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• W2054592578 abstract "The development of a novel class of nonsteroidal human progesterone receptor (hPR) agonists, 5-aryl-1,2-dihydro-5H-chromeno[3,4-f]quinolines 2, is described. The introduction of a 5-aryl group into the 1,2-dihydrocoumarino[3,4-f]quinoline core 1 is the key for progestational activities. The structure−activity relationship (SAR) studies of the 5-aryl substituents generated a series of potent hPR agonists, which exhibited similar biological activity (EC50 = 8−30 nM) to the natural hormone progesterone (EC50 = 2.9 nM) in cell-based assays with efficacies ranging from 28% to 96%. Most of the analogues displayed similar or greater binding affinity (Ki = 0.41−3.6 nM) than progesterone (Ki = 3.5 nM). Three representative analogues (13, 15, and 24) demonstrated in vivo activities in mammary gland morphology/uterine wet weight assay in ovariectomized rats." @default.
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• W2054592578 date "1998-01-01" @default.
• W2054592578 modified "2023-09-27" @default.
• W2054592578 title "5-Aryl-1,2-dihydrochromeno[3,4-<i>f</i>]quinolines: A Novel Class of Nonsteroidal Human Progesterone Receptor Agonists" @default.
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• W2054592578 doi "https://doi.org/10.1021/jm9705768" @default.
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