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Synthesis and Structure-Activity Relationships of Novel Retinoid X Receptor-Selective Retinoids

Journal of medicinal chemistry, 1994-09, Vol.37 (18), p.2930-2941

1994

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Benzodiazepinone Derivatives Protect against Endoplasmic Reticulum Stress-Mediated Cell Death in Human Neuronal Cell Lines

ACS chemical neuroscience, 2015-03, Vol.6 (3), p.464-475

2015

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Discovery and Preliminary SAR Studies of a Novel, Nonsteroidal Progesterone Receptor Antagonist Pharmacophore

Journal of medicinal chemistry, 1998-08, Vol.41 (18), p.3461-3466

1998

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Similarity of Synthetic Peptide from Human Tumor to Parathyroid Hormone in vivo and in vitro

Science (American Association for the Advancement of Science), 1987-12, Vol.238 (4833), p.1566-1568

1987

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Guanidinylated 2,5-dideoxystreptamine derivatives as anthrax lethal factor inhibitors

Bioorganic & medicinal chemistry letters, 2006-03, Vol.16 (6), p.1527-1531

2006

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Inhibitors of NF-κB and AP-1 Gene Expression: SAR Studies on the Pyrimidine Portion of 2-Chloro-4-trifluoromethylpyrimidine-5-[N-(3‘,5‘-bis(trifluoromethyl)phenyl)carboxamide]

Journal of medicinal chemistry, 2000-10, Vol.43 (21), p.3995-4004

2000

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Cyclic parathyroid hormone-related protein antagonists: lysine 13 to aspartic acid 17 [i to (i + 4)] side chain to side chain lactamization

Biochemistry (Easton), 1991-06, Vol.30 (24), p.5968-5974

1991

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Selectively guanidinylated derivatives of neamine. Syntheses and inhibition of anthrax lethal factor protease

Bioorganic & medicinal chemistry letters, 2006-10, Vol.16 (19), p.5183-5189

2006

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Synthesis and Biological Activity of Novel Nonsteroidal Progesterone Receptor Antagonists Based on Cyclocymopol Monomethyl Ether

Journal of medicinal chemistry, 1996-04, Vol.39 (9), p.1778-1789

1996

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5-Chloro-3-(phenylsulfonyl)indole-2-carboxamide: a novel, non-nucleoside inhibitor of HIV-1 reverse transcriptase

Journal of medicinal chemistry, 1993-04, Vol.36 (9), p.1291-1294

1993

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The human progesterone receptor A-form functions as a transcriptional modulator of mineralocorticoid receptor transcriptional acitivity

The Journal of steroid biochemistry and molecular biology, 1994-04, Vol.48 (5), p.425-432

1994

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Nonsteroidal androgen receptor agonists based on 4-(trifluoromethyl)-2H-pyrano[3,2-g]quinolin-2-one

Bioorganic & medicinal chemistry letters, 1999-04, Vol.9 (7), p.1003-1008

1999

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2-Chloro-4-(trifluoromethyl)pyrimidine-5-N-(3‘,5‘-bis(trifluoromethyl)phenyl)- carboxamide: A Potent Inhibitor of NF-κB- and AP-1-Mediated Gene Expression Identified Using Solution-Phase Combinatorial Chemistry

Journal of medicinal chemistry, 1998-02, Vol.41 (4), p.413-419

1998

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Synthesis of a Series of 4-(Arylethynyl)-6-chloro-4-cyclopropyl-3,4-dihydroquinazolin-2(1H)-ones as Novel Non-nucleoside HIV-1 Reverse Transcriptase Inhibitors

Journal of medicinal chemistry, 1994-07, Vol.37 (15), p.2437-2444

1994

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2-Pyridinone derivatives: a new class of nonnucleoside, HIV-1-specific reverse transcriptase inhibitors

Journal of medicinal chemistry, 1991-09, Vol.34 (9), p.2922-2925

1991

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Preparation and anti-HIV activities of aurintricarboxylic acid fractions and analogs: direct correlation of antiviral potency with molecular weight

Journal of medicinal chemistry, 1991-01, Vol.34 (1), p.329-337

1991

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Nonsteroidal progesterone receptor antagonists based on a conformationally-restricted subseries of 6-aryl-1,2-dihydro-2,2,4-trimethylquinolines

Bioorganic & medicinal chemistry letters, 1998-10, Vol.8 (19), p.2731-2736

1998

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Synthesis and evaluation of 2-pyridinone derivatives as HIV-1 specific reverse transcriptase inhibitors. 1. Phthalimidoalkyl and -alkylamino analogs

Journal of medicinal chemistry, 1992-10, Vol.35 (21), p.3784-3791

1992

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Analysis of estrogen receptor function in vitro reveals three distinct classes of antiestrogens

Molecular endocrinology (Baltimore, Md.), 1995-06, Vol.9 (6), p.659-669

1995

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Human progesterone receptor A form is a cell- and promoter-specific repressor of human progesterone receptor B function

Molecular endocrinology (Baltimore, Md.), 1993-10, Vol.7 (10), p.1244-1255

1993

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Synthesis and anti-HIV activities of low molecular weight aurintricarboxylic acid fragments and related compounds

Journal of medicinal chemistry, 1991-01, Vol.34 (1), p.337-342

1991

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The A and B isoforms of the human progesterone receptor operate through distinct signaling pathways within target cells

Molecular and Cellular Biology, 1994-12, Vol.14 (12), p.8356-8364

1994

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Modifications of position 12 in a parathyroid hormone and parathyroid hormone-related protein: toward the design of highly potent antagonists

Biochemistry (Easton), 1990-02, Vol.29 (6), p.1580-1586

1990

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RU486 exerts antiestrogenic activities through a novel progesterone receptor A form-mediated mechanism

The Journal of biological chemistry, 1994-04, Vol.269 (16), p.11945-11949

1994

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Development of a Nonradioactive, Time-Resolved Fluorescence Assay for the Measurement of Jun N-Terminal Kinase Activity

SLAS discovery, 1997-06, Vol.2 (4), p.213-223

1997

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Synthesis and Structure-Activity Relationships of Novel Retinoid X Receptor-Selective Retinoids

Benzodiazepinone Derivatives Protect against Endoplasmic Reticulum Stress-Mediated Cell Death in Human Neuronal Cell Lines

Discovery and Preliminary SAR Studies of a Novel, Nonsteroidal Progesterone Receptor Antagonist Pharmacophore

Similarity of Synthetic Peptide from Human Tumor to Parathyroid Hormone in vivo and in vitro

Guanidinylated 2,5-dideoxystreptamine derivatives as anthrax lethal factor inhibitors

Inhibitors of NF-κB and AP-1 Gene Expression: SAR Studies on the Pyrimidine Portion of 2-Chloro-4-trifluoromethylpyrimidine-5-[N-(3‘,5‘-bis(trifluoromethyl)phenyl)carboxamide]

Cyclic parathyroid hormone-related protein antagonists: lysine 13 to aspartic acid 17 [i to (i + 4)] side chain to side chain lactamization

Selectively guanidinylated derivatives of neamine. Syntheses and inhibition of anthrax lethal factor protease

Synthesis and Biological Activity of Novel Nonsteroidal Progesterone Receptor Antagonists Based on Cyclocymopol Monomethyl Ether

5-Chloro-3-(phenylsulfonyl)indole-2-carboxamide: a novel, non-nucleoside inhibitor of HIV-1 reverse transcriptase

The human progesterone receptor A-form functions as a transcriptional modulator of mineralocorticoid receptor transcriptional acitivity

Nonsteroidal androgen receptor agonists based on 4-(trifluoromethyl)-2H-pyrano[3,2-g]quinolin-2-one

2-Chloro-4-(trifluoromethyl)pyrimidine-5-N-(3‘,5‘-bis(trifluoromethyl)phenyl)- carboxamide: A Potent Inhibitor of NF-κB- and AP-1-Mediated Gene Expression Identified Using Solution-Phase Combinatorial Chemistry

Synthesis of a Series of 4-(Arylethynyl)-6-chloro-4-cyclopropyl-3,4-dihydroquinazolin-2(1H)-ones as Novel Non-nucleoside HIV-1 Reverse Transcriptase Inhibitors

2-Pyridinone derivatives: a new class of nonnucleoside, HIV-1-specific reverse transcriptase inhibitors

Preparation and anti-HIV activities of aurintricarboxylic acid fractions and analogs: direct correlation of antiviral potency with molecular weight

Nonsteroidal progesterone receptor antagonists based on a conformationally-restricted subseries of 6-aryl-1,2-dihydro-2,2,4-trimethylquinolines

Synthesis and evaluation of 2-pyridinone derivatives as HIV-1 specific reverse transcriptase inhibitors. 1. Phthalimidoalkyl and -alkylamino analogs

Analysis of estrogen receptor function in vitro reveals three distinct classes of antiestrogens

Human progesterone receptor A form is a cell- and promoter-specific repressor of human progesterone receptor B function

Synthesis and anti-HIV activities of low molecular weight aurintricarboxylic acid fragments and related compounds

The A and B isoforms of the human progesterone receptor operate through distinct signaling pathways within target cells

Modifications of position 12 in a parathyroid hormone and parathyroid hormone-related protein: toward the design of highly potent antagonists

RU486 exerts antiestrogenic activities through a novel progesterone receptor A form-mediated mechanism

Development of a Nonradioactive, Time-Resolved Fluorescence Assay for the Measurement of Jun N-Terminal Kinase Activity

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