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(d(CH2)51,Tyr(Me)2,Arg8)-血管加压素

更新时间:2024-01-11 19:11:48

(d(CH2)51,Tyr(Me)2,Arg8)-血管加压素结构式
(d(CH2)51,Tyr(Me)2,Arg8)-血管加压素结构式
品牌特惠专场
常用名 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 英文名 (d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin trifluoroacetate salt
CAS号 73168-24-8 分子量 1151.36
密度 1.5 g/cm3 沸点 N/A
分子式 C52H74N14O12S2 熔点 N/A
MSDS 中文版 美版 闪点 N/A
符号 GHS07
GHS07
信号词 Warning

 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素用途


(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin (SKF 100273) 是一种vasopressin V1 受体选择性拮抗剂。

 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素名称

中文名 (D(CH2)51,TYR(ME)2,ARG8)-VASOPRESSIN
英文名 3-mercapto-3-methyl-butyryl-tyr(me)-phe-gln-asn-cys-pro-arg-gly-nh2
英文别名 更多

 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素生物活性

描述 (d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin (SKF 100273) 是一种vasopressin V1 受体选择性拮抗剂。
相关类别
参考文献

[1]. Arai Y, et al. New topics in vasopressin receptors and approach to novel drugs: research and development of conivaptan hydrochloride (YM087), a drug for the treatment of hyponatremia. J Pharmacol Sci. 2009 Jan;109(1):53-9.  

 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素物理化学性质

密度 1.5 g/cm3
分子式 C52H74N14O12S2
分子量 1151.36
精确质量 1150.51000
PSA 475.01000
LogP 3.52940
外观性状 白色冻干的粉末
折射率 1.695

 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素安全信息

符号 GHS07
GHS07
信号词 Warning
危害声明 H332
个人防护装备 dust mask type N95 (US);Eyeshields;Gloves
危害码 (欧洲) Xn: Harmful;
风险声明 (欧洲) R20
安全声明 (欧洲) 36
危险品运输编码 NONH for all modes of transport

 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素文献34

更多文献
Peripheral mechanisms involved in the pressor and bradycardic effects of centrally administered arachidonic acid

Prostaglandins Leukot. Essent. Fatty Acids 78(6) , 361-8, (2008)

In the current study, we aimed to determine the cardiovascular effects of arachidonic acid and peripheral mechanisms mediated these effects in normotensive conscious rats. Studies were performed in ma...

Contractile responses of human thyroid arteries to vasopressin.

Life Sci. 93(15) , 525-9, (2013)

In the present study we investigated the intervention of nitric oxide and prostacyclin in the responses to vasopressin of isolated thyroid arteries obtained from multi-organ donors.Paired artery rings...

Selective blockade of oxytocin and vasopressin V(1a) receptors in anaesthetised rats: evidence that activation of oxytocin receptors rather than V(1a) receptors increases sodium excretion.

Nephron. Exp. Nephrol. 117(3) , p21-6, (2011)

Although it is known that moderate-to-high doses of the neurohypophysial hormones oxytocin and vasopressin are natriuretic, doubts remain over the identity of the receptors responsible. To address thi...

 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素英文别名

Avpa
Aavp
MANNING COMPOUND
AVPX
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