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Flumazenil

С Википедије, слободне енциклопедије
Flumazenil
Klinički podaci
Prodajno imeAnexate, Flumazepil, Lanexat, Mazicon
Drugs.comMonografija
Način primeneIntravenozno
Farmakokinetičkipodaci
Poluvreme eliminacije4 - 11 minuta
IzlučivanjeRenalno
Identifikatori
CAS broj78755-81-4ДаY
ATC kodV03AB25(WHO)
PubChemCID3373
DrugBankDB01205ДаY
ChemSpider3256ДаY
KEGGC07825ДаY
ChEBICHEBI:5103ДаY
ChEMBLCHEMBL407ДаY
Hemijski podaci
FormulaC15H14FN3O3
Molarna masa303,288
  • CCOC(=O)C1=C2CN(C)C(=O)C3=C(C=CC(F)=C3)N2C=N1
  • InChI=1S/C15H14FN3O3/c1-3-22-15(21)13-12-7-18(2)14(20)10-6-9(16)4-5-11(10)19(12)8-17-13/h4-6,8H,3,7H2,1-2H3ДаY
  • Key:OFBIFZUFASYYRE-UHFFFAOYSA-NДаY
Fizički podaci
Tačka topljenja201—203 °C (394—397 °F)

Flumazeniljeorgansko jedinjenje,koje sadrži 15atomaugljenikai imamolekulsku masuod 303,288Da.[1][2][3][4][5]

Osobina Vrednost
Broj akceptora vodonika 4
Broj donora vodonika 0
Broj rotacionih veza 3
Particioni koeficijent[6](ALogP) 1,6
Rastvorljivost[7](logS,log(mol/L)) -3,0
Polarna površina[8](PSA,Å2) 64,4
  1. ^Ngo AS, Anthony CR, Samuel M, Wong E, Ponampalam R: Should a benzodiazepine antagonist be used in unconscious patients presenting to the emergency department? Resuscitation. 2007 Jul;74(1):27-37. Epub 2007 Feb 15.PMID17306436
  2. ^Olkkola KT, Ahonen J: Midazolam and other benzodiazepines. Handb Exp Pharmacol. 2008;(182):335-60.PMID18175099
  3. ^Maeda S, Miyawaki T, Higuchi H, Shimada M: Effect of flumazenil on disturbance of equilibrium function induced by midazolam. Anesth Prog. 2008 Fall;55(3):73-7.PMID18788841
  4. ^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.PMC3013709Слободан приступ.PMID21059682.doi:10.1093/nar/gkq1126.уреди
  5. ^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.PMC2238889Слободан приступ.PMID18048412.doi:10.1093/nar/gkm958.уреди
  6. ^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.
  7. ^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.PMID11749573.doi:10.1021/ci000392t.уреди
  8. ^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.PMID11020286.doi:10.1021/jm000942e.уреди


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