F133
Norfluoxetine hydrochloride
≥97%, solid
别名:
(±)-γ-(4-Trifluoromethylphenoxy)benzenepropanamine hydrochloride
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关于此项目
经验公式（希尔记法）:
C16H16F3NO · HCl
化学文摘社编号:
分子量:
331.76
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
产品名称
Norfluoxetine hydrochloride, ≥97%, solid
InChI key
GMTWWEPBGGXBTO-UHFFFAOYSA-N
SMILES string
Cl[H].NCCC(Oc1ccc(cc1)C(F)(F)F)c2ccccc2
InChI
1S/C16H16F3NO.ClH/c17-16(18,19)13-6-8-14(9-7-13)21-15(10-11-20)12-4-2-1-3-5-12;/h1-9,15H,10-11,20H2;1H
assay
≥97%
form
solid
color
yellow
solubility
H2O: >4 mg/mL
DMSO: >5 mg/mL
Quality Level
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Application
Norfluoxetine hydrochloride has been used to examine if psychoactive pharmaceuticals in drinking water at environmental concentrations could induce neuronal gene expression. It has also been used to examine whether at environmental concentrations it can alter in vitro expression of autism spectrum disorders (ASD)-associated synaptic proteins in human neurons.
Biochem/physiol Actions
Fluoxetine metabolite; more potent inhibitor of serotonin uptake than fluoxetine with a half-life in vivo of 5-7 days.
Norfluoxetine is an active metabolite of fluoxetine. It disturbs the production of estrogen in a co-culture model of the feto-placental unit.
Disclaimer
Hygroscopic, photosensitive
Legal Information
Sold under license from Eli Lilly and Company.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Antônio Felipe Felicioni Oliveira et al.
Journal of pharmaceutical and biomedical analysis, 73, 53-58 (2012-05-05)
A two-phase liquid phase microextraction using a hollow fiber combined with injection port derivatization and gas chromatographic analysis was developed for extracting and detecting fluoxetine (FLU) and norfluoxetine (NOR) in human plasma. Simultaneous extraction in a multiple tube shaker was
Shaojun Shi et al.
Clinical therapeutics, 32(11), 1977-1986 (2010-11-26)
The proprietary formulation of fluoxetine hydrochloride is an antidepressant of the selective serotonin reuptake inhibitor class. Pharmacokinetic studies investigating the bioequivalence of generic and branded formulations are needed to market generic fluoxetine in China. The aim of this study was
Lushan Yu et al.
Journal of chromatography. A, 1236, 97-104 (2012-03-23)
In this study, we developed an LC-MS/MS method based on an isotope discrimination mass spectroscopy solution (IDMSS) technology to simultaneously quantify enantiomers of fluoxetine (FLX) and norfluoxetine (NFLX) in a CYP2C9 incubation mixture. S-FLX and S-NFLX were labeled to form
Jun Zuo et al.
Antimicrobial agents and chemotherapy, 56(9), 4838-4844 (2012-07-04)
No antiviral drugs currently exist for the treatment of enterovirus infections, which are often severe and potentially life threatening. Molecular screening of small molecule libraries identified fluoxetine, a selective serotonin reuptake inhibitor, as a potent inhibitor of coxsackievirus replication. Fluoxetine
D T Wong et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 8(4), 337-344 (1993-06-01)
Like fluoxetine, the N-demethylated metabolite norfluoxetine exists in R- and S-enantiomeric forms. S-Norfluoxetine inhibited serotonin (5-HT) uptake and [3H]paroxetine binding to 5-HT uptake sites with a pKi of 7.86 and 8.88 or 14 and 1.3 nM, respectively, whereas R-norfluoxetine was
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