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氟比洛芬

产品号 447994 公司名称 Sigma Aldrich
CAS号 5104-49-4 公司网站 http://www.sigmaaldrich.com
分子式 C15H13FO2 电 话 1-800-521-8956
分子量 244.2609232 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 593

产品价格信息

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产品别名

标题
Flurbiprofen
IUPAC标准名
2-(3-fluoro-4-phenylphenyl)propanoic acid
IUPAC传统名
flurbiprofen
别名
L-790,330
(±)-2-Fluoro-α-methyl-4-biphenylacetic acid
(±)-2-氟-α-甲基-4-联苯基乙酸

产品登记号

MDL号 MFCD00079303
EC号 225-827-6
CAS号 5104-49-4

产品性质

线性分子式 C6H5C6H3(F)CH(CH3)CO2H
纯度 97%
熔点 110-112 °C(lit.)
GHS危险品标识 GHS06
GHS警示词 Danger
GHS危险声明 H301
欧盟危险性物质标志 有毒(Toxic) 有毒(Toxic) (T)
MSDS下载 下载链接
个人保护装置 Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS警示性声明 P301 + P310
RID/ADR UN 2811 6.1/PG 3
危险公开号 25
RTECS编号 DU8341000
安全公开号 36/37/39-45
联合国危险货物等级 6.1
联合国危险货物编号 2811
联合国危险货物包装类别(PG) 3
德国WGK号 3

产品详细信息

详细说明 (English)
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.
详细说明 (简体中文)
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.

参考文献