (print) |
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