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Bioorganic & Medicinal Chemistry Letters|June 27, 2001
Potent nonpeptide GnRH receptor antagonists derived from substituted indole-5-carboxamides and -acetamides bearing a pyridine side-chain terminusW T Ashton, R M Sisco, Y T Yang, et al.Bioorganic & Medicinal Chemistry Letters|August 11, 2000
Quinolones as gonadotropin releasing hormone (GnRH) antagonists: simultaneous optimization of the C(3)-aryl and C(6)-substituentsJ R Young, S X Huang, I Chen, et al.Bioorganic & Medicinal Chemistry Letters|April 1, 2000
Potent antagonists of gonadotropin releasing hormone receptors derived from quinolone-6-carboxamidesT F Walsh, R B Toupence, J R Young, et al.Bioorganic & Medicinal Chemistry Letters|September 12, 2001
Orally bioavailable, indole-based nonpeptide GnRH receptor antagonists with high potency and functional activityW T Ashton, R M Sisco, G R Kieczykowski, et al.Journal of Medicinal Chemistry|April 13, 2001
A potent, nonpeptidyl 1H-quinolone antagonist for the gonadotropin-releasing hormone receptorR J DeVita, T F Walsh, J R Young, et al.Pageof 2