Tranilcipromin

Tranilcipromin
Klinički podaci
Prodajno imeDl-Tranylcypromine, Parnate, Transamine
Drugs.comMonografija
Način primeneOralno
Farmakokinetički podaci
Poluvreme eliminacije1,5-3,2 h
Identifikatori
CAS broj155-09-9 ДаY
ATC kodN06AF04 (WHO)
PubChemCID 441233
DrugBankDB00752 ДаY
ChemSpider390008 ДаY
KEGGC07155 ДаY
ChEMBLCHEMBL1179 ДаY
Hemijski podaci
FormulaC9H11N
Molarna masa133,190
  • N[C@@H]1CC1C1=CC=CC=C1
  • 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 ДаY
  • Key:AELCINSCMGFISI-YGPZHTELSA-N ДаY
Fizički podaci
Tačka topljenja79—80 °C (174—176 °F)

Tranilcipromin je organsko jedinjenje, koje sadrži 9 atoma ugljenika i ima molekulsku masu od 133,190 Da.[1][2][3][4]

Osobine

Osobina Vrednost
Broj akceptora vodonika 1
Broj donora vodonika 1
Broj rotacionih veza 1
Particioni koeficijent[5] (ALogP) 1,2
Rastvorljivost[6] (logS, log(mol/L)) -1,9
Polarna površina[7] (PSA, Å2) 26,0

Reference

  1. ^ Frieling H, Bleich S: Tranylcypromine: new perspectives on an old drug. Eur Arch Psychiatry Clin Neurosci. 2006 Aug;256(5):268-73. PMID 16927039
  2. ^ 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. PMID 14574774
  3. ^ 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. PMC 3013709Слободан приступ. PMID 21059682. doi:10.1093/nar/gkq1126. 
  4. ^ David S. Wishart; Craig Knox; An Chi Guo; Dean Cheng; Savita Shrivastava; Dan Tzur; Bijaya Gautam; Murtaza Hassanali (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. Nucleic acids research. 36 (Database issue): D901—6. PMC 2238889Слободан приступ. PMID 18048412. doi:10.1093/nar/gkm958. 
  5. ^ Ghose, A.K.; Viswanadhan V.N. & 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. 
  6. ^ 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. PMID 11749573. doi:10.1021/ci000392t. 
  7. ^ 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. PMID 11020286. doi:10.1021/jm000942e. 

Literatura

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