您好,欢迎来到试剂仪器网! [登录] [免费注册]
试剂仪器网
位置:首页 > 产品库 > EMD 66684
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
EMD 66684
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。
EMD 66684图片
CAS NO:1216884-39-7
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
EMD 66684 是 II 型血管紧张素 (AT1) 受体的拮抗剂。EMD 66684 对 AT1 亚型Ang II受体具有强亲和力,IC50为 0.7 nM。EMD 66684 也是一种抗缺血的细胞保护剂。
生物活性

EMD 66684 is an antagonist ofAngiotensin II Type 1(AT1) receptor. EMD 66684 shows potent binding affinities for theAT1subtypeAng II receptorwith anIC50value of 0.7 nM. EMD 66684 also serves as an antiischemic cytoprotectant[1]-[5].

IC50& Target

Angiotensin II Type 1

0.7 nM (IC50)

体外研究
(In Vitro)

Ang II is known to activate at least two receptor subtypes, namely, AT1 and AT2 receptors[1].
EMD 66684 (0.1 μM) decreases Ang II (0.1 mM)-induced in basal and NS-induced NPY overflow, attenuates the NS-induced stimulation of both NE and NPY release[1].
EMD 66684 (0.01 nM-1 μM; 0, 30, 60 min) exhibits a time-dependent inhibition against Ang II in DMR (dynamic mass redistribution) responses, with IC50s of 181.97 nM (0 min), 0.22 nM (30 min), 0.17 nM (60 min), respectively[2].
EMD 66684 exhibits binding affinities for the AT1 subtype Ang II receptor with an IC50value of 0.7 nM in rat adrenal cortical membranes, and inhibits Ang II-Induced contraction in rabbit aortic rings with an IC50value of 0.2 nM[3].

Cell Viability Assay[1]

Cell Line:Hep G2 cells (liver hepatocellular carcinoma cell line)
Concentration:1 nM
Incubation Time:1 hour
Result:Completely blocked the Ang II responses Ang II-induced response.
体内研究
(In Vivo)

EMD 66684 (0.1, 0.3, 1 mg/kg; i.v.; once) results in a long lasting fall in blood pressure[3].
EMD 66684 (0.1 μM; 45 min) decreases the NS-induced overflow of NE and NPY from preparations from SHRs at 10-12 weeks old[4].

Animal Model:Conscious furosemide-treated SHR (Spontaneous Hypertension Rat)[3]
Dosage:0.1, 0.3, 1 mg/kg
Administration:Intravenous injection; once; as potassium salts to conscious furosemide-treated SHR
Result:Showed a long lasting fall in blood pressure, resulted mean arterial pressure (MAP) decreased in a dose-dependent manner.
分子量

547.05

Formula

C28H31ClN8O2

CAS 号

1216884-39-7

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.