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Journal of Medicinal Chemistry
|
January 5, 2024
PROTACs Targeting BRM (SMARCA2) Afford Selective <i>In Vivo</i> Degradation over BRG1 (SMARCA4) and Are Active in BRG1 Mutant Xenograft Tumor Models
Michael Berlin, Jennifer Cantley, Mark Bookbinder, et al.
Journal of Medicinal Chemistry
|
September 29, 2023
Identification of GDC-1971 (RLY-1971), a SHP2 Inhibitor Designed for the Treatment of Solid Tumors
Alexander M Taylor, Bret R Williams, Fabrizio Giordanetto, et al.
Journal of Medicinal Chemistry
|
May 21, 2025
Correction to "PROTACs Targeting BRM (SMARCA2) Afford Selective <i>In Vivo</i> Degradation over BRG1 (SMARCA4) and Are Active in BRG1 Mutant Xenograft Tumor Models"
Michael Berlin, Jennifer Cantley, Mark Bookbinder, et al.
Journal of Medicinal Chemistry
|
September 12, 2017
GNE-781, A Highly Advanced Potent and Selective Bromodomain Inhibitor of Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP)
F Anthony Romero, Jeremy Murray, Kwong Wah Lai, et al.
Journal of Medicinal Chemistry
|
September 30, 2016
Discovery of a Potent and Selective in Vivo Probe (GNE-272) for the Bromodomains of CBP/EP300
Terry D Crawford, F Anthony Romero, Kwong Wah Lai, et al.
Journal of Medicinal Chemistry
|
March 2, 2026
Discovery and Characterization of Divarasib (GDC-6036), a Potent Covalent Inhibitor of KRAS G12C
Nicholas F Endres, Steven Do, Rana Mroue, et al.
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Search research articles
Search
Showing results (101-110 of 106) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 106 results.
Journal of Medicinal Chemistry
|
January 5, 2024
PROTACs Targeting BRM (SMARCA2) Afford Selective <i>In Vivo</i> Degradation over BRG1 (SMARCA4) and Are Active in BRG1 Mutant Xenograft Tumor Models
Michael Berlin, Jennifer Cantley, Mark Bookbinder, et al.
Journal of Medicinal Chemistry
|
September 29, 2023
Identification of GDC-1971 (RLY-1971), a SHP2 Inhibitor Designed for the Treatment of Solid Tumors
Alexander M Taylor, Bret R Williams, Fabrizio Giordanetto, et al.
Journal of Medicinal Chemistry
|
May 21, 2025
Correction to "PROTACs Targeting BRM (SMARCA2) Afford Selective <i>In Vivo</i> Degradation over BRG1 (SMARCA4) and Are Active in BRG1 Mutant Xenograft Tumor Models"
Michael Berlin, Jennifer Cantley, Mark Bookbinder, et al.
Journal of Medicinal Chemistry
|
September 12, 2017
GNE-781, A Highly Advanced Potent and Selective Bromodomain Inhibitor of Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP)
F Anthony Romero, Jeremy Murray, Kwong Wah Lai, et al.
Journal of Medicinal Chemistry
|
September 30, 2016
Discovery of a Potent and Selective in Vivo Probe (GNE-272) for the Bromodomains of CBP/EP300
Terry D Crawford, F Anthony Romero, Kwong Wah Lai, et al.
Journal of Medicinal Chemistry
|
March 2, 2026
Discovery and Characterization of Divarasib (GDC-6036), a Potent Covalent Inhibitor of KRAS G12C
Nicholas F Endres, Steven Do, Rana Mroue, et al.
Page
of 11