Levomilnacipran Hydrochloride
A hydrochloride salt form of levomilnacipran with the same therapeutic properties. An SNRI antidepressant with strong norepinephrine reuptake inhibition for major depressive disorder.
分子量
282.8100 g/mol
TPSA
46.30 Ų
治療領域
作用機序
Inhibits the reuptake of both serotonin and norepinephrine by blocking their respective presynaptic transporters. This dual mechanism enhances monoaminergic neurotransmission and produces antidepressant and analgesic effects.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits the reuptake of both serotonin and norepinephrine by blocking their respective presynaptic transporters. This dual mechanism enhances monoaminergic neurotransmission and produces antidepressant and analgesic effects.
2D構造
Cite this structure
Embed this structure
SMILES
CCN(CC)C(=O)[C@@]1(c2ccccc2)C[C@H]1CN.Cl
InChI
InChI=1S/C15H22N2O.ClH/c1-3-17(4-2)14(18)15(10-13(15)11-16)12-8-6-5-7-9-12;/h5-9,13H,3-4,10-11,16H2,1-2H3;1H/t13-,15+;/m0./s1
Molecular Formula
C15H23ClN2O
HBD / HBA
2 / 2
回転可能結合数
5
重原子数
19
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
よくある質問
A hydrochloride salt form of levomilnacipran with the same therapeutic properties. An SNRI antidepressant with strong norepinephrine reuptake inhibition for major depressive disorder.
Inhibits the reuptake of both serotonin and norepinephrine by blocking their respective presynaptic transporters. This dual mechanism enhances monoaminergic neurotransmission and produces antidepressant and analgesic effects.
Yes, Levomilnacipran Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2105732. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6917778. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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