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Bioorganic & Medicinal Chemistry Letters
|
June 26, 2012
Discovery of novel benzylidene-1,3-thiazolidine-2,4-diones as potent and selective inhibitors of the PIM-1, PIM-2, and PIM-3 protein kinases
Les A Dakin, Michael H Block, Huawei Chen, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 22, 2018
Discovery of 2,6-disubstituted pyrazine derivatives as inhibitors of CK2 and PIM kinases
Lakshmaiah Gingipalli, Michael H Block, Larry Bao, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 20, 2016
Discovery of cofactor-specific, bactericidal Mycobacterium tuberculosis InhA inhibitors using DNA-encoded library technology
Holly H Soutter, Paolo Centrella, Matthew A Clark, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 29, 2015
Identification of azabenzimidazoles as potent JAK1 selective inhibitors
Melissa M Vasbinder, Marat Alimzhanov, Martin Augustin, et al.
Journal of Medicinal Chemistry
|
May 6, 2021
Discovery of Novel, Potent Inhibitors of Hydroxy Acid Oxidase 1 (HAO1) Using DNA-Encoded Chemical Library Screening
Esther C Y Lee, Andrew J McRiner, Katy E Georgiadis, et al.
Journal of the Society for Cardiovascular Angiography & Interventions
|
August 12, 2024
Femoral Artery Closure Devices vs Manual Compression During Cardiac Catheterization and Percutaneous Coronary Intervention
Rolf P Kreutz, Sujoy Phookan, Hamid Bahrami, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 8, 2015
Discovery of AZ0108, an orally bioavailable phthalazinone PARP inhibitor that blocks centrosome clustering
Jeffrey W Johannes, Lynsie Almeida, Kevin Daly, et al.
Journal of Medicinal Chemistry
|
June 2, 2018
Discovery and Optimization of a Novel Series of Highly Selective JAK1 Kinase Inhibitors
Neil P Grimster, Erica Anderson, Marat Alimzhanov, et al.
Chemmedchem
|
December 22, 2017
Structure-Based Design of Selective Noncovalent CDK12 Inhibitors
Jeffrey W Johannes, Christopher R Denz, Nancy Su, et al.
Journal of Medicinal Chemistry
|
April 17, 2020
Discovery of (2<i>R</i>)-<i>N</i>-[3-[2-[(3-Methoxy-1-methyl-pyrazol-4-yl)amino]pyrimidin-4-yl]-1<i>H</i>-indol-7-yl]-2-(4-methylpiperazin-1-yl)propenamide (AZD4205) as a Potent and Selective Janus Kinase 1 Inhibitor
Qibin Su, Erica Banks, Geraldine Bebernitz, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 49) with videos related to
Sort By:
Page
of 5
Bioorganic & Medicinal Chemistry Letters
|
June 26, 2012
Discovery of novel benzylidene-1,3-thiazolidine-2,4-diones as potent and selective inhibitors of the PIM-1, PIM-2, and PIM-3 protein kinases
Les A Dakin, Michael H Block, Huawei Chen, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 22, 2018
Discovery of 2,6-disubstituted pyrazine derivatives as inhibitors of CK2 and PIM kinases
Lakshmaiah Gingipalli, Michael H Block, Larry Bao, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 20, 2016
Discovery of cofactor-specific, bactericidal Mycobacterium tuberculosis InhA inhibitors using DNA-encoded library technology
Holly H Soutter, Paolo Centrella, Matthew A Clark, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 29, 2015
Identification of azabenzimidazoles as potent JAK1 selective inhibitors
Melissa M Vasbinder, Marat Alimzhanov, Martin Augustin, et al.
Journal of Medicinal Chemistry
|
May 6, 2021
Discovery of Novel, Potent Inhibitors of Hydroxy Acid Oxidase 1 (HAO1) Using DNA-Encoded Chemical Library Screening
Esther C Y Lee, Andrew J McRiner, Katy E Georgiadis, et al.
Journal of the Society for Cardiovascular Angiography & Interventions
|
August 12, 2024
Femoral Artery Closure Devices vs Manual Compression During Cardiac Catheterization and Percutaneous Coronary Intervention
Rolf P Kreutz, Sujoy Phookan, Hamid Bahrami, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 8, 2015
Discovery of AZ0108, an orally bioavailable phthalazinone PARP inhibitor that blocks centrosome clustering
Jeffrey W Johannes, Lynsie Almeida, Kevin Daly, et al.
Journal of Medicinal Chemistry
|
June 2, 2018
Discovery and Optimization of a Novel Series of Highly Selective JAK1 Kinase Inhibitors
Neil P Grimster, Erica Anderson, Marat Alimzhanov, et al.
Chemmedchem
|
December 22, 2017
Structure-Based Design of Selective Noncovalent CDK12 Inhibitors
Jeffrey W Johannes, Christopher R Denz, Nancy Su, et al.
Journal of Medicinal Chemistry
|
April 17, 2020
Discovery of (2<i>R</i>)-<i>N</i>-[3-[2-[(3-Methoxy-1-methyl-pyrazol-4-yl)amino]pyrimidin-4-yl]-1<i>H</i>-indol-7-yl]-2-(4-methylpiperazin-1-yl)propenamide (AZD4205) as a Potent and Selective Janus Kinase 1 Inhibitor
Qibin Su, Erica Banks, Geraldine Bebernitz, et al.
Page
of 5