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MRS2279
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
MRS2279图片
CAS NO:367909-40-8
包装:1mg

MRS2279 是一种选择性、高亲和力的P2Y1受体拮抗剂,Ki为 2.5 nM,IC50为 51.6 nM。MRS2279 竞争性抑制 ADP 促进的血小板聚集,并具有亲和性 (pKB=8.05)
生物活性

MRS2279 is a selective and high affinityP2Y1receptor antagonist, with aKiof 2.5 nM and anIC50of 51.6 nM. MRS2279 competitively inhibits ADP-promoted platelet aggregation with an apparent affnity (pKB=8.05)[1][2][3].

IC50& Target

P2Y1 Receptor

51.6 nM (IC50)

体外研究
(In Vitro)

MRS2279 antagonizes 2-MeSADP-stimulated inositol phosphate formation in turkey erythrocyte membranes with a pKbvalue of 7.75[2].
MRS2279 shows high affinity competitive antagonism to human P2Y1 receptor with a pKbvalue of 8.10 in 1321N1 human astrocytoma cells[2].
MRS2279 shows specific effect for the P2Y1 receptor, but shows no effect on activation of the human P2Y2, P2Y4, P2Y6, or P2Y11 receptors by their cognate agonists[2].
MRS2279 shows no ability to block the capacity of ADP to act through the Gi/adenylyl cyclase linked P2Y receptor of platelets to inhibit cyclic AMP accumulation[2].

体内研究
(In Vivo)

MRS2279 (2 μL, 1 nM; intracerebroventricular injection; 30 min prior to mechanical ventilation) reduces mouse brain injury induced by mechanical ventilation in high-pressure ventilation mice[3].

分子量

469.71

Formula

C13H18ClN5O8P2

CAS 号

367909-40-8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

 
 
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