Download presentation
Presentation is loading. Please wait.
1
Chemical structure of eteplirsen (Drugbank Accession Number: DB06014);43 IUPAC chemical name: (P-deoxy-P-(dimethylamino)](2',3'-dideoxy-2',3'-imino-2',3'-seco)(2'a→5')(C-m5U-C-C-A-A-C-A-m5U-C-A-A-G-G-A-A-G-A-m5U-G-G-C-A-m5U-m5U-m5U-C-m5U-A-G),5'-(P-(4-((2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)carbonyl)-1-piperazinyl)-N,N-dimethylphosphonamidate) RNA Source: The Goodman & Gilman Year in Review: New and Noteworthy FDA Approvals, Goodman & Gilman's: The Pharmacological Basis of Therapeutics, 12e Citation: Brunton LL, Chabner BA, Knollmann BC. Goodman & Gilman's: The Pharmacological Basis of Therapeutics, 12e; 2011 Available at: Accessed: November 11, 2017 Copyright © 2017 McGraw-Hill Education. All rights reserved
(2 a→5 )(C-m5U-C-C-A-A-C-A-m5U-C-A-A-G-G-A-A-G-A-m5U-G-G-C-A-m5U-m5U-m5U-C-m5U-A-G),5 -(P-(4-((2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)carbonyl)-1-piperazinyl)-N,N-dimethylphosphonamidate) RNA](http://slideplayer.com/slide/13562853/82/images/1/Chemical+structure+of+eteplirsen+%28Drugbank+Accession+Number%3A+DB06014%29%3B43+IUPAC+chemical+name%3A+%28P-deoxy-P-%28dimethylamino%29%5D%282+%2C3+-dideoxy-2+%2C3+-imino-2+%2C3+-seco%29%282+a%E2%86%925+%29%28C-m5U-C-C-A-A-C-A-m5U-C-A-A-G-G-A-A-G-A-m5U-G-G-C-A-m5U-m5U-m5U-C-m5U-A-G%29%2C5+-%28P-%284-%28%282-%282-%282-hydroxyethoxy%29ethoxy%29ethoxy%29carbonyl%29-1-piperazinyl%29-N%2CN-dimethylphosphonamidate%29+RNA.jpg "Source: The Goodman & Gilman Year in Review: New and Noteworthy FDA Approvals, Goodman & Gilman s: The Pharmacological Basis of Therapeutics, 12e. Citation: Brunton LL, Chabner BA, Knollmann BC. Goodman & Gilman s: The Pharmacological Basis of Therapeutics, 12e; 2011 Available at: image=/data/books/1613/bru12_ch2016pt1_f001.png&sec= &BookID=1613&ChapterSecID= &imagename= Accessed: November 11, Copyright © 2017 McGraw-Hill Education. All rights reserved.")
Similar presentations
