Flumazenil
Изглед
Klinički podaci | |
---|---|
Prodajno ime | Anexate, Flumazepil, Lanexat, Mazicon |
Drugs.com | Monografija |
Način primene | Intravenozno |
Farmakokinetičkipodaci | |
Poluvreme eliminacije | 4 - 11 minuta |
Izlučivanje | Renalno |
Identifikatori | |
CAS broj | 78755-81-4 |
ATC kod | V03AB25(WHO) |
PubChem | CID3373 |
DrugBank | DB01205 |
ChemSpider | 3256 |
KEGG | C07825 |
ChEBI | CHEBI:5103 |
ChEMBL | CHEMBL407 |
Hemijski podaci | |
Formula | C15H14FN3O3 |
Molarna masa | 303,288 |
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Fizički podaci | |
Tačka topljenja | 201—203 °C (394—397 °F) |
Flumazeniljeorgansko jedinjenje,koje sadrži 15atomaugljenikai imamolekulsku masuod 303,288Da.[1][2][3][4][5]
Osobine
[уреди|уреди извор]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 |
Reference
[уреди|уреди извор]- ^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
- ^Olkkola KT, Ahonen J: Midazolam and other benzodiazepines. Handb Exp Pharmacol. 2008;(182):335-60.PMID18175099
- ^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
- ^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.PMC3013709 .PMID21059682.doi:10.1093/nar/gkq1126.
- ^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.PMC2238889 .PMID18048412.doi:10.1093/nar/gkm958.
- ^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.
- ^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.
- ^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.
Literatura
[уреди|уреди извор]- Hardman JG, Limbird LE, Gilman AG (2001).Goodman & Gilman's The Pharmacological Basis of Therapeutics(10. изд.). New York: McGraw-Hill.ISBN0071354697.doi:10.1036/0071422803.
- Thomas L. Lemke; David A. Williams, ур. (2007).Foye's Principles of Medicinal Chemistry(6. изд.). Baltimore: Lippincott Willams & Wilkins.ISBN0781768799.
Spoljašnje veze
[уреди|уреди извор]
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