Cite
Discovery of (R)-N-(3-(7-methyl-1H-indazol-5-yl)-1-(4-(1-methylpiperidin-4-yl)-1-oxopropan-2-yl)-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide (BMS-742413): A potent human CGRP antagonist with superior safety profile for the treatment of migraine through intranasal delivery
MLA
John E. Macor, et al. “Discovery of (R)-N-(3-(7-Methyl-1H-Indazol-5-Yl)-1-(4-(1-Methylpiperidin-4-Yl)-1-Oxopropan-2-Yl)-4-(2-Oxo-1,2-Dihydroquinolin-3-Yl)Piperidine-1-Carboxamide (BMS-742413): A Potent Human CGRP Antagonist with Superior Safety Profile for the Treatment of Migraine through Intranasal Delivery.” Bioorganic & Medicinal Chemistry Letters, vol. 23, June 2013, pp. 3157–61. EBSCOhost, https://doi.org/10.1016/j.bmcl.2013.04.012.
APA
John E. Macor, Chaturvedula Prasad, Rex Denton, Gene M. Dubowchik, Paul Moench, Valerie J. Whiterock, Charlie M. Conway, Cen Xu, Neil Mathias, Glenn H. Cantor, Robert Macci, Richard Schartman, Laura J. Signor, Stephen E. Mercer, George Thalody, Carl D. Davis, Deborah Keavy, & Sokhom S. Pin. (2013). Discovery of (R)-N-(3-(7-methyl-1H-indazol-5-yl)-1-(4-(1-methylpiperidin-4-yl)-1-oxopropan-2-yl)-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide (BMS-742413): A potent human CGRP antagonist with superior safety profile for the treatment of migraine through intranasal delivery. Bioorganic & Medicinal Chemistry Letters, 23, 3157–3161. https://doi.org/10.1016/j.bmcl.2013.04.012
Chicago
John E. Macor, Chaturvedula Prasad, Rex Denton, Gene M. Dubowchik, Paul Moench, Valerie J. Whiterock, Charlie M. Conway, et al. 2013. “Discovery of (R)-N-(3-(7-Methyl-1H-Indazol-5-Yl)-1-(4-(1-Methylpiperidin-4-Yl)-1-Oxopropan-2-Yl)-4-(2-Oxo-1,2-Dihydroquinolin-3-Yl)Piperidine-1-Carboxamide (BMS-742413): A Potent Human CGRP Antagonist with Superior Safety Profile for the Treatment of Migraine through Intranasal Delivery.” Bioorganic & Medicinal Chemistry Letters 23 (June): 3157–61. doi:10.1016/j.bmcl.2013.04.012.