Tenofovir Mono POC Dimer
| Product Name | Tenofovir Mono POC Dimer |
|---|---|
| CAT No. | CS-O-13571 |
| CAS No. | 1962114-92-6 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 818.67 g/mol |
| Mol. For. | C29H44N10O14P2 |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Therapeutic | Antiretroviral / Anti-HIV |
| Smileys | C[C@@H](OC[P](OCOC(OC(C)C)=O)(O)=O)CN1C2=NC=NC(NCNC3=C(N=CN4C[C@@H](C)OC[P](O)(OCOC(OC(C)C)=O)=O)C4=NC=N3)=C2N=C1 |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
Tenofovir Mono POC Dimer is a novel antiviral drug that has been developed for the treatment of HIV infection. This drug is a prodrug of tenofovir, a widely used antiretroviral drug. Tenofovir Mono POC Dimer is designed to be more effective than tenofovir by improving its bioavailability and reducing toxicity.
The chemical structure of Tenofovir Mono POC Dimer is a dimer of tenofovir monophosphate, which is the active metabolite of tenofovir. This dimer is linked by a phosphate ester bond and has a POC (propyloxy-carbonyl) group attached to the phosphate ester. The POC group serves as a prodrug moiety that facilitates the delivery of tenofovir monophosphate to the site of action.
Tenofovir Mono POC Dimer is administered orally and is rapidly absorbed into the bloodstream. Once inside the body, the POC group is cleaved by esterases, releasing tenofovir monophosphate. This active metabolite then inhibits the reverse transcriptase enzyme of HIV, preventing viral replication and reducing the viral load in the body.
Tenofovir Mono POC Dimer has been shown to be effective in reducing viral load in clinical trials. It has also been found to have a favorable safety profile, with fewer adverse effects compared to tenofovir. This drug has the potential to become an important addition to the armamentarium of antiretroviral drugs for the treatment of HIV infection.
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