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(R)-Vorbipiprant
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Catalog No. T88706Cas No. 2502965-92-4
Alias (R)-CR6086
(R)-Vorbipiprant ((R)-CR6086) is an orally effective antagonist of the prostaglandin E2 receptor 4 (EP4), demonstrating a Ki of 16.6 nM for human EP4. It inhibits the production of cAMP induced by PGE2, with an IC50 of 22 nM. Additionally, (R)-Vorbipiprant exhibits immunomodulatory and antiangiogenic activities, having shown potential to alleviate collagen-induced arthritis in mice.
(R)-Vorbipiprant
😃Good
Catalog No. T88706Alias (R)-CR6086Cas No. 2502965-92-4
(R)-Vorbipiprant ((R)-CR6086) is an orally effective antagonist of the prostaglandin E2 receptor 4 (EP4), demonstrating a Ki of 16.6 nM for human EP4. It inhibits the production of cAMP induced by PGE2, with an IC50 of 22 nM. Additionally, (R)-Vorbipiprant exhibits immunomodulatory and antiangiogenic activities, having shown potential to alleviate collagen-induced arthritis in mice.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks |
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Product Introduction
Bioactivity
Chemical Properties
| Description | (R)-Vorbipiprant ((R)-CR6086) is an orally effective antagonist of the prostaglandin E2 receptor 4 (EP4), demonstrating a Ki of 16.6 nM for human EP4. It inhibits the production of cAMP induced by PGE2, with an IC50 of 22 nM. Additionally, (R)-Vorbipiprant exhibits immunomodulatory and antiangiogenic activities, having shown potential to alleviate collagen-induced arthritis in mice. |
| Targets&IC50 | hEP4:16.6 nM (Ki) |
| Alias | (R)-CR6086 |
| Molecular Weight | 472.5 |
| Formula | C26H27F3N2O3 |
| Cas No. | 2502965-92-4 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
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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