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.
น้ำหนักโมเลกุล
352.5000 g/mol
LogP
3.70
TPSA
55.60 Ų
Lipinski RO5
ผ่าน
กลไกการออกฤทธิ์
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 …
โครงสร้าง 2 มิติ
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
พันธะที่หมุนได้
7
อะตอมหนัก
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.
คำถามที่พบบ่อย
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.
ข้อจำกัดความรับผิดชอบทางการแพทย์
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.
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