Home > Signaling Pathways>Anti-infection>HIV>Apricitabine [(-)-BCH10652; (-)-dOTC; AVX754; BCH10618; SPD754]
Apricitabine [(-)-BCH10652; (-)-dOTC; AVX754; BCH10618; SPD754]

This product is for research use only, not for human use. We do not sell to patients.

Apricitabine [(-)-BCH10652; (-)-dOTC; AVX754; BCH10618; SPD754]
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Cat #: V8732 CAS #: 160707-69-7 Purity ≥ 99%

Description: Apricitabine [(-)-BCH-10652; (-)-dOTC; AVX-754; BCH-10618; SPD-754] is a highly potent, selective and orally bioactive HIV-1 reverse transcriptase (RT) inhibitor with Ki of 0.08 μM, belonging to the nucleoside reverse transcriptase inhibitor (NRTI) class of anti-HIV agents.

References: de Muys JM, et al. Anti-human immunodeficiency virus type 1 activity, intracellular metabolism, and pharmacokinetic evaluation of 2'-deoxy-3'-oxa-4'-thiocytidine.Antimicrob Agents Chemother. 1999 Aug;43(8):1835-44.

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Molecular Weight (MW)229.26
Molecular FormulaC8H11N3O3S
CAS No.160707-69-7
SMILES Code O=C1N=C(N)C=CN1[C@@H]2S[C@H](CO)OC2
Synonyms(-)-BCH10652; AVX754; BCH10618; SPD754; Apricitabine; (-)-BCH-10652; (-)-dOTC; AVX-754; BCH-10618; SPD-754;
ProtocolIn VitroApricitabine (SPD754; AVX754) is against clinical isolates of HIV-1 in cultured PBMCs with IC50 values of 0.2 μM, 1.45 μM, 2.2 μM and 2.4 μM for HIV-1RF, Wild type, 3TC resistant, 3TC and AZT resistant, respectively.
In VivoApricitabine (SPD754; AVX754) (oral adminstation; 10 mg/kg; once a day) exhibits a good oral bioavailability of 68% for males and 69.4% for females rats. And the T1/2, AUC0–∞, Tmax, Cmax are 62.2 mins, 157.4 μg/min/ml and 37.3 mins, 1.16 μg/ml in female rats.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM4.3619 mL21.8093 mL43.6186 mL87.2372 mL
5mM0.8724 mL4.3619 mL8.7237 mL17.4474 mL
10mM0.4362 mL2.1809 mL4.3619 mL8.7237 mL
20mM0.2181 mL1.0905 mL2.1809 mL4.3619 mL
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
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Concentration
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Volume
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Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

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Concentration(final)
C2
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Volume(final)
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Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

Calculation Results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in µL DMSO(Master liquid concentration mg/mL) ,Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation: Take µL DMSO master liquid, next add µL PEG300, mix and clarify, next add µL Tween 80,mix and clarify, next add µL ddH2O,mix and clarify.
Note:
  • (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
  • (2) Be sure to add the solvent(s) in order.