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Fluoxetine Hydrochloride

Fluoxetine Hydrochloride

Product ID F4780
Cas No. 56296-78-7
Purity ≥98%
Product Unit SizeCostQuantityStock
1 g $96.00 In stock
5 g $382.10 In stock
Bulk Quote

Quicklinks

  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Custom Order

Description

Fluoxetine is an SSRI most often used to treat mood or psychiatric disorders such as depression, obsessive compulsive disorder, bulimia nervosa, panic disorder, and PTSD. Fluoxetine inhibits 5-HT reuptake acting as an antagonist at 5-HT transporters (SERTs) as well as at 5-HT receptors and σ1 receptors. Likely related to its antidepressant activities, fluoxetine can prevent cue- and stress-induced reinstatement in animal models of substance abuse. In a clinical setting, fluoxetine increased abstinence rates in former female heroin-dependent subjects when combined with naltrexone compared to naltrexone alone. Additionally, this compound exhibits antiviral activity, demonstrated by its ability to reduce synthesis of coxsackievirus RNA and protein. Fluoxetine also acts as a functional inhibitor of acid sphingomyelinase (FIASMA).

pH value: 5-7 (5% aqueous solution)

Product Info

Cas No.

56296-78-7

Purity

≥98%

Formula

C17H18F3NO • HCl

Formula Wt.

345.79

Chemical Name

N-Methyl-γ-[4-(trifluoromethyl)phenoxy]benzene- propanamine hydrochloride

IUPAC Name

N-methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-amine; hydrochloride

Synonym

Adofen, Fluoxeren, Lovan, Prozac, Sarafem

Melting Point

158.4-158.9°C

Solubility

Soluble in methanol, ethanol, acetone, acetonitrile and chloroform. Water to 10 mM, DMSO to 100 mM. DMF to 16 mg/mL.Ethanol to 69mg/mL

Appearance

White Crystal Powder

Shipping and Storage

Store Temp

Ambient

Ship Temp

Ambient

Downloads

MSDS

F4780 MSDS PDF

Info Sheet

F4780 Info Sheet PDF

References

Zuo J, Quinn KK, Kye S, et al. Fluoxetine is a potent inhibitor of coxsackievirus replication. Antimicrob Agents Chemother. 2012 Sep;56(9):4838-44. PMID: 22751539.

Apparsundaram S, Stockdale DJ, Henningsen RA, et al. Antidepressants targeting the serotonin reuptake transporter act via a competitive mechanism. J Pharmacol Exp Ther. 2008 Dec;327(3):982-90. PMID: 18801947.

Krupitsky EM, Zvartau EE, Masalov DV, et al. Naltrexone with or without fluoxetine for preventing relapse to heroin addiction in St. Petersburg, Russia. J Subst Abuse Treat. 2006 Dec;31(4):319-28. PMID: 17084785.

Pälvimäki EP, Roth BL, Majasuo H, et al. Interactions of selective serotonin reuptake inhibitors with the serotonin 5-HT2c receptor. Psychopharmacology (Berl). 1996 Aug;126(3):234-40. PMID: 8876023.

Narita N, Hashimoto K, Tomitaka S, et al. Interactions of selective serotonin reuptake inhibitors with subtypes of sigma receptors in rat brain. Eur J Pharmacol. 1996 Jun 20;307(1):117-9. PMID: 8831113.

Opal MD, Klenotich SC, Morais M, et al. Serotonin 2C receptor antagonists induce fast-onset antidepressant effects. Mol Psychiatry. 2014 Oct;19(10):1106-1114. PMID: 24166413.

Nagano M, Liu M, Inagaki H, et al. Early intervention with fluoxetine reverses abnormalities in the serotonergic system and behavior of rats exposed prenatally to dexamethasone. Neuropharmacology. 2012 Aug;63(2):292-300. PMID: 22710353.

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