Levomilnacipran Hydrochloride

CHEMBL2105732 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
282.8 g/mol
LogP
Phase
4

A hydrochloride salt form of levomilnacipran with the same therapeutic properties. An SNRI antidepressant with strong norepinephrine reuptake inhibition for major depressive disorder.

Masse moléculaire

282,8100 g/mol

TPSA

46,30 Ų

Aires thérapeutiques

Mécanisme d'action

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)

Mécanisme

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.

Structure 2D

SVG PNG

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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

Liaisons Rotatives

5

Atomes Lourds

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.

Foire aux questions

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 section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

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.

Avertissement médical

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.