物质信息

ID:182315

名称和标识
IUPAC传统名
flurbiprofen
IUPAC标准名
2-(3-fluoro-4-phenylphenyl)propanoic acid
别名
Flurbiprofen氟比洛芬(±)-2-氟-α-甲基-4-联苯基乙酸L-790,330
数据登录号
CAS号
PubChem SID
化合物性质
药理学性质
相关基因信息
human ... ALB(213), APP(351), CYP1A2(1544), CYP2C9(1559)rat ... Ptgs1(24693)
安全信息
RID/ADR
UN 2811 6.1/PG 3
GHS警示词
Danger
联合国危险货物编号
2811
GHS危险声明
H301
安全公开号
36/37/39-45
德国WGK号
3
联合国危险货物包装类别(PG)
3
欧盟危险性物质标志
有毒 有毒 (T)
危险公开号
25
RTECS编号
DU8341000
联合国危险货物等级
6.1
GHS危险品标识
GHS06
急性毒性(口服,皮肤接触,吸入),类别1,2,3
个人保护装置
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS警示性声明
P301+P310
理化性质
熔点
110-112 °C(lit.)
描述信息
Application
Flurbiprofen is a nonsteroidal anti-inflammatory agent (NSAIA) with antipyretic, analgesic, and antifungal activity. Oral formulations of flurbiprofen may be used to treat rheumatoid arthritis, osteoarthritis and anklylosing spondylitis. Flurbiprofen is also used topically during ocular surgery to prevent or reduce intraoperative miosis. Flurbiprofen is structurally and pharmacologically related to ibuprofen. It is used to study the pathophysiological steps of NSAID enteropathy in the rat1 and the biotransformation of flurbiprofen by Cunninghamella species2.
Biochem/physiol Actions
Fluibiprofen is a cyclooxygenase (COX) inhibitor, which is an enzyme responsible for the conversion of arachidonic acid to prostaglandin G2 (PGG2) and PGG2 to prostaglandin H2 (PGH2) in the prostaglandin synthesis pathway. This decreases the prostaglandins which cause inflammation, pain, swelling and fever. Flurbiprofen inhibits the activity of both COX-1 and -2. The S enantiomer inhibits prostaglandin synthesis and has both anti-inflammatory and analgesic activity, while the R enantiomer does not inhibit prostaglandin synthesis and displays only analgesic activity.
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