CAS 160707-69-7
:Apricitabina
- (-)-2′-Deoxy-3′-oxa-4′-thiocytidine
- (-)-Bch 10652
- 1,3-Oxathiolane, 2(1H)-pyrimidinone deriv.
- 2(1H)-Pyrimidinone, 4-amino-1-[(2R,4R)-2-(hydroxymethyl)-1,3-oxathiolan-4-yl]-
- 2(1H)-Pyrimidinone, 4-amino-1-[2-(hydroxymethyl)-1,3-oxathiolan-4-yl]-, (2R-cis)-
- 4-Amino-1-[(2R,4R)-2-(hydroxymethyl)-1,3-oxathiolan-4-yl]-2(1H)-pyrimidinone
- Avx 754
- Bch 10618
- Spd 754
- APRICITABINE
- (-)-2'-Deoxy-3'-oxa-4'-thiocytidine (Apricitabine)
- Avx754
- 4-Amino-1-((2R,4R)-2-(hydroxymethyl)-1,3-oxathiolan-4-yl)pyrimidin-2(1H)-one
- Unii-K1yx059ml1
- Vedi altri sinonimi
2(1H)-Pyrimidinone, 4-amino-1-[(2R,4R)-2-(hydroxymethyl)-1,3-oxathiolan-4-yl]-
CAS:Formula:C8H11N3O3SPurezza:95%Peso molecolare:229.25624000000002Ref: IN-DA001S4O
1mg504,00€5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiesta(-)-2'-Deoxy-3'-oxa-4'-thiocytidine (Apricitabine)
CAS:Prodotto controllatoApplications (-)-2'-Deoxy-3'-oxa-4'-thiocytidine (Apricitabine) is a drug that is used in the treatment of HIV aids. It as also been shown to be useful against lamivudine and zidovudine resistant virus strains
References Sebastian M., et al.: Org. Proc. Res. & Dev., 265, 763-773 (2011) Ghosh, R., et al.: Expert Opin. Pharmacother., 12, 31-46 (2011)Formula:C8H11N3O3SColore e forma:NeatPeso molecolare:229.25Apricitabine
CAS:Apricitabine (SPD754) is a highly selective and orally active HIV-1 reverse transcriptase inhibitor (Ki=0.08 μM), the (-) enantiomer of 2′-deoxy-3′-oxy-4′-Formula:C8H11N3O3SPurezza:99.45%Colore e forma:SolidPeso molecolare:229.26Ref: TM-T14313
1mg283,00€5mg507,00€10mg628,00€25mg962,00€50mg1.601,00€100mg2.682,00€1mL*10mM (DMSO)592,00€(-)-2'-Deoxy-3'-oxa-4'-thiocytidine (apricitabine)
CAS:Apricitabine is a nucleoside analog that has been shown to be active against HIV. It inhibits HIV-1 reverse transcriptase by competing with the natural substrate, deoxycytidine triphosphate, and thereby prevents RNA synthesis. Apricitabine can be used for treatment of chronic hepatitis B or C virus infections, as well as long-term therapy for HIV infection. The drug has shown long-term efficacy in reducing viral load in patients receiving antiretroviral therapy, without causing significant toxicity. Apricitabine is not metabolized by cytochrome P450 enzymes and does not have significant interactions with other drugs. The drug binds to DNA in the cell nucleus and inhibits the process of DNA replication. The clinical use of apricitabine is limited by its short half-life (approximately 1 hour), which requires intravenous administration twice daily.
Formula:C8H11N3O3SPurezza:Min. 95%Peso molecolare:229.26 g/mol




