Levobupivakain

Levobupivakain
Klinički podaci
Drugs.comMonografija
Način primeneParenteralno
Farmakokinetički podaci
Poluvreme eliminacije3,3 h
IzlučivanjeRenalno (95%)
Identifikatori
CAS broj27262-47-1 ДаY
ATC kodN01BB10 (WHO)
PubChemCID 92253
DrugBankDB01002 ДаY
ChemSpider83289 ДаY
KEGGC07887 ДаY
ChEBICHEBI:6149 ДаY
ChEMBLCHEMBL1201193 ДаY
Hemijski podaci
FormulaC18H28N2O
Molarna masa288,428
  • CCCCN1CCCC[C@H]1C(=O)NC1=C(C)C=CC=C1C
  • InChI=1S/C18H28N2O/c1-4-5-12-20-13-7-6-11-16(20)18(21)19-17-14(2)9-8-10-15(17)3/h8-10,16H,4-7,11-13H2,1-3H3,(H,19,21)/t16-/m0/s1 ДаY
  • Key:LEBVLXFERQHONN-INIZCTEOSA-N ДаY

Levobupivakain je organsko jedinjenje, koje sadrži 18 atoma ugljenika i ima molekulsku masu od 288,428 Da.[1][2][3][4]

Osobine

Osobina Vrednost
Broj akceptora vodonika 2
Broj donora vodonika 1
Broj rotacionih veza 5
Particioni koeficijent[5] (ALogP) 4,3
Rastvorljivost[6] (logS, log(mol/L)) -4,6
Polarna površina[7] (PSA, Å2) 32,3

Reference

  1. ^ Leone S, Di Cianni S, Casati A, Fanelli G: Pharmacology, toxicology, and clinical use of new long acting local anesthetics, ropivacaine and levobupivacaine. Acta Biomed. 2008 Aug;79(2):92-105. PMID 18788503 18788503
  2. ^ Burlacu CL, Buggy DJ: Update on local anesthetics: focus on levobupivacaine. Ther Clin Risk Manag. 2008 Apr;4(2):381-92. PMID 18728849
  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.  уреди
  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.  уреди
  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.  уреди
  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.  уреди

Literatura

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