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Results for "

fluvoxamine

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    6
    TargetMol | Inhibitors_Agonists
  • Isotope Products
    2
    TargetMol | Isotope_Products
Fluvoxamine
T1077L54739-18-3
Fluvoxamine (DU-23000) is an antidepressant that functions as a selective serotonin reuptake inhibitor.
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7-10 days
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Fluvoxamine maleate
MK-264, DU-23000 (maleate)
T107761718-82-9
Fluvoxamine maleate (DU-23000 (maleate)) is a selective serotonin reuptake inhibitor that is used in the treatment of depression and a variety of anxiety disorders.
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Fluvoxamine acid
T6857984692-89-7
Fluvoxamine acid is a medication which functions as a selective serotonin reuptake inhibitor (SSRI) and σ1 receptor agonist. Fluvoxamine is used primarily for the treatment of obsessive-compulsive disorder (OCD), and is also used to treat major depressive disorder (MDD), and anxiety disorders such as panic disorder and post-traumatic stress disorder (PTSD).
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6-8 weeks
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Fluvoxamine-d4 maleate
TMID-0074
Fluvoxamine-d4 maleate is a deuterated compound of Fluvoxamine maleate. Fluvoxamine maleate has a CAS number of 61718-82-9. Fluvoxamine maleate is a selective serotonin reuptake inhibitor that is used in the treatment of depression and a variety of anxiety disorders.
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20 days
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Fluvoxamine-d3 Maleate
TMID-01861185245-56-0
Fluvoxamine-d3 Maleate is a deuterated compound of Fluvoxamine Maleate. Fluvoxamine Maleate has a CAS number of 61718-82-9. Fluvoxamine maleate is a selective serotonin reuptake inhibitor that is used in the treatment of depression and a variety of anxiety disorders.
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35 days
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Fluvoxketone
T6539061718-80-7
Fluvoxketone is trifluoromethyl-substituted aryl ketone compound useful as an intermediate in the synthesis of Fluvoxamine, which is a selective serotonin reuptake inhibitor. In the synthesis of Fluvoxamine, the ketone carbonyl of Fluvoxketone is elaborated to an oxime.In vitro,the inhibitory effect of fluvoxamine on actin polymerization was concentration dependent, and its IC50 was approximately 30 μM.In vivo,fluvoxamine treated EAE rats showed a decrease in IFN-γ serum levels and an increase in IL-4, pro- and anti-inflammatory cytokines respectively.
    7-10 days
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