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Journal of Medicinal Chemistry|May 26, 2023
Discovery of 2-(Anilino)pyrimidine-4-carboxamides as Highly Potent, Selective, and Orally Active Glycogen Synthase Kinase-3 (GSK-3) InhibitorsRichard A Hartz, Vijay T Ahuja, Guanglin Luo, et al.Bioorganic & Medicinal Chemistry Letters|October 23, 2020
Azepino-indazoles as calcitonin gene-related peptide (CGRP) receptor antagonistsStephen E Mercer, Prasad V Chaturvedula, Charles M Conway, et al.Bioorganic & Medicinal Chemistry Letters|February 14, 2013
The synthesis and SAR of calcitonin gene-related peptide (CGRP) receptor antagonists derived from tyrosine surrogates. Part 2Xiaojun Han, Rita L Civiello, Charles M Conway, et al.Journal of Medicinal Chemistry|July 31, 2008
Discovery of (R)-4-(8-fluoro-2-oxo-1,2-dihydroquinazolin-3(4H)-yl)-N-(3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-(4-(piperidin-1-yl)piperidin-1-yl)propan-2-yl)piperidine-1-carboxamide (BMS-694153): a potent antagonist of the human calcitonin gene-related peptide receptor for migraine with rapid and efficient intranasal exposureAndrew P Degnan, Prasad V Chaturvedula, Charles M Conway, et al.Bioorganic & Medicinal Chemistry Letters|April 8, 2015
Discovery of new acylaminopyridines as GSK-3 inhibitors by a structure guided in-depth exploration of chemical space around a pyrrolopyridinone corePrasanna Sivaprakasam, Xiaojun Han, Rita L Civiello, et al.Pageof 5