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Bioorganic & Medicinal Chemistry Letters|September 25, 2002
Benzodiazepine inhibitors of the MMPs and TACEFrances C Nelson, Efren Delos Santos, Jeremy I Levin, et al.Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|February 24, 2001
[Migraine: dynamics of psychophysiologic pattern]A M Veĭn, A B Danilov, O A Kolosova, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 5, 2004
A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interactionJ Spampanato, J A Kearney, G de Haan, et al.Bioorganic & Medicinal Chemistry Letters|September 13, 2005
Synthesis and SAR of highly selective MMP-13 inhibitorsJianchang Li, Thomas S Rush, Wei Li, et al.Bioorganic & Medicinal Chemistry Letters|October 30, 2009
Non-hinge-binding pyrazolo[1,5-a]pyrimidines as potent B-Raf kinase inhibitorsDan M Berger, Nancy Torres, Minu Dutia, et al.Bioorganic & Medicinal Chemistry|October 12, 2005
Potent, selective, and orally bioavailable matrix metalloproteinase-13 inhibitors for the treatment of osteoarthritisYonghan Hu, Jason S Xiang, Martin J DiGrandi, et al.Bioorganic & Medicinal Chemistry Letters|April 6, 2002
Anthranilate sulfonamide hydroxamate TACE inhibitors. Part 2: SAR of the acetylenic P1' groupJ I Levin, J M Chen, M T Du, et al.Bioorganic & Medicinal Chemistry Letters|March 23, 2011
Design and SAR of macrocyclic Hsp90 inhibitors with increased metabolic stability and potent cell-proliferation activityChristoph W Zapf, Jonathan D Bloom, Jamie L McBean, et al.Bioorganic & Medicinal Chemistry Letters|February 24, 2001
Heteroaryl and cycloalkyl sulfonamide hydroxamic acid inhibitors of matrix metalloproteinasesJ I Levin, Y Gu, F C Nelson, et al.Bioorganic & Medicinal Chemistry Letters|October 31, 2009
Novel pyrazolopyrimidines as highly potent B-Raf inhibitorsMartin J Di Grandi, Dan M Berger, Darrin W Hopper, et al.Pageof 30