(d(CH2)51,Tyr(Me)2,Arg8)-血管加压素结构式
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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 |
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| 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 |
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。 |
| 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 |
| 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。 |
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| 相关类别 | |
| 参考文献 |
| 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 |
| InChIKey | QVQOGNOOAMQKCE-ZTYVOHGWSA-N |
| SMILES | COc1ccc(CC2NC(=O)CC3(CCCCC3)SSCC(C(=O)N3CCCC3C(=O)NC(CCCN=C(N)N)C(=O)NCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(CCC(N)=O)NC(=O)C(Cc3ccccc3)NC2=O)cc1 |
| 外观性状 | 白色冻干的粉末 |
| 折射率 | 1.695 |
| 符号 |
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 |
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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... |
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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... |
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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... |
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