Description
Flumazenil is an antagonist at GABA-A receptors that is used as a stimulant to counteract the effects of benzodiazepines. Flumenazil inhibits benzodiazepine-induced sedation, motor impairment, and ventilator depression.
| Product Unit Size | Cost | Quantity | Stock |
|---|
Flumazenil is an antagonist at GABA-A receptors that is used as a stimulant to counteract the effects of benzodiazepines. Flumenazil inhibits benzodiazepine-induced sedation, motor impairment, and ventilator depression.
| Cas No. | 78755-81-4 |
|---|---|
| Purity | ≥98% |
| Formula | C15H14FN3O3 |
| Formula Wt. | 303.29 |
| Chemical Name | 8-Fluoro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepinne-3-carboxylic acid ethyl ester |
| IUPAC Name | ethyl 8-fluoro-5-methyl-6-oxo-4H-imidazo[1,5-a][1, 4]benzodiazepine-3-carboxylate |
| Synonym | Anexate, Ro-15-1788, Lanexat, Romazicon |
| Melting Point | 201-203°C |
| Solubility | Soluble in water (128mg/L). |
| Appearance | A white or almost white crystalline powder |
| Store Temp | 4°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Rye DB, Bliwise DL, Parker K, et al. Modulation of vigilance in the primary hypersomnias by endogenous enhancement of GABAA receptors. Sci Transl Med. 2012 Nov 21;4(161):161ra151. PMID: 23175709.
Lader M. Benzodiazepines revisited--will we ever learn? Addiction. 2011 Dec;106(12):2086-109. PMID: 21714826.
Endogenous purine derivative of xanthine.
Synthesis impurity
5-Nitroimidazole derivative; genotoxic.
A third-generation ALK inhibitor.
Calpain I/II inhibitor.
Synthetis peptide, melanocortin analog; MCR ago...
HDAC inhibitor.
Synthetic catechol; ER agonist, microtubule pol...
Zinc chelator
Alkaloid found in black and long peppers; TRPV1...
Fluoroquinolone, S-(-) isomer of ofloxacin; top...
AMPA positive allosteric modulator, D2, 5-HT2A,...
T-type Ca2+ and voltage-gated Na+ channel block...
Coumarin; VKORC1 inhibitor.
Xanthine oxidase inhibitor.
pan-Raf inhibitor.
Dibenzofuran produced by lichens.
Folic acid derivative
Renin inhibitor.
EGFR and PDGFR inhibitor