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Opaviraline
🥰Excellent
Catalog No. T28255Cas No. 178040-94-3
Alias HBY-1293, GW-867, GW867, GW-420867X, GW420867X
Opaviraline (GW-420867X) is a potent reverse transcriptase inhibitor that inhibits Human immunodeficiency virus 1 and has the potential to treat HIV infection.
Opaviraline
🥰Excellent
Purity: 100%
Catalog No. T28255Alias HBY-1293, GW-867, GW867, GW-420867X, GW420867XCas No. 178040-94-3
Opaviraline (GW-420867X) is a potent reverse transcriptase inhibitor that inhibits Human immunodeficiency virus 1 and has the potential to treat HIV infection.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $397 | In Stock | |
| 5 mg | $970 | In Stock | |
| 10 mg | $1,290 | In Stock | |
| 25 mg | $1,950 | In Stock | |
| 50 mg | $2,620 | In Stock | |
| 100 mg | $3,530 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $867 | In Stock |
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CitedSelect Batch
Purity:100%
ee:97.04%
Contact us for more batch information
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | Opaviraline (GW-420867X) is a potent reverse transcriptase inhibitor that inhibits Human immunodeficiency virus 1 and has the potential to treat HIV infection. |
| In vivo | systemic exposure to Opaviraline decreases with increasing dose and displays time-variant pharmacokinetics, which suggests decreased absorption and/or increased clearance of Opaviraline. With an approximately 50-hour plasma half-life, Opaviraline is well-suited for once-daily dosing due to its relatively prolonged duration of action.[1] |
| Alias | HBY-1293, GW-867, GW867, GW-420867X, GW420867X |
| Molecular Weight | 280.29 |
| Formula | C14H17FN2O3 |
| Cas No. | 178040-94-3 |
| Smiles | C(OC(C)C)(=O)N1C=2C(NC(=O)[C@@H]1CC)=CC=C(F)C2 |
| Relative Density. | 1.204g/cm3 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||
| Solubility Information | DMSO: 10 mg/mL (35.68 mM)  | |||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||
DMSO
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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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