KAJIAN STRUKTUR SENYAWA TURUNAN ASAM NAFTIL PROPIONAT SEBAGAI KANDIDAT  OBAT ANTIRADANG BUKAN STEROID

Please use this identifier to cite or link to this item: https://repository.unej.ac.id/xmlui/handle/123456789/58328

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DC Field	Value	Language
dc.contributor.author	Indah Purnama Sary	-
dc.date.accessioned	2014-07-14T06:20:12Z	-
dc.date.available	2014-07-14T06:20:12Z	-
dc.date.issued	2014-07-14	-
dc.identifier.uri	http://repository.unej.ac.id/handle/123456789/58328	-
dc.description.abstract	Anti-inflammatory activities of naphthyl propionic acid and its derivatives had been studied by molecular mechanics using ChemOffice® 2004 software. Results showed that anti-inflammatory activity of these compounds seem to be determined by a presence of sinister stereochemical configuration of the asymmetric centre of carbon 2 of substituted propionic acid, a presence of an acidic functional group at the carbon 2’ of naphthyl ring, a presence of a heteroatomic substituent having negative inductive effect at the carbon 6’ of naphthyl ring, and interatomic distance between heteroatom-bound H atom and naphthyl ring of 3.128 ± 0.575 Å with the optimum distance of 3.264 Å for naproxen.	en_US
dc.language.iso	other	en_US
dc.subject	study on structure, naphthyl propionic acid	en_US
dc.title	KAJIAN STRUKTUR SENYAWA TURUNAN ASAM NAFTIL PROPIONAT SEBAGAI KANDIDAT OBAT ANTIRADANG BUKAN STEROID	en_US
dc.type	Article	en_US
Appears in Collections:	Fakultas Farmasi

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