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 (K-i = 0.66 and 0.83 nM) similar to medroxyprogesterone acetate (MPA) (K-i = 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.Chemistry, MedicinalSCI(E)16ARTI...
Alkylated derivatives of 17-acetoxyprogesterone were prepared in order to test the hypothesis that b...
The synthesis, binding affinity for estrogen receptor subtypes (ER alpha and ER beta) and pharmacolo...
Antigestagens (antiprogestins) are functional competitors of progesterone (P4) that prevent P4 from ...
The progesterone receptor (PR) plays an important role in various physiological systems, including f...
Considering the significance of progesterone receptor (PR) modulators, the present study is explored...
The pharmacological properties of progestins used in contraception and hormone replacement therapy (...
In early pregnancy, abortion can be induced by blocking the actions of progesterone receptors (PR). ...
International audienceThe human pregnane X receptor (hPXR) is a nuclear receptor that regulates the ...
Hormones are vital molecules for human differentiation, development, and health. Among them, the fem...
International audienceThe human pregnane X receptor (hPXR) is a nuclear receptor that regulates the ...
International audienceThe human pregnane X receptor (hPXR) is a nuclear receptor that regulates the ...
234 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1994.Chemical probes for steroid r...
The synthetic progestins used so far for contraception and menopausal hormone therapy are derived ei...
Contains fulltext : 92379.pdf (publisher's version ) (Open Access)8 p
The progesterone receptor (PR) is an important member of the nuclear receptor superfamily of transcr...
Alkylated derivatives of 17-acetoxyprogesterone were prepared in order to test the hypothesis that b...
The synthesis, binding affinity for estrogen receptor subtypes (ER alpha and ER beta) and pharmacolo...
Antigestagens (antiprogestins) are functional competitors of progesterone (P4) that prevent P4 from ...
The progesterone receptor (PR) plays an important role in various physiological systems, including f...
Considering the significance of progesterone receptor (PR) modulators, the present study is explored...
The pharmacological properties of progestins used in contraception and hormone replacement therapy (...
In early pregnancy, abortion can be induced by blocking the actions of progesterone receptors (PR). ...
International audienceThe human pregnane X receptor (hPXR) is a nuclear receptor that regulates the ...
Hormones are vital molecules for human differentiation, development, and health. Among them, the fem...
International audienceThe human pregnane X receptor (hPXR) is a nuclear receptor that regulates the ...
International audienceThe human pregnane X receptor (hPXR) is a nuclear receptor that regulates the ...
234 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1994.Chemical probes for steroid r...
The synthetic progestins used so far for contraception and menopausal hormone therapy are derived ei...
Contains fulltext : 92379.pdf (publisher's version ) (Open Access)8 p
The progesterone receptor (PR) is an important member of the nuclear receptor superfamily of transcr...
Alkylated derivatives of 17-acetoxyprogesterone were prepared in order to test the hypothesis that b...
The synthesis, binding affinity for estrogen receptor subtypes (ER alpha and ER beta) and pharmacolo...
Antigestagens (antiprogestins) are functional competitors of progesterone (P4) that prevent P4 from ...