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Tranilcipromin

Izvor: Wikipedija
Tranilcipromin
Klinički podaci
Robne markeDl-Tranylcypromine, Parnate, Transamine
AHFS/Drugs.comMonografija
Identifikatori
CAS broj155-09-9
ATC kodN06AF04
PubChem[1][2]441233
DrugBankDB00752
ChemSpider[3]390008
KEGG[4]C07155 DaY
ChEMBL[5]CHEMBL1179 DaY
Hemijski podaci
FormulaC9H11N 
Mol. masa133,190
SMILESeMolekuli &PubHem
InChI
InChI=1S/C9H11N/c10-9-6-8(9)7-4-2-1-3-5-7/h1-5,8-9H,6,10H2/t8?,9-/m1/s1
Key: AELCINSCMGFISI-YGPZHTELSA-N DaY
Fizički podaci
Tačka topljenja79-80 °C (-33 °F)
Farmakokinetički podaci
Poluvreme eliminacije1,5-3,2 h
Farmakoinformacioni podaci
Trudnoća?
Pravni status
Način primeneOralno

Tranilcipromin jeorgansko jedinjenje, koje sadrži 9atomaugljenika i imamolekulsku masu od 133,190Da.[6][7][8][9]

Osobine

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OsobinaVrednost
Broj akceptora vodonika1
Broj donora vodonika1
Broj rotacionih veza1
Particioni koeficijent[10] (ALogP)1,2
Rastvorljivost[11] (logS, log(mol/L))-1,9
Polarna površina[12] (PSA,Å2)26,0

Reference

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  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. 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
  6. Frieling H, Bleich S: Tranylcypromine: new perspectives on an old drug. Eur Arch Psychiatry Clin Neurosci. 2006 Aug;256(5):268-73.PMID16927039
  7. Nolen WA: [Classical monoamine oxidase inhibitor: not registered for, but still a place in the treatment of depression] Ned Tijdschr Geneeskd. 2003 Oct 4;147(40):1940-3.PMID14574774
  8. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS (2011). „DrugBank 3.0: a comprehensive resource for omics research on drugs”. Nucleic Acids Res. 39 (Database issue): D1035-41. DOI:10.1093/nar/gkq1126. PMC 3013709. PMID 21059682. 
  9. David S. Wishart, Craig Knox, An Chi Guo, Dean Cheng, Savita Shrivastava, Dan Tzur, Bijaya Gautam, and Murtaza Hassanali (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Res 36 (Database issue): D901-6. DOI:10.1093/nar/gkm958. PMC 2238889. PMID 18048412. 
  10. Ghose, A.K., Viswanadhan V.N., and Wendoloski, J.J. (1998). „Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragment Methods: An Analysis of AlogP and CLogP Methods”. J. Phys. Chem. A 102: 3762-3772. DOI:10.1021/jp980230o. 
  11. Tetko IV, Tanchuk VY, Kasheva TN, Villa AE. (2001). „Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”. Chem Inf. Comput. Sci. 41: 1488-1493. DOI:10.1021/ci000392t. PMID 11749573. 
  12. Ertl P., Rohde B., Selzer P. (2000). „Fast calculation of molecular polar surface area as a sum of fragment based contributions and its application to the prediction of drug transport properties”. J. Med. Chem. 43: 3714-3717. DOI:10.1021/jm000942e. PMID 11020286. 

Literatura

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Vanjske veze

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Portal Medicina
Portal Hemija
Tranilcipromin naWikimedijinoj ostavi
Izvor:https://sh.wikipedia.org/w/index.php?title=Tranilcipromin&oldid=42290420
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