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Discovery of 4-Aryl-4H-chromenes as a New Series of Apoptosis Inducers Using a Cell- and Caspase-Based Hight-Throughput Screening Assay. Part 2. Structure—Activity Relationships of the 7- and 5-, 6-, 8-Positions.

✍ Scribed by Sui Xiong Cai; et al. et al.


Publisher
John Wiley and Sons
Year
2006
Weight
14 KB
Volume
37
Category
Article
ISSN
0931-7597

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✦ Synopsis


Medicinal chemistry V 1100 Discovery of 4-Aryl-4H-chromenes as a New Series of Apoptosis Inducers Using a Cell-and Caspase-Based Hight-Throughput Screening Assay. Part 2. Structure-Activity Relationships of the 7-and 5-, 6-, 8-Positions. -The structure-activity relationships of novel derivatives such as (I) are discussed. Small hydrophobic groups at the 7-position are preferred and disubstitution at 7,8-position, cf. derivatives (Ic) and (Id), results in potent compounds. -(CAI*, S. X.; et al.; Bioorg.