Alacepril
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(IUPAC) ime
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(2S)-2-([(2S)-1-[(2S)-3-acetilsulfanil-2-metilpropanoil]pirolidin-2-karbonil]amino)-3-fenilpropanoinska kiselina
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Klinički podaci
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AHFS/Drugs.com
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Internacionalno ime leka
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Identifikatori
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CAS broj
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74258-86-9
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ATC kod
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nije dodeljen
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PubChem[1][2]
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71992
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ChemSpider[3]
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64993
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UNII
|
X39TL7JDPF Y
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KEGG[4]
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D01900 Y
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Hemijski podaci
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Formula
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C20H26N2O5S
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Mol. masa
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406,49 g/mol
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SMILES
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eMolekuli & PubHem
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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 |
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Farmakoinformacioni podaci
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Trudnoća
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?
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Pravni status
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℞ Prescription only
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Način primene
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Oralno
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Alacepril je ACE inhibitor.[5]
- ↑ 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.