Design and Synthesis of 5,6-fused Heterocyclic Amides as Raf Kinase Inhibitors
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Ramurthy, Savithri, Costales, Abran, Aikawa, Mina, Amiri, Payman, Jansen, Johanna, Lin, Song, Ma, Sylvia, Renhowe, Paul, Shafer, Cynthia, Subramanian, Sharadha, Sung, L and Verhagen, J (2011) Design and Synthesis of 5,6-fused Heterocyclic Amides as Raf Kinase Inhibitors. Bioorganic Medicinal Chemistry Letters, 21 (11). pp. 3286-3289. ISSN 0960-894X
Official URL: http://www.sciencedirect.com/science/journal/09608...
Abstract
Two novel scaffolds based on 5,6-fused heterocyclic backbones were designed and synthesized as Raf kinase inhibitors. The scaffolds were assessed for in vitro pan-Raf inhibition, activity in cell proliferation and target modulation assays, and pharmacokinetic parameters.
Item Type: | Article |
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Additional Information: | author can archive post-print (ie final draft post-refereeing); Publisher's version/PDF cannot be used |
Keywords: | Benzoxazoles, benzothiazoles, raf inhibitors |
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Date Deposited: | 13 Oct 2015 13:15 |
Last Modified: | 13 Oct 2015 13:15 |
URI: | https://oak.novartis.com/id/eprint/4316 |