Zuranolone
Zuranolone is a neuroactive steroid and positive allosteric modulator of GABA-A receptors that binds to synaptic and extrasynaptic GABA-A receptor complexes, enhancing chloride ion conductance and overall inhibitory neurotransmission to reduce neuronal hyperexcitability associated with mood disorders. It is approved as a two-week oral treatment course for major depressive disorder and postpartum depression, offering rapid onset of antidepressant effects. Unlike SSRIs, it targets GABAergic rather than monoaminergic pathways, potentially addressing neurobiological underpinnings of depression related to GABA deficiency.
分子量
409.6000 g/mol
LogP
4.50
TPSA
78.90 Ų
リピンスキーの五則
適合
治療領域
Pharmacokinetics (PK)
Pharmacodynamics (PD)
2D構造
Cite this structure
Embed this structure
SMILES
C[C@@]1(O)CC[C@H]2[C@H](CC[C@@H]3[C@@H]2CC[C@]2(C)[C@@H](C(=O)Cn4cc(C#N)cn4)CC[C@@H]32)C1
InChI
InChI=1S/C25H35N3O2/c1-24(30)9-7-18-17(11-24)3-4-20-19(18)8-10-25(2)21(20)5-6-22(25)23(29)15-28-14-16(12-26)13-27-28/h13-14,17-22,30H,3-11,15H2,1-2H3/t17-,18+,19-,20-,21+,22-,24-,25+/m1/s1
Molecular Formula
C25H35N3O2
HBD / HBA
1 / 4
回転可能結合数
3
重原子数
30
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
Zuranolone is a neuroactive steroid and positive allosteric modulator of GABA-A receptors that binds to synaptic and extrasynaptic GABA-A receptor complexes, enhancing chloride ion conductance and overall inhibitory neurotransmission to reduce neuronal hyperexcitability associated with mood disorders. It is approved as a two-week oral treatment course for major depressive disorder and postpartum depression, offering rapid onset of antidepressant effects. Unlike SSRIs, it targets GABAergic rather than monoaminergic pathways, potentially addressing neurobiological underpinnings of depression related to GABA deficiency.
Yes, Zuranolone 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). CHEMBL4105630. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 86294073. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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