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Hepatoselectivity of statins: Design and synthesis of 4-sulfamoyl pyrroles as HMG-CoA reductase inhibitors

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (3), p.1151-1156

2008

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In silico screening for compounds that match the pharmacophore of omega-hexatoxin-Hv1a leads to discovery and optimization of a novel class of insecticides

Pesticide biochemistry and physiology, 2013-07, Vol.106 (3), p.124-140

2013

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Evaluation of Physicochemical Parameters Important to the Oral Bioavailability of Peptide-like Compounds: Implications for the Synthesis of Renin Inhibitors

Journal of medicinal chemistry, 1995-04, Vol.38 (9), p.1446-1455

1995

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Design and Synthesis of Renin Inhibitors: Incorporation of Transition-State Isostere Side Chains That Span from the S1 to the S3 Binding Pockets and Examination of P3-Modified Renin Inhibitors

Journal of medicinal chemistry, 1995-07, Vol.38 (15), p.2893-2905

1995

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Structure-activity relationships of a series of 2-amino-4-thiazole-containing renin inhibitors

Journal of medicinal chemistry, 1992-07, Vol.35 (14), p.2562-2572

1992

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Comparison of intestinal permeabilities determined in multiple in vitro and in situ models : relationship to absorption in humans

Pharmaceutical research, 1995-05, Vol.12 (5), p.693-699

1995

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Synthesis of 5,6-Dihydro-4-hydroxy-2- pyrones as HIV-1 Protease Inhibitors: The Profound Effect of Polarity on Antiviral Activity

Journal of medicinal chemistry, 1997-11, Vol.40 (23), p.3707-3711

1997

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SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF NOVEL AMINOTHIAZOLYL β-LACTAM DERIVATIVES

The Journal of Antibiotics, 1986, Vol.39(3), pp.372-379

1986

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Nonpeptidic HIV protease inhibitors possessing excellent antiviral activities and therapeutic indices. PD 178390 : A lead HIV protease inhibitor

Bioorganic & medicinal chemistry, 1999-12, Vol.7 (12), p.2775-2800

1999

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A topliss tree analysis of the HIV-protease inhibitory activity of 6-phenyl-4-hydroxy-pyran-2-ones

Bioorganic & medicinal chemistry letters, 1996-05, Vol.6 (10), p.1099-1104

1996

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synthesis of Enantiomerically Pure amino acids containing a 2-Amino-4-thiazolyl side chain

Synthetic communications, 1990-11, Vol.20 (20), p.3097-3102

1990

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Pharmacological Differences Between Rat and Human Endothelin B Receptors

Biochemical and biophysical research communications, 1995-04, Vol.209 (2), p.506-512

1995

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THE TOTAL SYNTHESIS OF AWAITIN A, A CITRIC ACID BASED SIDEROPHORE

STEINBAUGH, BRUCE ALLAN

1985

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Hepatoselectivity of statins: Design and synthesis of 4-sulfamoyl pyrroles as HMG-CoA reductase inhibitors

In silico screening for compounds that match the pharmacophore of omega-hexatoxin-Hv1a leads to discovery and optimization of a novel class of insecticides

Evaluation of Physicochemical Parameters Important to the Oral Bioavailability of Peptide-like Compounds: Implications for the Synthesis of Renin Inhibitors

Design and Synthesis of Renin Inhibitors: Incorporation of Transition-State Isostere Side Chains That Span from the S1 to the S3 Binding Pockets and Examination of P3-Modified Renin Inhibitors

Structure-activity relationships of a series of 2-amino-4-thiazole-containing renin inhibitors

Comparison of intestinal permeabilities determined in multiple in vitro and in situ models : relationship to absorption in humans

Synthesis of 5,6-Dihydro-4-hydroxy-2- pyrones as HIV-1 Protease Inhibitors: The Profound Effect of Polarity on Antiviral Activity

SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF NOVEL AMINOTHIAZOLYL β-LACTAM DERIVATIVES

Nonpeptidic HIV protease inhibitors possessing excellent antiviral activities and therapeutic indices. PD 178390 : A lead HIV protease inhibitor

A topliss tree analysis of the HIV-protease inhibitory activity of 6-phenyl-4-hydroxy-pyran-2-ones

synthesis of Enantiomerically Pure amino acids containing a 2-Amino-4-thiazolyl side chain

Pharmacological Differences Between Rat and Human Endothelin B Receptors

THE TOTAL SYNTHESIS OF AWAITIN A, A CITRIC ACID BASED SIDEROPHORE

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