1. Neuronal Signaling Protein Tyrosine Kinase/RTK PI3K/Akt/mTOR Membrane Transporter/Ion Channel
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  3. Levomilnacipran

Levomilnacipran  (Synonyms: (1S,2R)-Milnacipran; F2695)

Cat. No.: HY-14794A
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Levomilnacipran ((1S,2R)-Milnacipran) is the enantiomer of Milnacipran (HY-B0168) and a strong substrate of P-gp that can cross the blood-brain barrier. Levomilnacipran is a serotonin and norepinephrine reuptake inhibitor, with IC50 values of 10.5 nM and 19.0 nM, and Ki values of 92.2 nM and 1.2 nM for human norepinephrine transporter (NET) and serotonin transporter (SERT), respectively. Levomilnacipran has antidepressant and anxiolytic activities. Levomilnacipran hydrochloride can be used for the research of depression.

For research use only. We do not sell to patients.

Levomilnacipran Chemical Structure

Levomilnacipran Chemical Structure

CAS No. : 96847-54-0

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Description

Levomilnacipran ((1S,2R)-Milnacipran) is the enantiomer of Milnacipran (HY-B0168) and a strong substrate of P-gp that can cross the blood-brain barrier. Levomilnacipran is a serotonin and norepinephrine reuptake inhibitor, with IC50 values of 10.5 nM and 19.0 nM, and Ki values of 92.2 nM and 1.2 nM for human norepinephrine transporter (NET) and serotonin transporter (SERT), respectively. Levomilnacipran has antidepressant and anxiolytic activities. Levomilnacipran hydrochloride can be used for the research of depression[1][2][3][4].

In Vivo

Levomilnacipran (30 mg/kg; intraperitoneal injection; 10 days) exhibits antidepressant activity in LPS (HY-D1056)-induced depressed rat models[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Adult male Wistar rats aged 9 weeks old (200-220 g) treated LPS (HY-D1056)[3]
Dosage: 30 mg/kg
Administration: Intraperitoneal injection; 10 days
Result: Significantly ameliorated depression-like behaviors, including increasing sucrose preference in the SPT, reducing immobility time and increasing swimming time in the FST, and increasing the time spent in the central area in the OFT.
Improved neuronal synaptic deficits and morphological changes in the hippocampus, upregulated the expression of synaptic-related proteins PSD-95 and Syn, activated the BDNF/TrkB mediated PI3K/Akt/mTOR signaling pathway, and suppressed neuroinflammation by regulating the balance of pro- and anti-inflammatory cytokines in the hippocampus.
Clinical Trial
Molecular Weight

246.35

Formula

C15H22N2O

CAS No.
SMILES

O=C(N(CC)CC)[C@@]1([C@@H](C1)CN)C2=CC=CC=C2

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Room temperature in continental US; may vary elsewhere.

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Please store the product under the recommended conditions in the Certificate of Analysis.

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