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Bioorganic & Medicinal Chemistry Letters|January 5, 1999
5-Alkyl 1,2-dihydrochromeno[3,4-f]quinolines: a novel class of nonsteroidal progesterone receptor modulatorsL Zhi, C M Tegley, J P Edwards, et al.Journal of Medicinal Chemistry|March 4, 1998
Synthesis and biological activity of a novel series of nonsteroidal, peripherally selective androgen receptor antagonists derived from 1,2-dihydropyridono[5,6-g]quinolinesL G Hamann, R I Higuchi, L Zhi, et al.Journal of Medicinal Chemistry|July 21, 1998
Preparation, resolution, and biological evaluation of 5-aryl-1, 2-dihydro-5H-chromeno[3,4-f]quinolines: potent, orally active, nonsteroidal progesterone receptor agonistsJ P Edwards, L Zhi, C L Pooley, et al.Bioorganic & Medicinal Chemistry Letters|May 7, 1999
Nonsteroidal androgen receptor agonists based on 4-(trifluoromethyl)-2H-pyrano[3,2-g]quinolin-2-oneJ P Edwards, R I Higuchi, D T Winn, et al.Nature|December 12, 1991
Human immunodeficiency virus genetic variation that can escape cytotoxic T cell recognitionR E Phillips, S Rowland-Jones, D F Nixon, et al.Bioorganic & Medicinal Chemistry Letters|May 26, 1999
4-Alkyl- and 3,4-dialkyl-1,2,3,4-tetrahydro-8-pyridono[5,6-g]quinolines: potent, nonsteroidal androgen receptor agonistsR I Higuchi, J P Edwards, T R Caferro, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Nonsteroidal progesterone receptor antagonists based on a conformationally-restricted subseries of 6-aryl-1,2-dihydro-2,2,4-trimethylquinolinesL G Hamann, D T Winn, C L Pooley, et al.Pageof 10