WARNING: This product is for research use only, not for human or veterinary use.
Hodoodo CAT#: H317890
CAS#: 56296-78-7 (HCl)
Description: Fluoxetine, also known by trade names Prozac and Sarafem among others, is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. It is used for the treatment of major depressive disorder, obsessive–compulsive disorder, bulimia nervosa, panic disorder, and premenstrual dysphoric disorder. It may decrease the risk of suicide in those over the age of 65. Fluoxetine has also been used to treat premature ejaculation. It is taken by mouth.
Hodoodo Cat#: H317890
Name: Fluoxetine HCl
CAS#: 56296-78-7 (HCl)
Chemical Formula: C17H19ClF3NO
Exact Mass: 0.00
Molecular Weight: 345.790
Elemental Analysis: C, 59.05; H, 5.54; Cl, 10.25; F, 16.48; N, 4.05; O, 4.63
Related CAS #: 54910-89-3 (free base) 56296-78-7 (HCl) 114414-02-7 (oxalate)
Synonym: Fluoxetine, Prozac, Sarafem, Fluoxetine, Animex-On, Fluoxetin, Pulvules, Eufor, Portal
IUPAC/Chemical Name: N-methyl-3-phenyl-3-(4-(trifluoromethyl)phenoxy)propan-1-amine hydrochloride
InChi Key: GIYXAJPCNFJEHY-UHFFFAOYSA-N
InChi Code: InChI=1S/C17H18F3NO.ClH/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20;/h2-10,16,21H,11-12H2,1H3;1H
SMILES Code: FC(C1=CC=C(OC(C2=CC=CC=C2)CCNC)C=C1)(F)F.[H]Cl
Appearance: Solid powder
Purity: >98% (or refer to the Certificate of Analysis)
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility: Soluble in DMSO, not in water
Shelf Life: >2 years if stored properly
Drug Formulation: This drug may be formulated in DMSO
Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code: 2922.39.4500
More Info:
Biological target: | Selective serotonin-reuptake inhibitor (SSRI) at the neuronal membrane |
In vitro activity: | Antidepressants have been demonstrated to induce activation of TRKB receptors in the brain. Moreover, fluoxetine, a widely used antidepressant, induces ocular dominance plasticity in the adult visual cortex through BDNF-TRKB signaling and reduces percentage of PNNs enwrapping PV+ interneurons in the amygdala and hippocampus, shifting PV+ interneurons toward an immature state and reopening brain plasticity. Therefore, it was questioned whether fluoxetine treatment might have an effect on TRKB:PTPσ interaction, which could potentially establish a link between antidepressant-induced pTRKB and PNNs. We cultured rat primary cortical neurons for 7 DIV and challenged them with two different doses of fluoxetine (0.1 and 1 μm) for 30 min. Fluoxetine dose-dependently reduced the interaction between TRKB and PTPσ in vitro as measured by ELISA (Fig. 3A). |
In vivo activity: | To validate the dysregulated protein synthesis and eventually the synaptic morphological changes, spine numbers were measured and analyzed with Golgi staining. Significantly reduced spines numbers (Fig.5l, m) were found in LPS-administrated mice as compared to fluoxetine-treated animals. Furthermore, serotonin receptor changes were investigated through which fluoxetine act as an antidepressant. Fluoxetine treatment significantly decreased LPS-mediated 5-hydroxytryptamine receptor (5HT-2A) and 5HT-2C expression in the mice hippocampus (Fig. a, g, and h). Besides, accumulating studies show dysregulated HDACs consequently lead to impaired acetylation and deacetylation in translational control, which could play a key role in the pathophysiological development of MDD. We then measured HDAC1, 2, and 3 expressions in the hippocampal tissues of the experimental animals. LPS administration significantly enhanced HDAC1 expression but not HDAC2 and HDAC3 expression, which could be substantially attenuated by fluoxetine (Fig.5a, i–k). |
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
DMF | 16.0 | 46.27 | |
DMSO | 38.7 | 111.89 | |
Ethanol | 40.8 | 117.85 | |
PBS (pH 7.2) | 0.2 | 0.58 | |
Water | 36.2 | 104.77 |
The following data is based on the product molecular weight 345.79 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 1.15 mL | 5.76 mL | 11.51 mL |
5 mM | 0.23 mL | 1.15 mL | 2.3 mL |
10 mM | 0.12 mL | 0.58 mL | 1.15 mL |
50 mM | 0.02 mL | 0.12 mL | 0.23 mL |
Formulation protocol: | 1. Lesnikova A, Casarotto PC, Fred SM, Voipio M, Winkel F, Steinzeig A, Antila H, Umemori J, Biojone C, Castrén E. Chondroitinase and Antidepressants Promote Plasticity by Releasing TRKB from Dephosphorylating Control of PTPσ in Parvalbumin Neurons. J Neurosci. 2021 Feb 3;41(5):972-980. doi: 10.1523/JNEUROSCI.2228-20.2020. Epub 2020 Dec 8. PMID: 33293360; PMCID: PMC7880295. 2. Li W, Ali T, Zheng C, Liu Z, He K, Shah FA, Ren Q, Rahman SU, Li N, Yu ZJ, Li S. Fluoxetine regulates eEF2 activity (phosphorylation) via HDAC1 inhibitory mechanism in an LPS-induced mouse model of depression. J Neuroinflammation. 2021 Feb 1;18(1):38. doi: 10.1186/s12974-021-02091-5. PMID: 33526073; PMCID: PMC7852137. |
In vitro protocol: | 1. Lesnikova A, Casarotto PC, Fred SM, Voipio M, Winkel F, Steinzeig A, Antila H, Umemori J, Biojone C, Castrén E. Chondroitinase and Antidepressants Promote Plasticity by Releasing TRKB from Dephosphorylating Control of PTPσ in Parvalbumin Neurons. J Neurosci. 2021 Feb 3;41(5):972-980. doi: 10.1523/JNEUROSCI.2228-20.2020. Epub 2020 Dec 8. PMID: 33293360; PMCID: PMC7880295. |
In vivo protocol: | 1. Li W, Ali T, Zheng C, Liu Z, He K, Shah FA, Ren Q, Rahman SU, Li N, Yu ZJ, Li S. Fluoxetine regulates eEF2 activity (phosphorylation) via HDAC1 inhibitory mechanism in an LPS-induced mouse model of depression. J Neuroinflammation. 2021 Feb 1;18(1):38. doi: 10.1186/s12974-021-02091-5. PMID: 33526073; PMCID: PMC7852137. |
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