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 > Urocortin II(human)(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:
 
Urocortin II(human)(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。
Urocortin II(human)(trifluoroacetate salt)图片
CAS NO:398001-88-2
规格:98%
分子量:4450.2
包装与价格:
包装价格(元)
500ug电议
1mg电议

产品介绍
Urocortin II is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF , urocortin , urocortin III , frog sauvagine, and piscine urotensin I.
CAS:398001-88-2
分子式:C194H339N63O54S.XCF3COOH
分子量:4450.2
纯度:98%
存储:Store at -20°C

Background:

Urocortin II is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF , urocortin , urocortin III , frog sauvagine, and piscine urotensin I. Human urocortin II shares 34, 43, and 37-40% sequence homology with rat and human CRF, human urocortin , and human urocortin III. Urocortin II increases cell shortening and accelerates relaxation of rabbit ventricular myocytes in a time- and concentration-dependent manner. In vivo, urocortin reduces arterial blood pressure in normotensive and spontaneously hypertensive rats via peripheral CRF2 receptor agonism. It induces dose-dependent tachycardia and hypotension in rats when administered at doses of 3 and 30 pmol/kg. Urocortin (10 and 20 μg/kg) also reduces the visceral pain response to colorectal distension in conscious rats and delays gastric emptying in mice.


参考文献:
[1]. Ad?o, R., Santos-Ribeiro, D., Rademaker, M.T., et al. Urocortin 2 in cardiovascular health and disease Drug Discov. Today 20(7), 906-914 (2015).
[2]. Gardiner, S.M., March, J.E., Kemp, P.A., et al. Regional hemodynamic actions of selective corticotropin-releasing factor type 2 receptor ligands in conscious rats J. Pharmacol. Exp. Ther. 312(1), 53-60 (2005).
[3]. Million, M., Wang, L., Wang, Y., et al. CRF2 receptor activation prevents colorectal distension induced visceral pain and spinal ERK1/2 phosphorylation in rats Gut 55(2), 172-181 (2006).