Kvinapril

Kvinapril
(IUPAC) ime
	(3S)-2-[(2S)-2- {[(2S)-1-etoksi-1-okso-4-fenilbutan-2-il]amino}propanoil]-1,2,3,4-tetrahidroizohinolin-3-karboksilna kiselina
Klinički podaci
Robne marke	Accupril
AHFS/Drugs.com	Monografija
MedlinePlus	a692026
Identifikatori
CAS broj	85441-61-8
ATC kod	C09AA06
PubChem	54892
DrugBank	DB00881
ChemSpider	49565
UNII	RJ84Y44811
KEGG	D03752
ChEBI	CHEBI:8713
ChEMBL	CHEMBL1592
Hemijski podaci
Formula	C25H30N2O5
Mol. masa	438,516 g/mol
SMILES	eMolekuli & PubHem
InChI
	InChI=1S/C25H30N2O5/c1-3-32-25(31)21(14-13-18-9-5-4-6-10-18)26-17(2)23(28)27-16-20-12-8-7-11-19(20)15-22(27)24(29)30/h4-12,17,21-22,26H,3,13-16H2,1-2H3,(H,29,30)/t17-,21-,22-/m0/s1 ; Key: JSDRRTOADPPCHY-HSQYWUDLSA-N
Farmakokinetički podaci
Vezivanje za proteine plazme	97%
Poluvreme eliminacije	2 sata
Farmakoinformacioni podaci
Trudnoća	?
Pravni status	℞ Prescription only
Način primene	Oralno

Kvinapril (Accupril) je inhibitor angiotenzin konvertujućeg enzima (ACE inhibitor) koji se koristi u tretmanu hipertenzije i zatajenja srca.

Farmakologija

Kvinapril je prolek. On se konvertuje u aktivni metabolit, kvinaprilat, u jetri.^[6]

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ Keith Parker; Laurence Brunton; Goodman, Louis Sanford; Lazo, John S.; Gilman, Alfred (2006). Goodman & Gilman's The Pharmacological Basis of Therapeutics (11 izd.). New York: McGraw-Hill. ISBN 0-07-142280-3.

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