Alacepril je ACE inhibitor.[5]
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
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| Identifikatori
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| CAS broj
|
74258-86-9
|
| ATC kod
|
nije dodeljen
|
| PubChem[1][2]
|
71992
|
| ChemSpider[3]
|
64993
|
| UNII
|
X39TL7JDPF  Y
|
| KEGG[4]
|
D01900 Y
|
| 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 Y
Key: FHHHOYXPRDYHEZ-COXVUDFISA-N Y |
|
| Farmakoinformacioni podaci
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| Trudnoća
|
?
|
| Pravni status
|
℞ Prescription only
|
| Način primene
|
Oralno
|
- ↑ 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.
- ↑ Toshio Ogihara1, Yoshihiro Tachi, Hitoshi Uno (1992). Alacepril. 10. pp. 88–100. DOI:10.1111/j.1527-3466.1992.tb00238.x.
