Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10591978 | Bioorganic & Medicinal Chemistry Letters | 2013 | 5 Pages |
Abstract
Tricyclic thiazoleamine derivatives that were identified as hits in a screen against human umbilical vein endothelial cell proliferation were subjected to a structure-activity relationship study. Two structurally superimposable scaffolds-4H-thiochromeno[4,3-d]thiazol-2-amine and 5,6-dihydro-4H-benzo[6,7]cyclohepta[1,2-d]thiazol-2-amine derivatives-yielded low-micromolar inhibitors, and two among them 37 and 43 also exhibited antiangiogenic activity in an endothelial tube formation assay. Thus, 37 and 43 can serve as leads to develop a novel class of antiangiogenic agents.
Keywords
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shridhar Bhat, Joong Sup Shim, Jun O. Liu,