| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1365180 | Bioorganic & Medicinal Chemistry Letters | 2008 | 5 Pages |
Abstract
The synthesis and structure–activity relationships (SAR) of Chk1 inhibitors based on a 5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one core are described. Specifically, an exploration of the 7 and 8 positions on this previously disclosed core afforded compounds with improved enzymatic and cellular potency.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Investigation of novel 7,8-disubstituted-5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-ones as potent Chk1 inhibitors](/preview/png/1365180.png "First Page Preview: Investigation of novel 7,8-disubstituted-5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-ones as potent Chk1 inhibitors")
Authors
Lisa A. Hasvold, Le Wang, Magdalena Przytulinska, Zhan Xiao, Zehan Chen, Wen-Zhen Gu, Philip J. Merta, John Xue, Peter Kovar, Haiying Zhang, Chang Park, Thomas J. Sowin, Saul H. Rosenberg, Nan-Horng Lin,