您好,欢迎来到试剂信息网! [登录] [免费注册]
试剂信息网
位置:首页 > 产品库 > A-779(trifluoroacetate salt)
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:
 
A-779(trifluoroacetate salt)
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。
A-779(trifluoroacetate salt)图片
规格:98%
分子量:873
包装与价格:
包装价格(元)
1mg电议
5mg电议
10mg电议
25mg电议

产品介绍
A neuropeptide with diverse biological activities
货号:ajcx21572
CAS:N/A
分子式:C39H60N12O11.XCF3COOH
分子量:873
溶解度:DMF: 10 mg/ml,DMSO: 33 mg/ml,PBS (pH 7.2): 1 mg/ml
纯度:98%
存储:Store at -20°C
库存:现货

Background:

A-779 is a peptide antagonist of the Mas receptor, also known as the angiotensin (1-7) (Ang (1-7)) receptor (IC50= 0.3 nM in a radioligand binding assay).1It does not compete with angiotensin 1 (AT1) and AT2receptor agonists for binding in adrenocortical membranes when used at a concentration of 1 µM and exhibits an IC50value greater than 10 µM in adrenomedullary membranes.2In vitro, A-779 inhibits Ang (1-7)-induced release of arachidonic acid from CHO cells transfected with Mas.1A-779 (0.01 mg/kg) prevents the antidiuretic effects of Ang (1-7) in water-loaded rats. It also inhibits the Ang (1-7)-induced decrease in mean arterial pressure (MAP) when administered by microinjection into the nucleus of the solitary tract with no effect on basal MAP. A-779 increases urine flow rate and sodium excretion in male, but not female, rats when AT1and AT2receptors are blocked by the selective antagonists losartan and PD 123319 , respectively.3


1.Santos, R.A., Simoes e Silva, A.C., Maric, C., et al.Angiotensin-(1-7) is an endogenous ligand for the G protein-coupled receptor MasProc. Natl. Acad. Sci. U.S.A.100(14)8258-8263(2003) 2.Santos, R.A., Campagnole-Santos, M.J., Baracho, N.C., et al.Characterization of a new angiotensin antagonist selective for angiotensin-(1-7): Evidence that the actions of angiotensin-(1-7) are mediated by specific angiotensin receptorsBrain Res. Bull.35(4)293-298(1994) 3.Mansoori, A.O., S., and Nematbakhsh, M.Role of Mas receptor antagonist (A779) on pressure diuresis and natriuresis and renal blood flow in the absence of angiotensin II receptors type 1 and 2 in female and male ratsJ. Physiol. Pharmacol.65(5)633-639(2014)