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Discovery of 6-N,N-Bis(2,2,2-trifluoroethyl)amino- 4-trifluoromethylquinolin-2(1H)-one as a Novel Selective Androgen Receptor Modulator

Journal of medicinal chemistry, 2006-10, Vol.49 (21), p.6143-6146

2006

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Meclizine Is an Agonist Ligand for Mouse Constitutive Androstane Receptor (CAR) and an Inverse Agonist for Human CAR

Molecular endocrinology (Baltimore, Md.), 2004-10, Vol.18 (10), p.2402-2408

2004

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Synthesis and biological activity of 5-methylidene 1,2-dihydrochromeno[3,4- f]quinoline derivatives as progesterone receptor modulators

Bioorganic & medicinal chemistry letters, 2003-06, Vol.13 (12), p.2071-2074

2003

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Androgen Receptor-Mediated Apoptosis Is Regulated by Photoactivatable Androgen Receptor Ligands

Molecular endocrinology (Baltimore, Md.), 2008-09, Vol.22 (9), p.2099-2115

2008

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Preparation, Resolution, and Biological Evaluation of 5-Aryl-1,2-dihydro-5H-chromeno[3,4-f]quinolines: Potent, Orally Active, Nonsteroidal Progesterone Receptor Agonists

Journal of medicinal chemistry, 1998-07, Vol.41 (15), p.2779-2785

1998

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Differential Hormone-Dependent Phosphorylation of Progesterone Receptor A and B Forms Revealed by a Phosphoserine Site-Specific Monoclonal Antibody

Molecular endocrinology (Baltimore, Md.), 2000-01, Vol.14 (1), p.52-65

2000

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Novel Series of Potent, Nonsteroidal, Selective Androgen Receptor Modulators Based on 7H-[1,4]Oxazino[3,2-g]quinolin-7-ones

Journal of medicinal chemistry, 2007-05, Vol.50 (10), p.2486-2496

2007

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5-Benzylidene-1,2-dihydrochromeno[3,4-f]quinolines as Selective Progesterone Receptor Modulators

Journal of medicinal chemistry, 2003-09, Vol.46 (19), p.4104-4112

2003

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Steroid receptor family : structure and functions

Endocrine reviews, 1990-05, Vol.11 (2), p.201-220

1990

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Career Choices in the Biosciences: What Companies are Looking for When They are Filling a Position

Experimental biology and medicine (Maywood, N.J.), 2003-12, Vol.228 (11), p.1261-1265

Schrader, William T.

2003

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The mechanism of RU486 antagonism is dependent on the conformation of the carboxy-terminal tail of the human progesterone receptor

Cell, 1992-05, Vol.69 (4), p.703-713

1992

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Potent, nonsteroidal selective androgen receptor modulators (SARMs) based on 8H-[1,4 ]oxazino [2,3 -f] quinolin-8-ones

Bioorganic & medicinal chemistry letters, 2007-10, Vol.17 (19), p.5442-5446

2007

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Development of progesterone receptor antagonists from 1,2-dihydrochromeno[3,4- f]quinoline agonist pharmacophore

Bioorganic & medicinal chemistry letters, 2003-06, Vol.13 (12), p.2075-2078

2003

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Progesterone-binding components of chick oviduct: partial purification and characterization of a calcium-activated protease which hydrolyzes the progesterone receptor

Biochemistry (Easton), 1980-01, Vol.19 (2), p.335-343

1980

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The A and B forms of the chicken progesterone receptor arise by alternate initiation of translation of a unique mRNA

Biochemical and biophysical research communications, 1987-12, Vol.149 (2), p.493-501

1987

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Chicken progesterone receptor expressed in Saccharomyces cerevisiae is correctly phosphorylated at all four Ser-Pro phosphorylation sites

Biochemistry (Easton), 1993-09, Vol.32 (37), p.9563-9569

1993

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Amino acid sequence of a chicken heat shock protein derived from the complementary DNA nucleotide sequence

Biochemistry (Easton), 1986-10, Vol.25 (20), p.6244-6251

1986

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An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis

Scientific reports, 2018-03, Vol.8 (1), p.4730-7, Article 4730

2018

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Sulfhydryl group content of chicken progesterone receptor: effect of oxidation on DNA binding activity

Biochemistry (Easton), 1988-01, Vol.27 (1), p.358-367

1988

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[17] Methods for extraction and quantification of receptors

Methods in Enzymology, 1975, Vol.36, p.187-211

Schrader, William T

1975

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Novel Series of Potent, Nonsteroidal, Selective Androgen Receptor Modulators Based on 7 H -[1,4]Oxazino[3,2- g ]quinolin-7-ones

Journal of medicinal chemistry, 2007-05, Vol.50 (10), p.2486-2496

2007

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Structural analysis of chicken oviduct progesterone receptor using monoclonal antibodies to the subunit B protein

Biochemistry (Easton), 1984-09, Vol.23 (19), p.4427-4435

1984

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Progesterone-binding components of chick oviduct: analysis of receptor structure by limited proteolysis

Biochemistry (Easton), 1980-01, Vol.19 (2), p.343-349

1980

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Interaction of the chick oviduct progesterone receptor with deoxyribonucleic acid

Biochemistry (Easton), 1981-04, Vol.20 (9), p.2481-2491

1981

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Potent, nonsteroidal selective androgen receptor modulators (SARMs) based on 8 H-[1,4]oxazino[2,3- f]quinolin-8-ones

Bioorganic & medicinal chemistry letters, 2007, Vol.17 (19), p.5442-5446

2007

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Discovery of 6-N,N-Bis(2,2,2-trifluoroethyl)amino- 4-trifluoromethylquinolin-2(1H)-one as a Novel Selective Androgen Receptor Modulator

Meclizine Is an Agonist Ligand for Mouse Constitutive Androstane Receptor (CAR) and an Inverse Agonist for Human CAR

Synthesis and biological activity of 5-methylidene 1,2-dihydrochromeno[3,4- f]quinoline derivatives as progesterone receptor modulators

Androgen Receptor-Mediated Apoptosis Is Regulated by Photoactivatable Androgen Receptor Ligands

Preparation, Resolution, and Biological Evaluation of 5-Aryl-1,2-dihydro-5H-chromeno[3,4-f]quinolines: Potent, Orally Active, Nonsteroidal Progesterone Receptor Agonists

Differential Hormone-Dependent Phosphorylation of Progesterone Receptor A and B Forms Revealed by a Phosphoserine Site-Specific Monoclonal Antibody

Novel Series of Potent, Nonsteroidal, Selective Androgen Receptor Modulators Based on 7H-[1,4]Oxazino[3,2-g]quinolin-7-ones

5-Benzylidene-1,2-dihydrochromeno[3,4-f]quinolines as Selective Progesterone Receptor Modulators

Steroid receptor family : structure and functions

Career Choices in the Biosciences: What Companies are Looking for When They are Filling a Position

The mechanism of RU486 antagonism is dependent on the conformation of the carboxy-terminal tail of the human progesterone receptor

Potent, nonsteroidal selective androgen receptor modulators (SARMs) based on 8H-[1,4 ]oxazino [2,3 -f] quinolin-8-ones

Development of progesterone receptor antagonists from 1,2-dihydrochromeno[3,4- f]quinoline agonist pharmacophore

Progesterone-binding components of chick oviduct: partial purification and characterization of a calcium-activated protease which hydrolyzes the progesterone receptor

The A and B forms of the chicken progesterone receptor arise by alternate initiation of translation of a unique mRNA

Chicken progesterone receptor expressed in Saccharomyces cerevisiae is correctly phosphorylated at all four Ser-Pro phosphorylation sites

Amino acid sequence of a chicken heat shock protein derived from the complementary DNA nucleotide sequence

An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis

Sulfhydryl group content of chicken progesterone receptor: effect of oxidation on DNA binding activity

[17] Methods for extraction and quantification of receptors

Novel Series of Potent, Nonsteroidal, Selective Androgen Receptor Modulators Based on 7 H -[1,4]Oxazino[3,2- g ]quinolin-7-ones

Structural analysis of chicken oviduct progesterone receptor using monoclonal antibodies to the subunit B protein

Progesterone-binding components of chick oviduct: analysis of receptor structure by limited proteolysis

Interaction of the chick oviduct progesterone receptor with deoxyribonucleic acid

Potent, nonsteroidal selective androgen receptor modulators (SARMs) based on 8 H-[1,4]oxazino[2,3- f]quinolin-8-ones

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