Anileridine
An opioid analgesic that binds to mu-opioid receptors in the brain and spinal cord to relieve moderate to severe pain. Like other opioids, it carries risks of respiratory depression, dependence, and tolerance.
分子量
352.5000 g/mol
LogP
3.70
TPSA
55.60 Ų
リピンスキーの五則
適合
作用機序
Binds to mu (μ), kappa (κ), and/or delta (δ) opioid receptors in the central and peripheral nervous system, mimicking endogenous endorphins. Activation of these G-protein-coupled receptors inhibits pain signal transmission and modulates the emotional response to pain.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Binds to mu (μ), kappa (κ), and/or delta (δ) opioid receptors in the central and peripheral nervous system, mimicking endogenous endorphins. Activation of these G-protein-coupled receptors inhibits pain signal transmission …
2D構造
Cite this structure
Embed this structure
SMILES
CCOC(=O)C1(c2ccccc2)CCN(CCc2ccc(N)cc2)CC1
InChI
InChI=1S/C22H28N2O2/c1-2-26-21(25)22(19-6-4-3-5-7-19)13-16-24(17-14-22)15-12-18-8-10-20(23)11-9-18/h3-11H,2,12-17,23H2,1H3
Molecular Formula
C22H28N2O2
HBD / HBA
1 / 4
回転可能結合数
7
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.
よくある質問
An opioid analgesic that binds to mu-opioid receptors in the brain and spinal cord to relieve moderate to severe pain. Like other opioids, it carries risks of respiratory depression, dependence, and tolerance.
Binds to mu (μ), kappa (κ), and/or delta (δ) opioid receptors in the central and peripheral nervous system, mimicking endogenous endorphins. Activation of these G-protein-coupled receptors inhibits pain signal transmission and modulates the emotional response to pain.
Yes, Anileridine 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). CHEMBL1201347. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 8944. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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