物质信息

ID:1412

名称和标识
IUPAC传统名
etoricoxib
IUPAC标准名
5-chloro-3-(4-methanesulfonylphenyl)-2-(6-methylpyridin-3-yl)pyridine
商标名
TauxibNucoxiaAlgixArcoxia
别名
etoricoxibMK-663Etoricoxib
数据登录号
PubChem SID
PubChem CID
化合物性质
暂无数据
点击上传数据
描述信息
Drug Groups
approved; investigational
Description
Etoricoxib is a new COX-2 selective inhibitor. Current therapeutic indications are: treatment of rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, chronic low back pain, acute pain and gout. Like any other COX-2 selective inhibitor, Etoricoxib selectively inhibits isoform 2 of cyclo-oxigenase enzyme (COX-2). This reduces the generation of prostaglandins (PGs) from arachidonic acid.
Indication
For the treatment of rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, chronic low back pain, acute pain and gout.
Pharmacology
Etoricoxib is a COX-2 selective inhibitor (approximately 106 times more selective for COX-2 inhibition over COX-1). Currently it is approved in more than 60 countries worldwide but not in the US, where the Food and Drug Administration (FDA) require additional safety and efficacy data for etoricoxib before it will issue approval.
Toxicity
This reduced activity is the cause of reduced gastrointestinal toxicity, as demonstrated in several large clinical trials performed with different COXIB (see below links on NEJM and The Lancet). Some clinical trials and meta-analysis showed that treatment with COXIB lead to increased incidence of cardiovascular adverse events compared to placebo
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic, primarily via CYP3A4.
Absorption
Bioavailability is 100% following oral administration.
Half Life
22 hours
Protein Binding
92%
External Links
分子图谱
暂无数据
点击上传数据
参考文献
暂无数据
点击上传数据