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Journal of Medicinal Chemistry|February 7, 2015
Engineering potent and selective analogues of GpTx-1, a tarantula venom peptide antagonist of the Na(V)1.7 sodium channelJustin K Murray, Joseph Ligutti, Dong Liu, et al.
The Journal of Biological Chemistry|June 26, 2009
Hepcidin revisited, disulfide connectivity, dynamics, and structureJohn B Jordan, Leszek Poppe, Mitsuru Haniu, et al.
Bioorganic & Medicinal Chemistry Letters|June 27, 2015
Sustained inhibition of the NaV1.7 sodium channel by engineered dimers of the domain II binding peptide GpTx-1Justin K Murray, Kaustav Biswas, J Ryan Holder, et al.
Journal of Medicinal Chemistry|April 17, 2008
Design and synthesis of conformationally constrained glucagon-like peptide-1 derivatives with increased plasma stability and prolonged in vivo activityLes P Miranda, Katherine A Winters, Colin V Gegg, et al.
Journal of Medicinal Chemistry|March 14, 2022
Targeting the Mitotic Kinesin KIF18A in Chromosomally Unstable Cancers: Hit Optimization Toward an In Vivo Chemical ProbeNuria A Tamayo, Matthew P Bourbeau, Jennifer R Allen, et al.
Cancer Discovery|September 27, 2018
AMG 176, a Selective MCL1 Inhibitor, Is Effective in Hematologic Cancer Models Alone and in Combination with Established TherapiesSean Caenepeel, Sean P Brown, Brian Belmontes, 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.
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