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Synthetic studies toward a simplified eleuthoside core

Medicinal chemistry research, 2023-07, Vol.32 (7), p.1376-1382

2023

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Potent Inhibitors of Hepatitis C Virus NS3 Protease: Employment of a Difluoromethyl Group as a Hydrogen-Bond Donor

ACS medicinal chemistry letters, 2018-02, Vol.9 (2), p.143-148

2018

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The discovery and evaluation of [18F]BMS-986229, a novel macrocyclic peptide PET radioligand for the measurement of PD-L1 expression and in-vivo PD-L1 target engagement

European journal of nuclear medicine and molecular imaging, 2024-03, Vol.51 (4), p.978-990

2024

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Discovery and Early Clinical Evaluation of BMS-605339, a Potent and Orally Efficacious Tripeptidic Acylsulfonamide NS3 Protease Inhibitor for the Treatment of Hepatitis C Virus Infection

Journal of medicinal chemistry, 2014-03, Vol.57 (5), p.1708-1729

2014

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Development, Characterization, and Radiation Dosimetry Studies of 18F-BMS-986229, a 18F-Labeled PD-L1 Macrocyclic Peptide PET Tracer

Molecular imaging and biology, 2024-04, Vol.26 (2), p.301-309

2024

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Room‐Temperature Copper‐Catalyzed Etherification of Aryl Bromides

Angewandte Chemie, 2024-05, Vol.136 (19), p.n/a

2024

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Identification of a Potent and Selective 5-HT6 Antagonist: One-Step Synthesis of (E)-3-(Benzenesulfonyl)-2- (methylsulfanyl)pyrido[1,2-a]pyrimidin- 4-ylidenamine from 2-(Benzenesulfonyl)-3,3- bis(methylsulfanyl)acrylonitrile

Journal of medicinal chemistry, 2003-11, Vol.46 (23), p.4834-4837

2003

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The Discovery of Asunaprevir (BMS-650032), An Orally Efficacious NS3 Protease Inhibitor for the Treatment of Hepatitis C Virus Infection

Journal of medicinal chemistry, 2014-03, Vol.57 (5), p.1730-1752

2014

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Discovery of a Potent Acyclic, Tripeptidic, Acyl Sulfonamide Inhibitor of Hepatitis C Virus NS3 Protease as a Back-up to Asunaprevir with the Potential for Once-Daily Dosing

Journal of medicinal chemistry, 2016-09, Vol.59 (17), p.8042-8060

2016

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Development, Characterization, and Radiation Dosimetry Studies of 18 F-BMS-986229, a 18 F-Labeled PD-L1 Macrocyclic Peptide PET Tracer

Molecular imaging and biology, 2024-04, Vol.26 (2), p.301

2024

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N-acyl imines and related hetero dienes in [4+2]-cycloaddition reactions

Chemical reviews, 1989-11, Vol.89 (7), p.1525-1534

1989

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The Discovery and Early Clinical Evaluation of the HCV NS3/4A Protease Inhibitor Asunaprevir (BMS-650032)

HCV: The Journey from Discovery to a Cure, 2019, p.317-354

2019

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Chapter 14. Antiviral agents

Annual Reports in Medicinal Chemistry, 2002, Vol.37, p.133-147

2002

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Identification of a potent and selective 5-HT(6) antagonist: one-step synthesis of (E)-3-(benzenesulfonyl)-2- (methylsulfanyl)pyrido[1,2-a]pyrimidin-4-ylidenamine from 2-(benzenesulfonyl)-3,3-bis(methylsulfanyl)acrylonitrile

Journal of medicinal chemistry, 2003-11, Vol.46 (23), p.4834

2003

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Identification of a Potent and Selective 5-HT 6 Antagonist: One-Step Synthesis of ( E )-3-(Benzenesulfonyl)-2- (methylsulfanyl)pyrido[1,2- a ]pyrimidin- 4-ylidenamine from 2-(Benzenesulfonyl)-3,3- bis(methylsulfanyl)acrylonitrile

Journal of medicinal chemistry, 2003-11, Vol.46 (23), p.4834-4837

2003

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Anodic Dimerization of 1,2,3,4-Tetrahydrocabazole and Some of Its Derivatives

Heterocycles, 1986, Vol.24 (3), p.669

1986

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Chapter 20 Progress towards the Discovery and Development of Specifically Targeted Inhibitors of Hepatitis C Virus

Annual Reports in Medicinal Chemistry, 2009, Vol.44, p.397-440

2009

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A Facile Synthesis of 1-Substituted Cyclopropylsulfonamides

ChemInform, 2006-07, Vol.37 (30), p.no-no

2006

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Developments in antiviral drug design, discovery and development in 2004

Current drug targets. Infectious disorders, 2005-12, Vol.5 (4), p.307-400

2005

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Ultrastructural Characterization of the Giant Volcano-like Virus Factory of Acanthamoeba polyphaga Mimivirus

PloS one, 2007-03, Vol.2 (3), p.e328-e328

2007

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The planar polarity gene strabismus regulates convergent extension movements in Xenopus

The EMBO journal, 2002-03, Vol.21 (5), p.976-985

2002

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Conductor Design of the Madmax 9 T Large Dipole Magnet

IEEE transactions on applied superconductivity, 2020-06, Vol.30 (4), p.1-1

2020

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Steroid Pulse Therapy for Severe Central Nervous System Involvement in Shiga Toxin-Producing Escherichia coli-Related Hemolytic Uremic Syndrome

Case reports in pediatrics, 2021-05, Vol.2021, p.1-4

2021

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Lipid peroxidation biomarkers in adolescents with or at high-risk for bipolar disorder

Journal of affective disorders, 2016-03, Vol.192, p.176-183

2016

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Synthetic studies toward a simplified eleuthoside core

Potent Inhibitors of Hepatitis C Virus NS3 Protease: Employment of a Difluoromethyl Group as a Hydrogen-Bond Donor

The discovery and evaluation of [18F]BMS-986229, a novel macrocyclic peptide PET radioligand for the measurement of PD-L1 expression and in-vivo PD-L1 target engagement

Discovery and Early Clinical Evaluation of BMS-605339, a Potent and Orally Efficacious Tripeptidic Acylsulfonamide NS3 Protease Inhibitor for the Treatment of Hepatitis C Virus Infection

Development, Characterization, and Radiation Dosimetry Studies of 18F-BMS-986229, a 18F-Labeled PD-L1 Macrocyclic Peptide PET Tracer

Room‐Temperature Copper‐Catalyzed Etherification of Aryl Bromides

Identification of a Potent and Selective 5-HT6 Antagonist: One-Step Synthesis of (E)-3-(Benzenesulfonyl)-2- (methylsulfanyl)pyrido[1,2-a]pyrimidin- 4-ylidenamine from 2-(Benzenesulfonyl)-3,3- bis(methylsulfanyl)acrylonitrile

The Discovery of Asunaprevir (BMS-650032), An Orally Efficacious NS3 Protease Inhibitor for the Treatment of Hepatitis C Virus Infection

Discovery of BMS-986144, a Third-Generation, Pan-Genotype NS3/4A Protease Inhibitor for the Treatment of Hepatitis C Virus Infection

Discovery of a Potent Acyclic, Tripeptidic, Acyl Sulfonamide Inhibitor of Hepatitis C Virus NS3 Protease as a Back-up to Asunaprevir with the Potential for Once-Daily Dosing

Development, Characterization, and Radiation Dosimetry Studies of 18 F-BMS-986229, a 18 F-Labeled PD-L1 Macrocyclic Peptide PET Tracer

N-acyl imines and related hetero dienes in [4+2]-cycloaddition reactions

The Discovery and Early Clinical Evaluation of the HCV NS3/4A Protease Inhibitor Asunaprevir (BMS-650032)

Chapter 14. Antiviral agents

Identification of a potent and selective 5-HT(6) antagonist: one-step synthesis of (E)-3-(benzenesulfonyl)-2- (methylsulfanyl)pyrido[1,2-a]pyrimidin-4-ylidenamine from 2-(benzenesulfonyl)-3,3-bis(methylsulfanyl)acrylonitrile

Identification of a Potent and Selective 5-HT 6 Antagonist: One-Step Synthesis of ( E )-3-(Benzenesulfonyl)-2- (methylsulfanyl)pyrido[1,2- a ]pyrimidin- 4-ylidenamine from 2-(Benzenesulfonyl)-3,3- bis(methylsulfanyl)acrylonitrile

Anodic Dimerization of 1,2,3,4-Tetrahydrocabazole and Some of Its Derivatives

Chapter 20 Progress towards the Discovery and Development of Specifically Targeted Inhibitors of Hepatitis C Virus

A Facile Synthesis of 1-Substituted Cyclopropylsulfonamides

Developments in antiviral drug design, discovery and development in 2004

Ultrastructural Characterization of the Giant Volcano-like Virus Factory of Acanthamoeba polyphaga Mimivirus

The planar polarity gene strabismus regulates convergent extension movements in Xenopus

Conductor Design of the Madmax 9 T Large Dipole Magnet

Steroid Pulse Therapy for Severe Central Nervous System Involvement in Shiga Toxin-Producing Escherichia coli-Related Hemolytic Uremic Syndrome

Lipid peroxidation biomarkers in adolescents with or at high-risk for bipolar disorder

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