SC-51322 化学特性,用途語,生産方法
用途
強力な EP1 プロスタノイド受容体アンタゴニストです(Ki = 13.8 nM)。in vivo において鎮痛
作用を示します。
用途
強力な EP1 プロスタノイド受容体アンタゴニストです(Ki = 13.8 nmol/l)。in vivo において鎮
痛作用を示します。
説明
The prostaglandin E
2 (PGE
2) receptor (EP
1) is involved in triggering PGE
2-
mediated pain as well as neuronal survival and growth. SC-
51322 is a selective EP
1 antagonist that inhibits PGE
2 signaling in a guinea pig ileum muscle strip assay with a pA
2 value of 8.1 and demonstrates analgesic activity in a mouse writhing assay with an ED
50 value of 0.9 mg/kg. It is pharmacologically similar to SC-
51089, but does not release hydrazine, a known carcinogen to rats, as does SC-
51089. SC-
51322 potentiates the vasorelaxation of human pulmonary vein induced by PGE
2 with an EC
50 value of 7.75 μM.
化学的特性
Off-White Solid
使用
A selective E-prostanoid receptor subtype 1 (EP1) receptor antagonist which shows antihypertensive effects.
SC-51322 上流と下流の製品情報
原材料
準備製品