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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2010
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/20319
Title: | Application of the NMR spectroscopy in the structural analysis of clonidine |
Authors: | Lisnic, Alexandru Palii, Vasile |
Issue Date: | 2010 |
Publisher: | Nicolae Testemitanu State Medical and Pharmaceutical University |
Citation: | LISNIC, Alexandru, PALII, Vasile. Application of the NMR spectroscopy in the structural analysis of clonidine. In: MedEspera: the 3rd Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2010, p. 101. |
Abstract: | NMR spectroscopy is one of the most powerful techniques available for studying the
structure of molecules. It involves the absorption of radioawaves by the nuclei of some combined
atoms (: 1H, 13C, 15N, 19F, 3 IP) in a molecule that is located in a magnetic field. Nuclear magnetic
resonance spectroscopy is the use of the NMR phenomenon to study physical, chemical, and
biological properties of matter. The most important applications are proton NMR and carbon-13
NMR spectroscopy. In principle, NMR is applicable to any nucleus possessing spin. This property of
nucleis to have a spin, was used to establish the structure of clonidine using 1H and 13C spectrum.
Clonidine-N-(2,6-dichlorophenyl)-4,5-dihydro-lH-imidazol-2-amine- treats high blood pressure by
stimulating ?2 receptors in the brain, which decreases cardiac output and peripheral vascular
resistance, lowering blood pressure. It has specificity towards thepresynaptic ?2 receptors in the
vasomotor center in the brainstem. This binding decreases presynaptic calcium levels, and inhibits the
release of norepinephrine (NE). The net effect is a decrease in sympathetic tone. Was determinated : •
the number of carbon atoms using 13C spectrum(DMSO), and their shift's, ppm : 158.5(C7),
134.5(C8), 129.7(C9), 131.5(C10), 129.7(C11), 130.5(C12). • the number of hydrogen atoms using
1H spectrum(DMSO), and thei shift's, ppm : 7.58(H9), 7.46(H10), 7.58(H11), 10.72(H6), 8.5ЦН1),
43.2(2H4d, 2H5d). The obtained spectrum gave us the possibility to establish the spatial structure of
the analyzed sample. The impact of NMR spectroscopy on the natural sciences has been substantial. It
can, among other things, be used to study mixtures of analytes, to understand dynamic effects such as
change in temperature and reaction mechanisms, and is an invaluable tool in understanding protein
and nucleic acid structure and function. It can be applied to a wide variety of samples, both in the
solution and the solid state. |
metadata.dc.relation.ispartof: | MedEspera: The 3rd International Medical Congress for Students and Young Doctors, May 19-21, 2010, Chisinau, Republic of Moldova |
URI: | http://repository.usmf.md/handle/20.500.12710/20319 |
Appears in Collections: | MedEspera 2010
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