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Design and synthesis of orally bioavailable serum and glucocorticoid-regulated kinase 1 (SGK1) inhibitors

Bioorganic & medicinal chemistry letters, 2009-08, Vol.19 (15), p.4441-4445

2009

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Rational design of orally-active, pyrrolidine-based progesterone receptor partial agonists

Bioorganic & medicinal chemistry letters, 2009-08, Vol.19 (16), p.4777-4780

2009

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Improving the developability profile of pyrrolidine progesterone receptor partial agonists

Bioorganic & medicinal chemistry letters, 2010-01, Vol.20 (1), p.371-374

2010

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Discovery of orally active, pyrrolidinone-based progesterone receptor partial agonists

Bioorganic & medicinal chemistry letters, 2009-08, Vol.19 (16), p.4664-4668

2009

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Multisubstrate inhibitors of dopamine .beta.-hydroxylase. 1. Some 1-phenyl and 1-phenyl-bridged derivatives of imidazole-2-thione

Journal of medicinal chemistry, 1986-12, Vol.29 (12), p.2465-2472

1986

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Synthesis and antiviral activity of a novel class of HIV-1 protease inhibitors containing a heterocyclic P1′-P2′ amide bond isostere

Bioorganic & medicinal chemistry letters, 1994-10, Vol.4 (20), p.2441-2446

1994

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Orally Active and Potent Inhibitors of γ-Aminobutyric Acid Uptake

Journal of medicinal chemistry, 1985-05, Vol.28 (5), p.653-660

1985

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Some benzyl-substituted imidazoles, triazoles, tetrazoles, pyridinethiones, and structural relatives as multisubstrate inhibitors of dopamine .beta.-hydroxylase. 4. Structure-activity relationships at the copper binding site

Journal of medicinal chemistry, 1990-02, Vol.33 (2), p.781-789

1990

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High-affinity leukotriene receptor antagonists. Synthesis and pharmacological characterization of 2-hydroxy-3-[(2-carboxyethyl)thio]-3-[2-(8-phenyloctyl)phenyl]propanoic acid

Journal of medicinal chemistry, 1987-06, Vol.30 (6), p.959-961

1987

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Multisubstrate inhibitors of dopamine .beta.-hydroxylase. 2. Structure-activity relationships at the phenethylamine binding site

Journal of medicinal chemistry, 1987-03, Vol.30 (3), p.486-494

1987

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SB 209670, a Rationally Designed Potent Nonpeptide Endothelin Receptor Antagonist

Proceedings of the National Academy of Sciences - PNAS, 1994-08, Vol.91 (17), p.8052-8056

1994

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Substituted 1-benzylimidazole-2-thiols as potent and orally active inhibitors of dopamine .beta.-hydroxylase

Journal of medicinal chemistry, 1986-06, Vol.29 (6), p.887-889

1986

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3-Phenyl-5-quinolinemethanol antimalarials

Journal of medicinal chemistry, 1973-02, Vol.16 (2), p.118-122

1973

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Adrenergic agents. 6. Synthesis and potential .beta.-adrenergic agonist activity of some meta-substituted p-hydroxyphenylethanolamines related to salbutamol

Journal of medicinal chemistry, 1977-08, Vol.20 (8), p.1029-1035

1977

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Adrenergic agents. 8. Synthesis and .beta.-adrenergic agonist activity of some 3-tert-butylamino-2-(substituted phenyl)-1-propanols

Journal of medicinal chemistry, 1977-10, Vol.20 (10), p.1263-1268

1977

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Synthesis and antiviral activity of a novel class of HIV-1 protease inhibitors containing a heterocyclic P 1′-P 2′ amide bond isostere

Bioorganic & medicinal chemistry letters, 1994-10, Vol.4 (20), p.2441-2446

1994

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Adrenergic Agents. 7. Synthesis and β-Adrenergic Agonist Activity of Several 2-Pyridylethanolamines

Journal of medicinal chemistry, 1977-10, Vol.20 (10), p.1258-1262

1977

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Inhibitors of Phenylethanolamine N-Methyltransferase and Epinephrine Biosynthesis: A Potential Source of New Drugs

Drug metabolism reviews, 1983, Vol.14 (4), p.709-721

1983

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When small words foretell academic success: the case of college admissions essays

PloS one, 2014-12, Vol.9 (12), p.e115844-e115844

2014

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A roadmap for urban evolutionary ecology

Evolutionary applications, 2019-03, Vol.12 (3), p.384-398

2019

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Enhancing Nursing Education Through Affordable and Realistic Holographic Mixed Reality: The Virtual Standardized Patient for Clinical Simulation

Advances in experimental medicine and biology, 2019, Vol.1120, p.1-13

2019

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HIV Screening in an Urban Emergency Department: Comparison of Screening Using an Opt-In Versus an Opt-Out Approach

Annals of emergency medicine, 2011-07, Vol.58 (1), p.S89-S95

2011

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Temperature dependence of the reactions of Cl with toluene and the xylenes

International journal of chemical kinetics, 2019-08, Vol.51 (8), p.579-589

2019

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Estimating renal function for drug dosing in critically ill patients with persistent inflammation, immunosuppression and catabolism syndrome

Internal and emergency medicine, 2021-10, Vol.16 (7), p.1751-1753

2021

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Design and synthesis of orally bioavailable serum and glucocorticoid-regulated kinase 1 (SGK1) inhibitors

Rational design of orally-active, pyrrolidine-based progesterone receptor partial agonists

Improving the developability profile of pyrrolidine progesterone receptor partial agonists

Discovery of orally active, pyrrolidinone-based progesterone receptor partial agonists

Multisubstrate inhibitors of dopamine .beta.-hydroxylase. 1. Some 1-phenyl and 1-phenyl-bridged derivatives of imidazole-2-thione

Synthesis and antiviral activity of a novel class of HIV-1 protease inhibitors containing a heterocyclic P1′-P2′ amide bond isostere

Orally Active and Potent Inhibitors of γ-Aminobutyric Acid Uptake

Some benzyl-substituted imidazoles, triazoles, tetrazoles, pyridinethiones, and structural relatives as multisubstrate inhibitors of dopamine .beta.-hydroxylase. 4. Structure-activity relationships at the copper binding site

High-affinity leukotriene receptor antagonists. Synthesis and pharmacological characterization of 2-hydroxy-3-[(2-carboxyethyl)thio]-3-[2-(8-phenyloctyl)phenyl]propanoic acid

Multisubstrate inhibitors of dopamine .beta.-hydroxylase. 2. Structure-activity relationships at the phenethylamine binding site

SB 209670, a Rationally Designed Potent Nonpeptide Endothelin Receptor Antagonist

Substituted 1-benzylimidazole-2-thiols as potent and orally active inhibitors of dopamine .beta.-hydroxylase

3-Phenyl-5-quinolinemethanol antimalarials

Adrenergic agents. 6. Synthesis and potential .beta.-adrenergic agonist activity of some meta-substituted p-hydroxyphenylethanolamines related to salbutamol

Adrenergic agents. 8. Synthesis and .beta.-adrenergic agonist activity of some 3-tert-butylamino-2-(substituted phenyl)-1-propanols

Synthesis and antiviral activity of a novel class of HIV-1 protease inhibitors containing a heterocyclic P 1′-P 2′ amide bond isostere

Adrenergic Agents. 7. Synthesis and β-Adrenergic Agonist Activity of Several 2-Pyridylethanolamines

Inhibitors of Phenylethanolamine N-Methyltransferase and Epinephrine Biosynthesis: A Potential Source of New Drugs

When small words foretell academic success: the case of college admissions essays

PSMA-targeting TGFβ-insensitive armored CAR T cells in metastatic castration-resistant prostate cancer: a phase 1 trial

A roadmap for urban evolutionary ecology

Enhancing Nursing Education Through Affordable and Realistic Holographic Mixed Reality: The Virtual Standardized Patient for Clinical Simulation

HIV Screening in an Urban Emergency Department: Comparison of Screening Using an Opt-In Versus an Opt-Out Approach

Temperature dependence of the reactions of Cl with toluene and the xylenes

Estimating renal function for drug dosing in critically ill patients with persistent inflammation, immunosuppression and catabolism syndrome

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