Fentanyl Hydrochloride

CHEMBL1201159 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
372.9 g/mol
LogP
Phase
4

This medication is a salt form of fentanyl, a powerful opioid pain reliever used for severe or chronic pain that has not responded to other treatments. It works by binding to opioid receptors in the brain to block pain signals. Due to its high potency, it carries a significant risk of dependence and overdose.

分子量

372.9000 g/mol

TPSA

23.60 Ų

治疗领域

作用机制

Highly potent synthetic mu-opioid receptor agonist approximately 100 times more potent than morphine.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

机制

Highly potent synthetic mu-opioid receptor agonist approximately 100 times more potent than morphine.

二维结构

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SMILES

CCC(=O)N(c1ccccc1)C1CCN(CCc2ccccc2)CC1.Cl

InChI

InChI=1S/C22H28N2O.ClH/c1-2-22(25)24(20-11-7-4-8-12-20)21-14-17-23(18-15-21)16-13-19-9-5-3-6-10-19;/h3-12,21H,2,13-18H2,1H3;1H

Molecular Formula

C22H29ClN2O

HBD / HBA

1 / 2

可旋转键数

6

重原子数

26

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.

常见问题

This medication is a salt form of fentanyl, a powerful opioid pain reliever used for severe or chronic pain that has not responded to other treatments. It works by binding to opioid receptors in the brain to block pain signals. Due to its high potency, it carries a significant risk of dependence and overdose.

Highly potent synthetic mu-opioid receptor agonist approximately 100 times more potent than morphine.

Yes, Fentanyl 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). CHEMBL1201159. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 83932. Chemical information database.

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

医疗免责声明

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.