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Localization of dipyridamole molecules in ionic micelles: effect of micelle and drug charges

โœ Scribed by Iouri E. Borissevitch; Christiane P.F. Borges; Victor E. Yushmanov; Marcel Tabak

Book ID
115731018
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
554 KB
Volume
1238
Category
Article
ISSN
0005-2736

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Synthesis, characterization and interact
Synthesis, characterization and interaction with ionic micelles of tetraacetylated dipyridamole
โœ Christiane P.F Borges; Shinya Honda; Roberto G.S Berlinck; Hidetake Imasato; Ped ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 532 KB

Tetraacetylated dipyridamole (Ac-DIP) was synthesized by reaction of dipyridamole (DIP) with acetic anhydride in a quantitative yield. Infrared and NMR spectra showed that the acetylation was complete, yielding the expected new bands and the disappearance of hydroxyl bands in the IR and NMR spectra.