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Bioorganic & Medicinal Chemistry|April 3, 2014
α-Ketoheterocycle inhibitors of fatty acid amide hydrolase: exploration of conformational constraints in the acyl side chainKatharine K Duncan, Katerina Otrubova, Dale L BogerACS Medicinal Chemistry Letters|January 17, 2012
10'-Fluorovinblastine and 10'-Fluorovincristine: Synthesis of a Key Series of Modified Vinca AlkaloidsHiroaki Gotoh, Katharine K Duncan, William M Robertson, et al.ACS Medicinal Chemistry Letters|November 14, 2013
Potent Vinblastine C20' Ureas Displaying Additionally Improved Activity Against a Vinblastine-Resistant Cancer Cell LineTimothy J Barker, Katharine K Duncan, Katerina Otrubova, et al.Frontiers in Robotics and AI|January 27, 2021
Exploring Novel Biologically-Relevant Chemical Space Through Artificial Intelligence: The NCATS ASPIRE ProgramKatharine K Duncan, Dobrila D Rudnicki, Christopher P Austin, et al.Organic Letters|February 29, 2012
Iron(III)/NaBH4-mediated additions to unactivated alkenes: synthesis of novel 20'-vinblastine analoguesErick K Leggans, Timothy J Barker, Katharine K Duncan, et al.Organic Letters|October 4, 2013
Transannular Diels-Alder/1,3-dipolar cycloaddition cascade of 1,3,4-oxadiazoles: total synthesis of a unique set of vinblastine analoguesErica L Campbell, Colin K Skepper, Kuppusamy Sankar, et al.The Journal of Chemical Physics|July 21, 2004
Nuclear quadrupole hyperfine structure in the microwave spectrum of HCl-N2O: electric field gradient perturbation of N2O by HClHelen O Leung, Winn T Cashion, Katharine K Duncan, et al.Journal of Medicinal Chemistry|December 19, 2012
A remarkable series of vinblastine analogues displaying enhanced activity and an unprecedented tubulin binding steric tolerance: C20' urea derivativesErick K Leggans, Katharine K Duncan, Timothy J Barker, et al.Journal of Medicinal Chemistry|December 21, 2012
Total synthesis and evaluation of vinblastine analogues containing systematic deep-seated modifications in the vindoline subunit ring system: core redesignKristin D Schleicher, Yoshikazu Sasaki, Annie Tam, et al.Journal of Medicinal Chemistry|August 16, 2013
A fundamental relationship between hydrophobic properties and biological activity for the duocarmycin class of DNA-alkylating antitumor drugs: hydrophobic-binding-driven bondingAmanda L Wolfe, Katharine K Duncan, James P Lajiness, et al.Pageof 2