双氯芬酸依波拉明

双氯芬酸依波拉明（CAS 119623-66-4）的公开数据库记录，列此仅供独立核对。

危险化学品分类与危害说明

这个物质在各数据库里的编号

数据库记载的用途

• For the acute and chronic treatment of signs and symptoms of osteoarthritis and rheumatoid arthritis.
• Breast Feeding; Lactation; Milk, Human; Analgesic Agents; Anti-inflammatory Agents, Nonsteroidal
• Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.
• Anti-Inflammatory Agents, Non-Steroidal [CS]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]; Cyclooxygenase Inhibitors [MoA]
• Hepatic. Route of Elimination: Diclofenac is eliminated through metabolism and subsequent urinary and biliary excretion of the glucuronide and the sulfate conjugates of the metabolites. Little or no free unchanged diclofenac is excreted in the urine. Approximately 65% of the dose is excreted in the urine and approximately 35% in the bile as conjugates of unchanged diclofenac plus metabolites. Half Life: 2 hours

它在各数据库里的别名

diclofenac epolamine; 119623-66-4; Flector; DHEP; DIEP; Diclofenac hydroxyethylpyrrolidine; Diclofenac-epolamine; Diclofenac epolaminum; X5F8EKL9ZG; LICART; Diclofenac-N-(2-hydroxyethyl) pyrrolidine; DTXSID80152531; Diclofenac 1-(2-hydroxyethyl)pyrrolidinium salt; N-(2-Hydroxyethyl)pyrrolidinium (2-((2,6-dichlorophenyl)amino)phenyl)acetate; CHEBI:48296; RefChem:57630

计算机算出的分子描述符

数据库摘要

Diclofenac epolamine · CAS 119623-66-4 · C20H24Cl2N2O3. UNII X5F8EKL9ZG.

数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。