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norfluoxetine

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    8
    TargetMol | Inhibitors_Agonists
  • Isotope Products
    3
    TargetMol | Isotope_Products
norfluoxetine hydrochloride
Norfluoxetine HCl
T2102957226-68-3
Norfluoxetine Hydrochloride (Norfluoxetine HCl) is an active metabolite of fluoxetine. Fluoxetine is an antidepressant drug.
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TargetMol | Inhibitor Sale
Norfluoxetine
T8842583891-03-6
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10-14 weeks
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(S)-Norfluoxetine
T201552126924-38-7
(S)-Norfluoxetine, the S enantiomer of Norfluoxetine, functions as a selective serotonin reuptake inhibitor. It enhances allopregnanolone levels and reduces aggression in socially isolated mice.
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10-14 weeks
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(R)-Norfluoxetine
T204202130194-43-3
(R)-Norfluoxetine is the (R)-enantiomer of Norfluoxetine. It functions as a potent serotonin reuptake inhibitor, with a Ki value of 13 nM. This compound is utilized in the research of depression.
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10-14 weeks
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Norfluoxetine-d5 HCl
T713021185132-92-6
Norfluoxetine-d5 is intended for use as an internal standard for the quantification of norfluoxetine by GC- or LC-MS. Norfluoxetine is an active metabolite of the antidepressant fluoxetine. It is formed from fluoxetine by the cytochrome P450 (CYP) isoforms CYP2C9, CYP2C19, and CYP3A. Norfluoxetine inhibits serotonin (5-HT) uptake in rat brain synaptosomal membrane preparations (Ki = 44.7 nM) and isolated human platelets (IC50 = ~15 nM). It has been found in the tissues of fish exposed to wastewater effluent.
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35 days
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Norfluoxetine-d5 Hydrochloride
TMID-02171188265-34-0
Norfluoxetine-d5 Hydrochloride is a deuterated compound of Norfluoxetine Hydrochloride. Norfluoxetine Hydrochloride has a CAS number of 57226-68-3. Norfluoxetine hydrochloride is an active metabolite of fluoxetine. Fluoxetine is an antidepressant drug.
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35 days
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Seproxetine HCl
Seproxetine hydrochloride, (S)-Norfluoxetine hydrochloride, (S)-Desmethylfluoxetine Hydrochloride
T26184127685-30-7
Seproxetine HCl, a more active enantiomer of N-desmethyl metabolite fluoxetine, works by selectively inhibiting the serotonin uptake carrier.
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Pentoxifylline-d6
T713001185879-03-1
Pentoxifylline-d6 is intended for use as an internal standard for the quantification of pentoxifylline by GC- or LC-MS. Pentoxifylline is a hemorrheologic agent. It increases the deformability of washed isolated human erythrocytes when used at a concentration of 100 µM. Pentoxifylline (1, 2, and 3 mM) inhibits ADP-induced platelet aggregation in isolated human whole blood. It inhibits thrombus formation induced by ADP in a hamster cheek pouch model when administered at doses of 5, 10, and 20 mg kg. Formulations containing pentoxifylline have been used in the treatment of intermittent claudication.
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6-8 weeks
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