Discovery of heterocyclic ureas as a new class of raf kinase inhibitors: identification of a second generation lead by a combinatorial chemistry approach
- 1 October 2001
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 11 (20) , 2775-2778
- https://doi.org/10.1016/s0960-894x(01)00571-6
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Discovery of heterocyclic ureas as a new class of raf kinase inhibitors: identification of a second generation lead by a combinatorial chemistry approachBioorganic & Medicinal Chemistry Letters, 2001
- Protein kinase inhibitors: emerging pharmacophores 1997 - 2000Expert Opinion on Therapeutic Patents, 2001
- p38 Kinase inhibitors for the treatment of arthritis and osteoporosis: thienyl, furyl, and pyrrolyl ureasBioorganic & Medicinal Chemistry Letters, 2000
- Discovery of a new class of p38 kinase inhibitorsBioorganic & Medicinal Chemistry Letters, 2000
- 1-Phenyl-5-pyrazolyl ureas: potent and selective p38 kinase inhibitorsBioorganic & Medicinal Chemistry Letters, 2000
- Raf kinase inhibitorsExpert Opinion on Therapeutic Patents, 1998
- The Role of Raf Kinases in Development and Growth of TumorsPublished by Springer Nature ,1997
- Antitumor activity of a phosphorothioate antisense oligodeoxynucleotide targeted against C-raf kinaseNature Medicine, 1996
- Reconstitution of the Raf-1-MEK-ERK signal transduction pathway in vitro.Molecular and Cellular Biology, 1993
- FUNCTION AND REGULATION OF RASAnnual Review of Biochemistry, 1993