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John G Allen

Showing results (11-20 of 19) with videos related to

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The Journal of Organic Chemistry|May 7, 2016
Telescoped Process to Manufacture 6,6,6-Trifluorofucose via Diastereoselective Transfer Hydrogenation: Scalable Access to an Inhibitor of Fucosylation Utilized in Monoclonal Antibody ProductionMichal M Achmatowicz, John G Allen, Matthew M Bio, et al.
Chemical Research in Toxicology|January 26, 2010
Cytochrome P450-mediated epoxidation of 2-aminothiazole-based AKT inhibitors: identification of novel GSH adducts and reduction of metabolic activation through structural changes guided by in silico and in vitro screeningRaju Subramanian, Matthew R Lee, John G Allen, et al.
Journal of Medicinal Chemistry|November 21, 2023
Imidazolone as an Amide Bioisostere in the Development of β-1,3-<i>N</i>-Acetylglucosaminyltransferase 2 (B3GNT2) InhibitorsJeffrey J Jackson, Aaron C Siegmund, Wen-Ju Bai, et al.
Bioorganic & Medicinal Chemistry Letters|October 15, 2013
The optimization of aminooxadiazoles as orally active inhibitors of Cdc7Paul E Harrington, Matthew P Bourbeau, Christopher Fotsch, et al.
ACS Chemical Biology|July 20, 2016
Facile Modulation of Antibody Fucosylation with Small Molecule Fucostatin Inhibitors and Cocrystal Structure with GDP-Mannose 4,6-DehydrataseJohn G Allen, Mirna Mujacic, Michael J Frohn, et al.
Journal of Medicinal Chemistry|October 28, 2009
Discovery and optimization of chromenotriazolopyrimidines as potent inhibitors of the mouse double minute 2-tumor protein 53 protein-protein interactionJohn G Allen, Matthew P Bourbeau, G Erich Wohlhieter, et al.
Bioorganic & Medicinal Chemistry Letters|February 9, 2010
Azole-based inhibitors of AKT/PKB for the treatment of cancerQingping Zeng, John G Allen, Matthew P Bourbeau, et al.
Journal of Medicinal Chemistry|July 14, 2026
Expanding Addressable KRAS Mutations through the Structure- and Property-Based Design of Dual-State (GDP/GTP), Reversible Pan-KRAS InhibitorsRyan P Wurz, Jennifer R Allen, John G Allen, et al.
Journal of Medicinal Chemistry|December 11, 2019
Discovery of a Covalent Inhibitor of KRAS<sup>G12C</sup> (AMG 510) for the Treatment of Solid TumorsBrian A Lanman, Jennifer R Allen, John G Allen, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
The Journal of Organic Chemistry|May 7, 2016
Telescoped Process to Manufacture 6,6,6-Trifluorofucose via Diastereoselective Transfer Hydrogenation: Scalable Access to an Inhibitor of Fucosylation Utilized in Monoclonal Antibody ProductionMichal M Achmatowicz, John G Allen, Matthew M Bio, et al.
Chemical Research in Toxicology|January 26, 2010
Cytochrome P450-mediated epoxidation of 2-aminothiazole-based AKT inhibitors: identification of novel GSH adducts and reduction of metabolic activation through structural changes guided by in silico and in vitro screeningRaju Subramanian, Matthew R Lee, John G Allen, et al.
Journal of Medicinal Chemistry|November 21, 2023
Imidazolone as an Amide Bioisostere in the Development of β-1,3-<i>N</i>-Acetylglucosaminyltransferase 2 (B3GNT2) InhibitorsJeffrey J Jackson, Aaron C Siegmund, Wen-Ju Bai, et al.
Bioorganic & Medicinal Chemistry Letters|October 15, 2013
The optimization of aminooxadiazoles as orally active inhibitors of Cdc7Paul E Harrington, Matthew P Bourbeau, Christopher Fotsch, et al.
ACS Chemical Biology|July 20, 2016
Facile Modulation of Antibody Fucosylation with Small Molecule Fucostatin Inhibitors and Cocrystal Structure with GDP-Mannose 4,6-DehydrataseJohn G Allen, Mirna Mujacic, Michael J Frohn, et al.
Journal of Medicinal Chemistry|October 28, 2009
Discovery and optimization of chromenotriazolopyrimidines as potent inhibitors of the mouse double minute 2-tumor protein 53 protein-protein interactionJohn G Allen, Matthew P Bourbeau, G Erich Wohlhieter, et al.
Bioorganic & Medicinal Chemistry Letters|February 9, 2010
Azole-based inhibitors of AKT/PKB for the treatment of cancerQingping Zeng, John G Allen, Matthew P Bourbeau, et al.
Journal of Medicinal Chemistry|July 14, 2026
Expanding Addressable KRAS Mutations through the Structure- and Property-Based Design of Dual-State (GDP/GTP), Reversible Pan-KRAS InhibitorsRyan P Wurz, Jennifer R Allen, John G Allen, et al.
Journal of Medicinal Chemistry|December 11, 2019
Discovery of a Covalent Inhibitor of KRAS<sup>G12C</sup> (AMG 510) for the Treatment of Solid TumorsBrian A Lanman, Jennifer R Allen, John G Allen, et al.
Pageof 2