(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin trifluoroacetate salt structure
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Common Name | (d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin trifluoroacetate salt | ||
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| CAS Number | 73168-24-8 | Molecular Weight | 1151.36 | |
| Density | 1.5 g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C52H74N14O12S2 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of (d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin trifluoroacetate salt(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin (SKF 100273) is a vasopressin V1 receptor selective antagonist[1]. |
| Name | 3-mercapto-3-methyl-butyryl-tyr(me)-phe-gln-asn-cys-pro-arg-gly-nh2 |
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| Synonym | More Synonyms |
| Description | (d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin (SKF 100273) is a vasopressin V1 receptor selective antagonist[1]. |
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| Related Catalog | |
| References |
| Density | 1.5 g/cm3 |
|---|---|
| Molecular Formula | C52H74N14O12S2 |
| Molecular Weight | 1151.36 |
| Exact Mass | 1150.51000 |
| PSA | 475.01000 |
| LogP | 3.52940 |
| Index of Refraction | 1.695 |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H332 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xn: Harmful; |
| Risk Phrases | R20 |
| Safety Phrases | 36 |
| RIDADR | 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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