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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.
Journal of Medicinal Chemistry|December 22, 2000
Synthesis of apicidin-derived quinolone derivatives: parasite-selective histone deacetylase inhibitors and antiproliferative agentsP T Meinke, S L Colletti, G Doss, et al.
Bioorganic & Medicinal Chemistry Letters|October 31, 2000
Chemical modification of nodulisporic acid A: preliminary structure-activity relationshipsP T Meinke, M B Ayer, S L Colletti, et al.
Bioorganic & Medicinal Chemistry Letters|September 15, 2000
Potent, selective 3-pyridylethanolamine beta3 adrenergic receptor agonists possessing a thiazole benzenesulfonamide pharmacophoreR J Mathvink, J S Tolman, D Chitty, 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 22, 2000
Human beta3-adrenergic receptor agonists containing 1,2,3-triazole-substituted benzenesulfonamidesL L Brockunier, E R Parmee, H O Ok, et al.
Bioorganic & Medicinal Chemistry Letters|August 18, 1999
Potent immunosuppressive C32-O-arylethyl ether derivatives of ascomycin with reduced toxicityH M Armstrong, F Wong, M A Holmes, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2001
Broad spectrum antiprotozoal agents that inhibit histone deacetylase: structure-activity relationships of apicidin. Part 2S L Colletti, R W Myers, S J Darkin-Rattray, et al.
Bioorganic & Medicinal Chemistry Letters|July 29, 2000
Substituted oxazole benzenesulfonamides as potent human beta3 adrenergic receptor agonistsH O Ok, L B Reigle, M R Candelore, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2001
Broad spectrum antiprotozoal agents that inhibit histone deacetylase: structure-activity relationships of apicidin. Part 1S L Colletti, R W Myers, S J Darkin-Rattray, et al.
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