Fluvoxamine maleate
CAS No. 61718-82-9
Fluvoxamine maleate ( Fevarin; Floxyfral; Luvox; MK-264; NSC 309469 )
Catalog No. M15334 CAS No. 61718-82-9
Fluvoxamine maleate is a selective serotonin (5-HT) reuptake inhibitor (SSRI).
Purity : >98%(HPLC)
Size | Price / USD | Stock | Quantity |
10MG | 42 | In Stock |
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25MG | 57 | In Stock |
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50MG | 69 | In Stock |
|
100MG | 105 | In Stock |
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200MG | 156 | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
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Biological Information
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Product NameFluvoxamine maleate
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NoteResearch use only, not for human use.
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Brief DescriptionFluvoxamine maleate is a selective serotonin (5-HT) reuptake inhibitor (SSRI).
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DescriptionFluvoxamine maleate is a selective serotonin (5-HT) reuptake inhibitor (SSRI).
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SynonymsFevarin; Floxyfral; Luvox; MK-264; NSC 309469
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PathwayEndocrinology/Hormones
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Target5-HT Receptor
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Recptor5-HT
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number61718-82-9
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Formula Weight434.41
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Molecular FormulaC19H25F3N2O6
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Purity>98%(HPLC)
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SolubilityEthanol: 87 mg/mL (200.27 mM); DMSO: 87 mg/mL (200.27 mM)
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SMILESCOCCCC/C(=N\OCCN)/C1=CC=C(C=C1)C(F)(F)F.C(=C\C(=O)O)\C(=O)O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Astragaloside
Astragaloside IV, an active component isolated from Astragalus membranaceus, suppresses the activation of ERK1/2 and JNK, and downregulates matrix metalloproteases (MMP)-2, (MMP)-9 in MDA-MB-231 breast cancer cells.
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SEP-363856 hydrochlo...
SEP-363856 hydrochloride is an agent of orally active and CNS active psychotropic with a unique, non-D2/5-HT2A mechanism of action, exerts its antipsychotic-like effects, has the potential to treatment of schizophrenia. SEP-856 (10μM) specifically inhibits α2A, α2B, D2, 5-HT1A, 5-HT1B, 5-HT1D, 5-HT2A, 5-HT2B, 5-HT2C and 5-HT7> 50% receptor.
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PRX-07034
PRX-07034 is a selective antagonist of 5-HT6 receptor. It has cognition and memory-enhancing properties and potently decreases food intake and body weight in rodents.?PRX-07034 is both a potent (Ki = 4-8 nM) and highly selective 5-HT(6) receptor antagonist (≥100-fold selectivity for the 5-HT(6) receptor compared to 68 other GPCRs, ion channels, and transporters, except D(3) (Ki = 71 nM) and 5-HT(1B) (Ki = 260 nM) receptors.