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Invopressin
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Catalog No. T80270Cas No. 1488411-60-4
Alias OCE-205
Invopressin (Compound 42), a vasopressin V1A receptor partial agonist (EC50: 1.0 nM), is utilized in research related to cirrhosis conditions such as bacterial peritonitis, HRS2, and refractory ascites [1].
Invopressin
😃Good
Catalog No. T80270Alias OCE-205Cas No. 1488411-60-4
Invopressin (Compound 42), a vasopressin V1A receptor partial agonist (EC50: 1.0 nM), is utilized in research related to cirrhosis conditions such as bacterial peritonitis, HRS2, and refractory ascites [1].
| Pack Size | Price | Availability | Quantity |
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| 50 mg | Inquiry | Backorder |
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Atosiban acetate
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Terlipressin Acetate
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Conopressin S acetate(111317-90-9 free base)
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Product Introduction
Bioactivity
Chemical Properties
| Description | Invopressin (Compound 42), a vasopressin V1A receptor partial agonist (EC50: 1.0 nM), is utilized in research related to cirrhosis conditions such as bacterial peritonitis, HRS2, and refractory ascites [1]. |
| Alias | OCE-205 |
| Molecular Weight | 2413.78 |
| Formula | C110H161N31O27S2 |
| Cas No. | 1488411-60-4 |
Storage & Solubility Information
| Storage | keep away from moisture | Shipping with blue ice. |
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DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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