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Chemistry

D-Index
55
Citations
9256
World Ranking
12303
National Ranking
904

Overview

Joel C. Barrish is affiliated with Bristol-Myers Squibb (Germany) in Germany. Their research spans multiple fields including Biochemistry, Genetics and Molecular Biology, as well as Medicine.

The scientist's work covers a variety of subfields such as Materials Chemistry, Molecular Biology, Biochemistry, Surgery, and Endocrinology, Diabetes and Metabolism.

Main topics in their research include

  • Amino Acid Enzymes and Metabolism
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Metabolism and Genetic Disorders
  • Pancreatic function and diabetes
  • Diabetes Treatment and Management
  • Biochemical and Molecular Research

Joel C. Barrish has contributed to a range of recent publications, including the following:

  • BMS-813160: A Potent CCR2 and CCR5 Dual Antagonist Selected as a Clinical Candidate (2021), published in ACS Medicinal Chemistry Letters
  • Optimization of Nicotinamides as Potent and Selective IRAK4 Inhibitors with Efficacy in a Murine Model of Psoriasis (2020), published in ACS Medicinal Chemistry Letters
  • Discovery of a Partial Glucokinase Activator Clinical Candidate: Diethyl ((3-(3-((5-(Azetidine-1-carbonyl)pyrazin-2-yl)oxy)-5-isopropoxybenzamido)-1H-pyrazol-1-yl)methyl)phosphonate (BMS-820132) (2022), published in Journal of Medicinal Chemistry
  • SLC6A19 inhibition facilitates urinary neutral amino acid excretion and lowers plasma phenylalanine (2024), published in JCI Insight
  • Driving Potency with Rotationally Stable Atropisomers: Discovery of Pyridopyrimidinedione-Carbazole Inhibitors of BTK (2020), published in ACS Medicinal Chemistry Letters

Frequent co-authors of Joel C. Barrish include

  • Arvind Mathur
  • Percy H. Carter
  • Nick Pullen
  • Dean G. Brown
  • Dauh-Rurng Wu

They publish regularly in venues such as

  • The Cambridge Structural Database
  • ACS Medicinal Chemistry Letters
  • Molecular Genetics and Metabolism
  • Journal of Medicinal Chemistry
  • JCI Insight

Best Publications

  • Discovery of N-(2-chloro-6-methyl- phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4- ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays.

    Louis J. Lombardo;Francis Y. Lee;Ping Chen;Derek Norris

  • 2-aminothiazole as a novel kinase inhibitor template. Structure-activity relationship studies toward the discovery of N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1- piperazinyl)]-2-methyl-4-pyrimidinyl]amino)]-1,3-thiazole-5-carboxamide (dasatinib, BMS-354825) as a potent pan-Src kinase inhibitor.

    Jagabandhu Das;Ping Chen;Derek Norris;Ramesh Padmanabha

  • Cyclic protein tyrosine kinase inhibitors

    Jagabandhu Das;Ramesh Padmanabha;Ping Chen;Derek J. Norris

  • A new facile method for the synthesis of 1-arylimidazole-5-carboxylates

    Bang-Chi Chen;Mark S Bednarz;Rulin Zhao;Joseph E Sundeen

  • A stereoselective synthesis of 1,3-diol derivatives and application to the ansa bridge of rifamycin S

    W. Clark Still;Joel C. Barrish

  • Discovery and preclinical studies of (R)-1-(4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-5- methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)propan- 2-ol (BMS-540215), an in vivo active potent VEGFR-2 inhibitor.

    Rajeev S. Bhide;Zhen-Wei Cai;Yong-Zheng Zhang;Ligang Qian

  • Discovery of brivanib alaninate ((S)-((R)-1-(4-(4-fluoro-2-methyl-1H-indol-5-yloxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)propan-2-yl)2-aminopropanoate), a novel prodrug of dual vascular endothelial growth factor receptor-2 and fibroblast growth factor receptor-1 kinase inhibitor (BMS-540215).

    Zhen-wei Cai;Yongzheng Zhang;Robert M. Borzilleri;Ligang Qian

  • Selective Itk Inhibitors Block T-Cell Activation and Murine Lung Inflammation

    Tai An Lin;Kim W. McIntyre;Jagabandhu Das;Chunjian Liu

  • Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56lck inhibitors

    Jagabandhu Das;Robert V. Moquin;James Lin;Chunjian Liu

  • Discovery of 6-Fluoro-5-(R)-(3-(S)-(8-fluoro-1-methyl-2,4-dioxo-1,2-dihydroquinazolin-3(4H)-yl)-2-methylphenyl)-2-(S)-(2-hydroxypropan-2-yl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide (BMS-986142): A Reversible Inhibitor of Bruton's Tyrosine Kinase (BTK) Conformationally Constrained by Two Locked Atropisomers.

    Scott H. Watterson;George V. De Lucca;Qing Shi;Charles M. Langevine

  • METHODS OF TREATING p38 KINASE-ASSOCIATED CONDITIONS AND PYRROLOTRIAZINE COMPOUNDS USEFUL AS KINASE INHIBITORS

    Katerina Leftheris;Joel Barrish;John Hynes;Stephen T. Wrobleski

  • Heterocyclo-substituted imidazopyrazine protein tyrosine kinase inhibitors

    Ping Chen;Derek J. Norris;Joel C. Barrish;Edwin J. Iwanowicz

  • Discovery and SAR of 2-amino-5-(thioaryl)thiazoles as potent and selective Itk inhibitors.

    Jagabandhu Das;Joseph A. Furch;Chunjian Liu;Robert V. Moquin

  • Design, synthesis, and anti-inflammatory properties of orally active 4-(phenylamino)-pyrrolo[2,1-f][1,2,4]triazine p38alpha mitogen-activated protein kinase inhibitors.

    John Hynes;Alaric J. Dyckman;Shuqun Lin;Stephen T. Wrobleski

  • Dual action inhibitors

    Donald S. Karanewsky;Joel C. Barrish;Edward W. Petrillo;Jeffrey A. Robl

  • Amino Diol HIV Protease Inhibitors. 1. Design, Synthesis, and Preliminary SAR

    Joel C. Barrish;Eric Gordon;Masud Alam;Pin-Fang Lin

  • 5-Cyanopyrimidine derivatives as a novel class of potent, selective, and orally active inhibitors of p38alpha MAP kinase.

    Chunjian Liu;Stephen T. Wrobleski;James Lin;Gulzar Ahmed

  • Cupric bromide mediated oxidation of 4-carboxyoxazolines to the corresponding oxazoles

    Joel C. Barrish;Janak Singh;Steven H. Spergel;Wen Ching Han

  • Substituted biphenyl sulfonamide endothelin antagonists

    Natesan Murugesan;Joel C. Barrish;Philip D. Stein

  • Imidazoquinoxaline protein tyrosine kinase inhibitors

    Joel C. Barrish;Ping Chen;Jagabandhu Das;Edwin J. Iwanowicz

Frequent Co-Authors

Gary L. Schieven
Gary L. Schieven Genesis Biotechnology Group
John T. Hunt
John T. Hunt Bristol-Myers Squibb (Germany)
Diane Hollenbaugh
Diane Hollenbaugh Bonum Therapeutics
James R. Burke
James R. Burke Duke University

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