Befloxatone
- Product Name
- Befloxatone
- CAS No.
- 134564-82-2
- Chemical Name
- Befloxatone
- Synonyms
- 503;MD-370;MD370503;MD-370503;MD 370503;Befloxatone;(R)-5-(methoxymethyl)-3-(4-((R)-4,4,4-trifluoro-3-hydroxybutoxy)phenyl)oxazolidin-2-one;2-Oxazolidinone, 5-(methoxymethyl)-3-[4-[(3R)-4,4,4-trifluoro-3-hydroxybutoxy]phenyl]-, (5R)-
- CBNumber
- CB2874979
- Molecular Formula
- C15H18F3NO5
- Formula Weight
- 349.3
- MOL File
- 134564-82-2.mol
Befloxatone Property
- Melting point:
- 101°
- alpha
- D20 -11.5° (c = 1 in methylene chloride)
- Boiling point:
- 447.3±45.0 °C(Predicted)
- Density
- 1.326±0.06 g/cm3(Predicted)
- pka
- 12.13±0.20(Predicted)
N-Bromosuccinimide Price
- Product number
- API0010777
- Product name
- BEFLOXATONE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $501.2
- Updated
- 2021/12/16
Befloxatone Chemical Properties,Usage,Production
Uses
Befloxatone is a selective and reversible inhibitor of monoamine oxidase A. A third line agent for the treatment of resistant depression.
in vivo
Befloxatone (0.75 mg/kg; i.p.; single dose) increases tissue levels of monoamines and decreases levels of their deaminating metabolites in rats[1].
Befloxatone (1 mg/kg; i.p.; single dose) induces elevated levels of dopamine and corticonorepinephrine in the extracellular striatum of rats, but not elevates levels of corticoserotonin[1].
Befloxatone (0.03-0.3 mg/kg; p.o.; single dose) effectively inhibits the firing rate of serotonergic neurons and partially reduces the firing of norepinephric neurons, but had no effect on the firing of dopaminergic neurons in rats[1].
Befloxatone (1.5 mg/kg; p.o.; single dose) does not enhance the pressor effect of the central active dose of oral tyramine and has a broad safety profile in rats[1].
IC 50
MAO-A: 4 nM (IC50); MAO-B: 300 nM (IC50)
Befloxatone Preparation Products And Raw materials
Raw materials
Preparation Products
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