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Fluoxetine hydrochloride

Catalog No. T0450L   CAS 56296-78-7
Synonyms: Fluoxetine HCl, LY-110140, Lilly110140

Fluoxetine hydrochloride (Lilly110140) is the first highly specific serotonin uptake inhibitor. It is used as an antidepressant and often has a more acceptable side-effects profile than traditional antidepressants.

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Fluoxetine hydrochloride Chemical Structure
Fluoxetine hydrochloride, CAS 56296-78-7
Pack Size Availability Price/USD Quantity
25 mg In stock $ 48.00
50 mg In stock $ 64.00
100 mg In stock $ 82.00
200 mg In stock $ 148.00
500 mg In stock $ 252.00
1 mL * 10 mM (in DMSO) In stock $ 63.00
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Purity: 99.66%
Purity: 99.66%
Purity: 99.6%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Fluoxetine hydrochloride (Lilly110140) is the first highly specific serotonin uptake inhibitor. It is used as an antidepressant and often has a more acceptable side-effects profile than traditional antidepressants.
In vitro When co-administered in adult male SD rats, fluoxetine and olanzapine induce a robust and sustained increase in extracellular dopamine levels, with concentrations surpassing baseline by 361% and 272%, respectively—significantly higher than when either drug is used alone. Additionally, fluoxetine reverses the prolonged latency of escape caused by unavoidable shocks in adult male SD rats.
In vivo Fluoxetine accelerates the maturation of immature neurons. It enhances the proliferation of new cells in the dentate gyrus of the adult rat hippocampus, strengthens neurodependent long-term potentiation in the hippocampal dentate gyrus, and increases the number of proliferating cells in the prefrontal cortex.
Synonyms Fluoxetine HCl, LY-110140, Lilly110140
Molecular Weight 345.787
Formula C17H19ClF3NO
CAS No. 56296-78-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: 3.5 mg/mL (10 mM)

DMSO: 34.6 mg/mL (100 mM)

TargetMolReferences and Literature

1. Malberg JE, et al. Neuropsychopharmacology, 2003, 28(9), 1562-1571. 2. Kodama M, et al. Biol Psychiatry, 2004, 56(8), 570-580. 3. Wang JW, et al. J Neurosci, 2008, 28(6), 1374-1384. 4. Bymaster FP, et al. Psychopharmacology (Berl), 2002, 160(4), 353-361. 5. Zhang W, et al. Neuropsychopharmacology, 2000, 23(3), 250-262. 6. Su WJ, et al. Antidiabetic drug glyburide modulates depressive-like behavior comorbid with insulin resistance. J Neuroinflammation. 2017 Oct 30;14(1):210. 7. Gao T T, Wang Y, Liu L, et al. LIMK1/2 in the mPFC plays a role in chronic stress-induced depressive-like effects in mice[J]. International Journal of Neuropsychopharmacology. 2020, 23(12): 821-836.

TargetMolCitations

1. Gao T T, Wang Y, Liu L, et al. LIMK1/2 in the mPFC plays a role in chronic stress-induced depressive-like effects in mice. International Journal of Neuropsychopharmacology. 2020, 23(12): 821-836. 2. Zeng J, Xie Z, Chen L, et al.Rosmarinic acid alleviate CORT-induced depressive-like behavior by promoting neurogenesis and regulating BDNF/TrkB/PI3K signaling axis.Biomedicine & Pharmacotherapy.2024, 170: 115994.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Approved Drug Library Anti-Cancer Drug Library Drug Repurposing Compound Library EMA Approved Drug Library Inhibitor Library GPCR Compound Library Anti-Neurodegenerative Disease Compound Library Anti-Cancer Compound Library Anti-Parkinson's Disease Compound Library NO PAINS Compound Library

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Keywords

Fluoxetine hydrochloride 56296-78-7 Autophagy GPCR/G Protein Neuroscience 5-HT Receptor Serotonin Transporter Fluoxetine HCl Fluoxetine SLC6A4 SERT inhibit Inhibitor LY 110140 5-HTT Fluoxetine Hydrochloride LY-110140 Lilly110140 LY110140 inhibitor

 

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