Meperidine Hydrochloride

CHEMBL1701 Phase 4 Đã phê duyệt Small molecule

Half-Life

—

Bioavailability

—

Protein Binding

—

Molecular Weight

283.8 g/mol

LogP

—

Phase

4

A hydrochloride salt form of meperidine, a short-acting opioid pain reliever used for acute moderate-to-severe pain, typically in hospital settings for procedures or post-surgical pain management.

Khối lượng phân tử

283,7900 g/mol

TPSA

29,50 Å²

Lĩnh vực điều trị

Pancreatic Cancer Pain Management Non-Small Cell Lung Cancer Generalized Anxiety Disorder Stroke Obesity Breast Cancer Chronic Pain Hepatitis C

Cơ chế tác dụng

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)

Cơ chế

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 …

Cấu trúc 2D

SVG PNG

Cite this structure

Embed this structure

SMILES

CCOC(=O)C1(c2ccccc2)CCN(C)CC1.Cl

InChI

InChI=1S/C15H21NO2.ClH/c1-3-18-14(17)15(9-11-16(2)12-10-15)13-7-5-4-6-8-13;/h4-8H,3,9-12H2,1-2H3;1H

Molecular Formula

C15H22ClNO2

HBD / HBA

1 / 3

Liên kết có thể quay

4

Nguyên tử nặng

19

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.

Câu hỏi thường gặp

A hydrochloride salt form of meperidine, a short-acting opioid pain reliever used for acute moderate-to-severe pain, typically in hospital settings for procedures or post-surgical pain management.

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, Meperidine 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). CHEMBL1701. Open-access bioactivity database.
PubChem — National Center for Biotechnology Information (NCBI). CID 5750. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

PillFYI

Bạn đang tìm kiếm thông tin thân thiện với bệnh nhân?

Meperidine Hydrochloride trên PillFYI

Cấu trúc

Dữ liệu nhanh

Công thức: C15H22ClNO2
Tên đồng nghĩa: 2

Liên kết ngoài

Cite

BibTeX, APA, MLA, Chicago, IEEE, Harvard

Tuyên bố miễn trách y tế

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.