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Chemical Science|June 14, 2021
Fluorogenic Trp(redBODIPY) cyclopeptide targeting keratin 1 for imaging of aggressive carcinomasRamon Subiros-Funosas, Vivian Cheuk Lam Ho, Nicole D Barth, et al.
Nature Communications|May 21, 2021
Structural insights on ligand recognition at the human leukotriene B4 receptor 1Nairie Michaelian, Anastasiia Sadybekov, Élie Besserer-Offroy, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|August 20, 2025
Discovering Uncharted Binding Pockets on E3 Ligases Leads to the Identification of FBW7 Allosteric ModulatorsMíriam Martínez-Cartró, Álvaro Serrano-Morrás, Andrea Bertran-Mostazo, et al.
Bioorganic & Medicinal Chemistry Letters|August 17, 2019
Design of selective PI3Kδ inhibitors using an iterative scaffold-hopping workflowXavier Fradera, Joey L Methot, Abdelghani Achab, et al.
Antibiotics (Basel, Switzerland)|May 28, 2022
Computational Design of Inhibitors Targeting the Catalytic β Subunit of <i>Escherichia coli</i> F<sub>O</sub>F<sub>1</sub>-ATP SynthaseLuis Pablo Avila-Barrientos, Luis Fernando Cofas-Vargas, Guillermin Agüero-Chapin, et al.
Chemistry & Biology|June 26, 2004
Structure-activity relationships in purine-based inhibitor binding to HSP90 isoformsLisa Wright, Xavier Barril, Brian Dymock, et al.
ACS Medicinal Chemistry Letters|March 19, 2021
Identification of Potent Reverse Indazole Inhibitors for HPK1Elsie C Yu, Joey L Methot, Xavier Fradera, et al.
Bioorganic & Medicinal Chemistry Letters|August 15, 2021
Discovery of IDO1 inhibitors containing a decahydroquinoline, decahydro-1,6-naphthyridine, or octahydro-1H-pyrrolo[3,2-c]pyridine scaffoldWensheng Yu, Yongqi Deng, David Sloman, et al.
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