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Structural similarities can be seen between daclatasvir and the more recent inhibitors as shown in blue. Daclatasvir was developed by Bristol-Myers Squibb, ledipasvir by Gilead Sciences, ombitasvir by AbbVie Inc.

E. Aprile, J. Aalbers, F. Agostini, M. Alfonsi, L. Althueser, F. D. Amaro, M. Anthony, V. C. Antochi, F. Arneodo, L. Baudis, B. Bauermeister, M. L. Benabderrahmane, T. Berger, P. A. Cushman Publications 1. M. Cushman and N. Castagnoli, Jr., "The Condensation of Schiff Bases with Succinic Anhydrides. Scope and Mechanism," J. Org. Chem., 36, 3404 (1971). 2. M. Cushman and N. Structural similarities can be seen between daclatasvir and the more recent inhibitors as shown in blue. Daclatasvir was developed by Bristol-Myers Squibb, ledipasvir by Gilead Sciences, ombitasvir by AbbVie Inc. Which of these processes occurs depends on the genus. Among starfish that are able to regenerate their whole body from a single arm, some can do so even from fragments just 1 cm (0.4 in) long. Single arms that regenerate a whole individual… A boronic acid is a compound related to boric acid in which one of the three hydroxyl groups is replaced by an alkyl or aryl group. As a compound containing a carbon–boron bond, members of this class thus belong to the larger class of… Frank Henry Westheimer (January 15, 1912 – April 14, 2007) was an American chemist. He taught at the University of Chicago from 1936 to 1954, and at Harvard University from 1953 to 1983, becoming the Morris Loeb Professor of Chemistry in… Diphenoxylate is a centrally active opioid drug of the phenylpiperidine series that is used in a combination drug with atropine for the treatment of diarrhea.