2614W94

Modify Date: 2024-01-14 17:10:22

2614W94 Structure
2614W94 structure
Common Name 2614W94
CAS Number 205187-35-5 Molecular Weight 344.306
Density 1.5±0.1 g/cm3 Boiling Point 440.8±45.0 °C at 760 mmHg
Molecular Formula C15H11F3O4S Melting Point N/A
MSDS N/A Flash Point 220.4±28.7 °C

 Use of 2614W94


2614W94 is a selective, reversible inhibitor of monoamine oxidase-A with a competitive mechanism of inhibition and IC50 of 5 nM and Ki of 1.6 nM with serotonin as substrate.

 Names

Name 2614W94
Synonym More Synonyms

 2614W94 Biological Activity

Description 2614W94 is a selective, reversible inhibitor of monoamine oxidase-A with a competitive mechanism of inhibition and IC50 of 5 nM and Ki of 1.6 nM with serotonin as substrate.
Related Catalog
Target

IC50: 5 nM (Monoamine Oxidase)[1] Ki: 1.6 nM (Monoamine Oxidase)[1]

In Vitro 2614W94 shows potent inhibitory activity against MAO-A, but shows no inhibition of MAO-B at 30 nM[1].
In Vivo 2614W94 (5 mg/kg, p.o.) produces selective inhibition of MAO-A in brains and livers of rats. 2614W94 (5 mg/kg, p.o.) also causes an elevation of neurotransmitter amines in brain, inparticular serotonin and norepinephrine, with a concomitant decrease in their oxidized metabolites. 2614W94 (0.5, 1, 2 mg/kg, p.o.) potentiates 5-hydroxytryptophan-induced head twitches in rats in a dose-dependent manner, with an extrapolated ED50 of 1.1 mg/kg[1].
Kinase Assay MAO-A and -B forms are assayed. Rat brain mito-chondrial extract is pre-incubated with the inhibitor for 15 min at 37°C in 50 mM potassium phosphate buffer (pH 7.4). Substrates [3H]serotonin (0.2 mM, 5 Ci/mol) and [14C]β-phene-thylamine (10 µM, 3 Ci/mol) are then added, and incubation at 37°C is continued for 20 min. Blank assays contain 2 mM pargyline to inhibit all MAO activity. The reaction is terminated with 0.2 mL of 2 N HCl, and products are extracted with 6 mL of ethyl acetate/toluene (1:1). A 4 mL aliquot of the organic layer is countedin 10 mL of Ecolite in a scintillation spectrometer programmed for double-label counting. Assays are performed in triplicate unless otherwise indicated. At the above concentrations, serotonin is a selective substrate for MAO-A, and β-phenethylamine is aselective substrate for MAO-B.
Animal Admin Rats: Nonfasted Sprague-Dawley male rats (250-350 g) are dosed by gavage with 0.5% methyl cellulose or with 2614W94 or other compounds suspended in the methyl cellulose vehicle. For all groups, n = 3 unless otherwise specified. For oral administration, dosing volume is 10 mL/kg of body weight. For intravenous dosing, the vehicle is a mixture of PEG 400 (polyethylene glycol; molecular weight, 400), ethanol, and physiologic saline in a volume ratio of 1.5/1.5/1.0, respectively, and the dosing volume is 1 mL/kg. After dosing, rats are returned to their cages and allowed free access to water. Any animals kept overnight are also given food. Death is by CO2 asphyxiation, after which brains and livers are promptly removed, frozen on dry ice, and stored at -70°C.
References

[1]. Helen L. White, et al. Biochemical and Pharmacologic Properties of 2614W94, a Reversible, Competitive Inhibitor of MonoamineOxidase-A. DRUG DEVELOPMENT RESEARCH 45:1-9 (1998).

 Chemical & Physical Properties

Density 1.5±0.1 g/cm3
Boiling Point 440.8±45.0 °C at 760 mmHg
Molecular Formula C15H11F3O4S
Molecular Weight 344.306
Flash Point 220.4±28.7 °C
Exact Mass 344.033020
LogP 3.33
Vapour Pressure 0.0±1.0 mmHg at 25°C
Index of Refraction 1.553
Storage condition 2-8℃

 Synonyms

Phenoxathiin, 3-(2,2,2-trifluoro-1-methylethoxy)-, 10,10-dioxide
3-[(1,1,1-Trifluoro-2-propanyl)oxy]phenoxathiine 10,10-dioxide
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