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Flumazenil - >99% (HPLC), high purity , CAS No.78755-81-4, Allosteric modulator of GABA A receptor α1 subunit;Allosteric modulator of GABA A receptor α2 subunit;Allosteric modulator of GABA A receptor α3 subunit;Allosteric modulator of GABA A receptor α4 subunit;Allosteric modulator of GABA A receptor α5 subunit;

  • Moligand™
  • ≥99%(HPLC)
Item Number
F124794
Grouped product items
SKUSizeAvailabilityPrice Qty
F124794-25mg
25mg
In stock
$53.90
F124794-100mg
100mg
In stock
$177.90
F124794-500mg
500mg
In stock
$801.90

Benzodiazepine antagonist

Basic Description

Synonymsflumazenil|78755-81-4|Anexate|Flumazepil|Romazicon|Lanexat|Mazicon|Ro 15-1788|fumazenil|Flumazenilum|Flumazenilo|Flumazenilum [Latin]|Ethyl 8-fluoro-5-methyl-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-3-carboxylate|Flumazenilo [Spanish]|Ro-
Specifications & PurityMoligand™, ≥99%(HPLC)
Biochemical and Physiological MechanismsFlumazenil, an imidazobenzodiazepine derivative, antagonizes the actions of benzodiazepines on the central nervous system. Flumazenil competitively inhibits the activity at the benzodiazepine recognition site on the GABA/benzodiazepine receptor complex. F
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeALLOSTERIC MODULATOR
Mechanism of actionAllosteric modulator of GABA A receptor α1 subunit;Allosteric modulator of GABA A receptor α2 subunit;Allosteric modulator of GABA A receptor α3 subunit;Allosteric modulator of GABA A receptor α4 subunit;Allosteric modulator of GABA A receptor α5 subunit;
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Flumazenil is a competitive GABAA receptor antagonist, used in the treatment of benzodiazepine overdoses.
A benzodiazepine antagonist

Product Properties

ALogP1

Names and Identifiers

IUPAC Name ethyl 8-fluoro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate
INCHI 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,3,7H2,1-2H3
InChi Key OFBIFZUFASYYRE-UHFFFAOYSA-N
Canonical SMILES CCOC(=O)C1=C2CN(C(=O)C3=C(N2C=N1)C=CC(=C3)F)C
Isomeric SMILES CCOC(=O)C1=C2CN(C(=O)C3=C(N2C=N1)C=CC(=C3)F)C
WGK Germany 2
RTECS NI2922170
Alternate CAS 78755-81-4
PubChem CID 3373
NSC Number 759193
MeSH Entry Terms Anexate;Flumazenil;Flumazepil;Lanexat;Ro 15 1788;Ro 15-1788;Ro 151788;Romazicon
Molecular Weight 303.29

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

4 results found

Lot NumberCertificate TypeDateItem
F1617092Certificate of AnalysisFeb 21, 2024 F124794
F2202197Certificate of AnalysisMar 18, 2022 F124794
F2202206Certificate of AnalysisMar 18, 2022 F124794
F2202207Certificate of AnalysisMar 18, 2022 F124794

Chemical and Physical Properties

SolubilitySoluble in DMSO to 25mM
SensitivityHeat Sensitive
Refractive Index1.63
Boil Point(°C)527.98 °C at 760 mmHg
Melt Point(°C)200 °C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H302:Harmful if swallowed

H332:Harmful if inhaled

H312+H332:Harmful in contact with skin or if inhaled

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P270:Do not eat, drink or smoke when using this product.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P362+P364:Take off contaminated clothing and wash it before reuse.

P330:Rinse mouth.

P301+P317:IF SWALLOWED: Get medical help.

P317:Get emergency medical help.

WGK Germany 2
RTECS NI2922170
Merck Index 4135

Related Documents

References

1. Huang Q, Liu R, Zhang P, He X, McKernan R, Gan T, Bennett DW, Cook JM.  (1998)  Predictive models for GABAA/benzodiazepine receptor subtypes: studies of quantitative structure-activity relationships for imidazobenzodiazepines at five recombinant GABAA/benzodiazepine receptor subtypes [alphaxbeta3gamma2 (x = 1-3, 5, and 6)] via comparative molecular field analysis..  J Med Chem,  41  (21): (4130-42).  [PMID:9767648]
2. Amato RJ et al..  (2010)  Effects of positive and negative modulators of the ?-aminobutyric acid A receptor complex on responding under a differential-reinforcement-of-low-rate schedule of reinforcement in rats..  Behav Pharmacol,      [PMID:20838210]
3. Amato RJ et al..  (2011)  Effects of pregnanolone and flunitrazepam on the retention of response sequences in rats..  Pharmacol Biochem Behav,  99  (3): (391-8).  [PMID:21640749]
4. Jin Z et al..  (2011)  Insulin reduces neuronal excitability by turning on GABA(A) channels that generate tonic current..  PLoS One,  (e16188).  [PMID:21264261]

Solution Calculators