Iproniazid
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(IUPAC) ime | |||
---|---|---|---|
N'-izopropilizonikotinohidrazid | |||
Klinički podaci | |||
AHFS/Drugs.com | Internacionalno ime leka | ||
Identifikatori | |||
CAS broj | 54-92-2 | ||
ATC kod | N06AF05 | ||
PubChem[1][2] | 3748 | ||
DrugBank | DB04818 | ||
ChemSpider[3] | 3617 | ||
UNII | D892HFI3XA ![]() | ||
KEGG[4] | D02579 ![]() | ||
ChEMBL[5] | CHEMBL92401 ![]() | ||
Hemijski podaci | |||
Formula | C9H13N3O | ||
Mol. masa | 179,219 | ||
SMILES | eMolekuli & PubHem | ||
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Farmakokinetički podaci | |||
Bioraspoloživost | ? | ||
Metabolizam | ? | ||
Poluvreme eliminacije | ? | ||
Izlučivanje | ? | ||
Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status | ? | ||
Način primene | ? |
Iproniazid (Eufozid, Iprazid, Ipronid, Ipronin, Marsilid, Rivivol) je hidrazinski lek koji je korišten kao antidepresiv.[6] On deluje kao ireverzibilni i neselektivni inhibitor monoaminske oksidaze (MAOI).[7]
Reference[uredi - уреди | uredi izvor]
- ↑ 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003.
- ↑ 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. PMID 20331846. doi:10.1186/1758-2946-2-3.
- ↑ 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. PMID 21948594. doi:10.1093/nar/gkr777.
- ↑ Robert A. Maxwell, Shohreh B. Eckhardt (1990). Drug discovery. Humana Press. str. 143–154. ISBN 0-89603-180-2, 9780896031807.
- ↑ Fagervall I, Ross SB (April 1986). "Inhibition of monoamine oxidase in monoaminergic neurones in the rat brain by irreversible inhibitors". Biochemical pharmacology 35 (8): 1381–7. PMID 2870717. doi:10.1016/0006-2952(86)90285-6.
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