CONFORMATIONAL STUDY OF TAURINE AND ITS DERIVATIVES

Citation
D. Braghiroli et M. Dibella, CONFORMATIONAL STUDY OF TAURINE AND ITS DERIVATIVES, Il Farmaco, 50(7-8), 1995, pp. 555-557
Citations number
8
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
0014827X
Volume
50
Issue
7-8
Year of publication
1995
Pages
555 - 557
Database
ISI
SICI code
0014-827X(1995)50:7-8<555:CSOTAI>2.0.ZU;2-4
Abstract
In order to study the conformations of taurine in solution, H-1 NMR sp ectra of taurine, taurocyamine and their methylderivatives were record ed at different temperature and pH values. H-1 NMR spectra showed that the rotation around the C-C single bonds is usually in part hindered at room temperature and pH 7, and increases at higher temperature or a t acidic pH values. At alkaline pH values the rotational mobility seem s to be hindered. Only in taurocyamine molecule the rotation around th e C-C bond appears mostly free.