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Fluvoxamine maleate

Fluvoxamine maleate

CAS: 61718-82-9

Molecular Formula: C19H25F3N2O6

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Fluvoxamine maleate - Names and Identifiers

Name Fluvoxamine maleate
Synonyms Fevarin
du23000
DU23000
Luvox CR
SME 3110
faverin50
UNII-5LGN83G74V
FLUVOXAMINE MALEATE
Fluvoxamine maleate
5-methoxy-4'-trifluoromethylvalerophenone(e)-o-2-aminoethyloximemonomaleate
1-pentanone,5-methoxy-1-(4-(trifluoromethyl)phenyl)-,o-(2-aminoethyl)oxime,(
5-Methoxy-4'-trifluoromethylvalerophenone (E)-O-2-aminoethyloxime monomaleate
(E)-5-methoxy-1-[4-(trifluoromethyl)phenyl]-O-(2-aminoethyl)oxime-1-pentanone
(E)-5-METHOXY-1-[4-(TRIFLUOROMETHYL)PHENYL]-1-PENTANONE-O-(2-AMINOETHYL)OXIME MALEATE
Fluvoxamine maleate,(E)-5-Methoxy-1-[4-(trifluoromethyl)phenyl]-1-pentanone-O-(2-aminoethyl)oxime maleate
CAS 61718-82-9
EINECS 612-212-6
InChI InChI=1/C15H21F3N2O2.C4H4O4/c1-21-10-3-2-4-14(20-22-11-9-19)12-5-7-13(8-6-12)15(16,17)18;5-3(6)1-2-4(7)8/h5-8H,2-4,9-11,19H2,1H3;1-2H,(H,5,6)(H,7,8)/b20-14+;2-1-
InChIKey LFMYNZPAVPMEGP-PIDGMYBPSA-N

Fluvoxamine maleate - Physico-chemical Properties

Molecular FormulaC19H25F3N2O6
Molar Mass434.41
Melting Point120-121.5 °C
Boling Point370.6 °C at 760 mmHg
Flash Point9℃
Solubility DMSO 87 mg/mL Water <1 mg/mL Ethanol 87 mg/mL
Appearancesolid
ColorWhite to Off-White
Merck14,4219
Storage Condition2-8°C
MDLMFCD00269809
UseA SR inhibitor which binds to the 5-HT transporter.
In vitro studyFluvoxamine increases the levels of [5-HT] in the prefrontal cortex and thalamus of rats and also increases the levels of [DA] in the striatum. Fluvoxamine maleate improves tactile allodynia through spinal 5-HT 2A/2C receptors, acting by acting on receptors or neurons of 5-HT.
In vivo studyFluvoxamine maleate also demonstrated antinociception in a dose-dependent manner in the paw stress test in non-ligated mice. Fluvoxamine maleate also induced an antinociceptive effect of the acute paw stress test, and this effect was antagonized by the 5-HT3 receptor antagonist granisetron. In the rat hippocampal medial prefrontal cortex (mPFC), Fluvoxamine(10 and 30 mg/kg, I. P.) enhanced hippocampal-mPFC pathway synaptic potency in a dose-dependent manner. In the hippocampal CA1 region of anesthetized rats, Fluvoxamine(10 and 30 mg/kg, I. P.) inhibited long-term potentiation (LTP). Fluvoxamine(30 mg/kg, I. P.) induced complete reversal of LTP for 5-HT(1A) receptor antagonist NAN-190(0.5 mg/kg, I. P.) but not 5-HT(4) the receptor antagonist GR113808(20 mg/rat, intraventricular injection) and 5-HT (7) receptor antagonist DR4004(10 mg/rat, intraventricular injection) were affected. Fluvoxamine maleate potentiates the response to norepinephrine in isolated rat vas deferens incubated in a Krebs-Henseleit solution. Fluvoxamine maleate and Fluoxetine hydrochloride inhibited the induction of contraction of isolated rat uterus preparations by potassium ions with IC50 of 3.99 μm and 18.2 μm, respectively.

Fluvoxamine maleate - Risk and Safety

Risk CodesR22 - Harmful if swallowed
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS36 - Wear suitable protective clothing.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S27 - Take off immediately all contaminated clothing.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
UN IDsUN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany3
RTECSSA9230000
HS Code29280000

Fluvoxamine maleate - Introduction

Fluvoxamine maleate is a selective serotonin reuptake inhibitor (SSRI).
Last Update:2022-10-16 17:27:11
Fluvoxamine maleate
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CAS: 61718-82-9
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CAS: 61718-82-9
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
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CAS: 61718-82-9
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View History
Fluvoxamine maleate
AP 10
SULFURIC ACID MONO(4-NITROPHENYL) ESTER POTASSIUM SALT
聚氧代乙烯(5)壬基苯基醚
2-[4-bromo-2-({[3-(4-morpholinyl)propyl]amino}methyl)phenoxy]-N-(2-methoxyphenyl)acetamide
(CHLOROMETHYL)DIMETHOXYMETHYLSILANE
L-Methionine p-nitroanilide
Cyclohexanone, 3-(phenylmethoxy)-2-[2-(phenylmethoxy)ethyl]-, trans-
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