| 货号:14050-1 mg | 规格:1 mg | 目录价:¥281 |
| 货号:14050-10 mg | 规格:10 mg | 目录价:¥2037 |
| 货号:14050-5 mg | 规格:5 mg | 目录价:¥1152 |
| 货号:14050-50 mg | 规格:50 mg | 目录价:¥8777 |
产品详情
* 以下信息仅供参考,详情请以原厂网站为准
产品名称:
AH 6809
产品描述:
AH 6809 is an EP and DP receptor antagonist with nearly equal affinity for the cloned human EP1, EP2, EP3-III, and DP1 receptors.{8322} AH 6809 blocks the PGE2-induced accumulation of cAMP in COS cells transfected with the human EP2 receptor.{3391} It also blocks the accumulation of Ca2+ in Xenopus oocytes expressing the human EP1 receptor.{3176} In the human and guinea pig, the activity profile of AH 6809 is similar to that of SC-19220, but it is somewhat more potent.{3409} In the mouse, AH 6809 has the highest affinity for the EP2 receptor, but also acts as a weak ligand at the murine EP1 and DP1 receptors.{6640} In whole human platelets, AH 6809 is an effective antagonist of the antiaggregatory actions of PGD2, but not PGI2, with an EC50 of about 5 x 10−5 M.{3319}
保存温度:
-20
运输温度:
-20
预期分子量:
298.3
产品形式:
A crystalline solid
纯度:
≥97%
CAS号:
33458-93-4
分子式:
C17H14O5
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