Alacepril

Alacepril
(IUPAC) ime
(2S)-2-([(2S)-1-[(2S)-3-acetilsulfanil-2-metilpropanoil]pirolidin-2-karbonil]amino)-3-fenilpropanoinska kiselina
Klinički podaci
AHFS/Drugs.com Internacionalno ime leka
Identifikatori
CAS broj 74258-86-9
ATC kod nije dodeljen
PubChem[1][2] 71992
ChemSpider[3] 64993
UNII X39TL7JDPF DaY
KEGG[4] D01900 DaY
Hemijski podaci
Formula C20H26N2O5S 
Mol. masa 406,49 g/mol
SMILES eMolekuli & PubHem
InChI
InChI=1S/C20H26N2O5S/c1-13(12-28-14(2)23)19(25)22-10-6-9-17(22)18(24)21-16(20(26)27)11-15-7-4-3-5-8-15/h3-5,7-8,13,16-17H,6,9-12H2,1-2H3,(H,21,24)(H,26,27)/t13-,16+,17+/m1/s1 DaY
Key: FHHHOYXPRDYHEZ-COXVUDFISA-N DaY
Farmakoinformacioni podaci
Trudnoća ?
Pravni status Prescription only
Način primene Oralno

Alacepril je ACE inhibitor.[5]

Reference

  1. 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
  2. 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. 
  3. 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
  4. 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. 
  5. Toshio Ogihara1, Yoshihiro Tachi, Hitoshi Uno (1992). Alacepril. 10. pp. 88–100. DOI:10.1111/j.1527-3466.1992.tb00238.x. 
  • p
  • r
  • u
Antihipertenzivi: Lekovi koji deluju na renin-angiotenzin sistem (C09)
AKE inhibitori/
("-pril")AIIRAi/
("-sartan")Renin inhibitori/
("-kiren")

M: VAS

anat (a:h/u/t/a/l,v:h/u/t/a/l)/phys/devp/cell/prot

vabo/siva/kong/tumr, sizn/epon

proc, lek (C2s+n/3/4/5/7/8/9)