| Literature DB >> 9784110 |
C M Tegley1, L Zhi, K B Marschke, M M Gottardis, Q Yang, T K Jones.
Abstract
A novel series of nonsteroidal progestins, 5-benzylidene-1, 2-dihydrochromeno[3,4-f]quinolines (2), was discovered, and a preliminary structure-activity relationship study around the 5-benzylidene ring generated several potent human progesterone receptor agonists (compounds 8, 16). These new progestins showed biological activities (EC50 = 5.7 and 7.6 nM) similar to progesterone (EC50 = 2.9 nM) in the cotransfection assay with high efficacy (132% and 166%) and binding affinity (Ki = 0.66 and 0.83 nM) similar to medroxyprogesterone acetate (MPA) (Ki = 0.34 nM). A representative analogue, 8, demonstrated similar oral potency to MPA in the uterine wet weight/mammary gland morphology assay in ovariectomized rats.Entities:
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Year: 1998 PMID: 9784110 DOI: 10.1021/jm980366a
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446