A Scaleable Synthesis of BAY 43-9006: A Potent Raf Kinase Inhibitor for the Treatment of Cancer
Author:
Affiliation:
1. Bayer Research Center, Pharmaceutical Division, 400 Morgan Lane, West Haven, Connecticut 06516, U.S.A.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/op020205n
Reference11 articles.
1. Serine- and threonine-specific protein kinase activities of purified gag–mil and gag–raf proteins
2. Antitumor activity of a phosphorothioate antisense oligodeoxynucleotide targeted against C-raf kinase
3. The discovery of potent cRaf1 kinase inhibitors
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