Dantrolene

CHEMBL1201288 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
314.2 g/mol
LogP
1.7
Phase
4

A muscle relaxant that acts directly on skeletal muscle by inhibiting calcium release from the sarcoplasmic reticulum, used to treat malignant hyperthermia, neuroleptic malignant syndrome, and chronic spasticity. It is the only drug effective for the life-threatening muscle rigidity of malignant hyperthermia.

分子量

314.2500 g/mol

LogP

1.70

TPSA

121.00 Ų

リピンスキーの五則

適合

治療領域

作用機序

Reduces skeletal muscle tone and spasm through central or peripheral mechanisms, typically by modulating spinal reflexes, enhancing inhibitory neurotransmission, or blocking neuromuscular transmission.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Reduces skeletal muscle tone and spasm through central or peripheral mechanisms, typically by modulating spinal reflexes, enhancing inhibitory neurotransmission, or blocking neuromuscular transmission.

2D構造

SVG PNG

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SMILES

O=C1CN(/N=C/c2ccc(-c3ccc([N+](=O)[O-])cc3)o2)C(=O)N1

InChI

InChI=1S/C14H10N4O5/c19-13-8-17(14(20)16-13)15-7-11-5-6-12(23-11)9-1-3-10(4-2-9)18(21)22/h1-7H,8H2,(H,16,19,20)/b15-7+

Molecular Formula

C14H10N4O5

HBD / HBA

1 / 6

回転可能結合数

3

重原子数

23

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 muscle relaxant that acts directly on skeletal muscle by inhibiting calcium release from the sarcoplasmic reticulum, used to treat malignant hyperthermia, neuroleptic malignant syndrome, and chronic spasticity. It is the only drug effective for the life-threatening muscle rigidity of malignant hyperthermia.

Reduces skeletal muscle tone and spasm through central or peripheral mechanisms, typically by modulating spinal reflexes, enhancing inhibitory neurotransmission, or blocking neuromuscular transmission.

Yes, Dantrolene 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). CHEMBL1201288. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6914273. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

医学的免責事項

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.