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British Journal of Clinical Pharmacology
|
November 13, 2021
A randomized study of the safety and pharmacokinetics of GSK3358699, a mononuclear myeloid-targeted bromodomain and extra-terminal domain inhibitor
Jack A Brown, Joanne Bal, Monica Simeoni, et al.
Journal of Medicinal Chemistry
|
January 12, 2016
Discovery of Tetrahydropyrazolopyridine as Sphingosine 1-Phosphate Receptor 3 (S1P3)-Sparing S1P1 Agonists Active at Low Oral Doses
Emmanuel H Demont, James M Bailey, Rino A Bit, et al.
Epigenetics & Chromatin
|
March 8, 2017
Assessing histone demethylase inhibitors in cells: lessons learned
Stephanie B Hatch, Clarence Yapp, Raquel C Montenegro, et al.
Journal of Medicinal Chemistry
|
January 16, 2016
Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives
Susan M Westaway, Alex G S Preston, Michael D Barker, et al.
Journal of Medicinal Chemistry
|
January 16, 2016
Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 1. 3-Amino-4-pyridine Carboxylate Derivatives
Susan M Westaway, Alex G S Preston, Michael D Barker, et al.
Journal of Medicinal Chemistry
|
January 7, 2020
Discovery of a Bromodomain and Extraterminal Inhibitor with a Low Predicted Human Dose through Synergistic Use of Encoded Library Technology and Fragment Screening
Christopher R Wellaway, Dominique Amans, Paul Bamborough, et al.
Journal of Medicinal Chemistry
|
June 12, 2024
Structure- and Property-Based Optimization of Efficient Pan-Bromodomain and Extra Terminal Inhibitors to Identify Oral and Intravenous Candidate I-BET787
David J Hirst, Paul Bamborough, Niam Al-Mahdi, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
British Journal of Clinical Pharmacology
|
November 13, 2021
A randomized study of the safety and pharmacokinetics of GSK3358699, a mononuclear myeloid-targeted bromodomain and extra-terminal domain inhibitor
Jack A Brown, Joanne Bal, Monica Simeoni, et al.
Journal of Medicinal Chemistry
|
January 12, 2016
Discovery of Tetrahydropyrazolopyridine as Sphingosine 1-Phosphate Receptor 3 (S1P3)-Sparing S1P1 Agonists Active at Low Oral Doses
Emmanuel H Demont, James M Bailey, Rino A Bit, et al.
Epigenetics & Chromatin
|
March 8, 2017
Assessing histone demethylase inhibitors in cells: lessons learned
Stephanie B Hatch, Clarence Yapp, Raquel C Montenegro, et al.
Journal of Medicinal Chemistry
|
January 16, 2016
Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives
Susan M Westaway, Alex G S Preston, Michael D Barker, et al.
Journal of Medicinal Chemistry
|
January 16, 2016
Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 1. 3-Amino-4-pyridine Carboxylate Derivatives
Susan M Westaway, Alex G S Preston, Michael D Barker, et al.
Journal of Medicinal Chemistry
|
January 7, 2020
Discovery of a Bromodomain and Extraterminal Inhibitor with a Low Predicted Human Dose through Synergistic Use of Encoded Library Technology and Fragment Screening
Christopher R Wellaway, Dominique Amans, Paul Bamborough, et al.
Journal of Medicinal Chemistry
|
June 12, 2024
Structure- and Property-Based Optimization of Efficient Pan-Bromodomain and Extra Terminal Inhibitors to Identify Oral and Intravenous Candidate I-BET787
David J Hirst, Paul Bamborough, Niam Al-Mahdi, et al.
Page
of 2