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Apricitabine (Synonyms: AVX754, BCH 10618, (–)-BCH 10652, (–)-dOTC, SPD-754)

Catalog No.GC49776

L'apricitabine (SPD754; AVX754), l'énantiomère (-) de la 2′-désoxy-3′-oxa-4′-thiocytidine (dOTC), est un inhibiteur de la transcriptase inverse (RT) du VIH-1 hautement sélectif et actif par voie orale (Ki= 0,08 μM), ainsi qu'inhibe les ADN polymérases α, β et γ avec une valeur Ki de 300 μM, 12 μM et 112,25 μM, respectivement .

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Apricitabine Chemical Structure

Cas No.: 160707-69-7

Taille Prix Stock Qté
5 mg
71,00 $US
En stock
10 mg
136,00 $US
En stock
25 mg
303,00 $US
En stock
50 mg
571,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

Apricitabine is a nucleoside reverse transcriptase inhibitor (NRTI) and derivative of 2’-deoxycytidine .1 It is phosphorylated intracellularly to its active form, apricitabine-5’-triphosphate, which competes with a monophosphate form for binding to HIV-1 reverse transcriptase and incorporation into the nascent viral DNA, inducing chain termination and HIV-1 replication. Apricitabine reduces HIV-1 infectivity in MT-4 and U937 cells (IC50s = 2.8 and 0.4 µM, respectively), as well as in isolated human cord blood mononuclear cells (CBMCs; IC50 = 0.4 µM).2

1.Cox, S., and Southby, J.Apricitabine--a novel nucleoside reverse transcriptase inhibitor for the treatment of HIV infection that is refractory to existing drugsExpert Opin. Investig. Drugs18(2)199-209(2009) 2.Mansour, T.S., Jin, H., Wang, W., et al.Structure-activity relationships among a new class of antiviral heterosubstituted 2′,3′-dideoxynucleoside analoguesNucleos. Nucleot.14(3-5)627-635(1995)

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Average Rating: 5 ★★★★★ (Based on Reviews and 7 reference(s) in Google Scholar.)

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