Design and synthesis of 7H-pyrrolo[2,3-d]pyrimidines as focal adhesion kinase inhibitors. Part 1.
Choi, Ha-Soon, Wang, Zhicheng, Richmond, Wendy, He, Xiaohui, Yang, Kunyong, Jiang, Tao, Sim, Taebo, Karanewsky, Donald, Gu, Xiang-Ju, Zhou, Vicki, Liu, Yi, Ohmori, Osamu, Caldwell, Jeremy, Gray, Nathanael and He, Yun (2006) Design and synthesis of 7H-pyrrolo[2,3-d]pyrimidines as focal adhesion kinase inhibitors. Part 1. Bioorganic & Medicinal Chemistry Letters, 16 (8). pp. 2173-2176. ISSN 0960-894X
Abstract
A series of 2-amino-9-aryl-7H-pyrrolo[2,3-d]pyrimidines were designed and synthesized to target focal adhesion kinase (FAK). A number of these pyrrolopyrimides exhibited low micromolar inhibitory activities against focal adhesion kinase, and their preliminary SAR was established via systematic chemical modifications. The 2-amino-9-aryl-7H-pyrrolo[2,3-d]pyrimidines represent a new class of kinase inhibitors.
Item Type: | Article |
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Additional Information: | author can archive post-print (ie final draft post-refereeing) |
Keywords: | Focal adhesion kinase; Inhibition; 7H-Pyrrolo[2,3-d]pyrimidines; SAR |
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Date Deposited: | 14 Dec 2009 14:04 |
Last Modified: | 31 Jan 2013 01:25 |
URI: | https://oak.novartis.com/id/eprint/164 |