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Vidarabine

SKU: orb1308405

Description

Vidarabine is a nucleoside antibiotic derived from Streptomyces antibioticus with demonstrated antineoplastic and broad-spectrum antiviral activity. It has been used in research applications, including in vitro studies against herpesviruses and in vivo models for investigating antiviral mechanisms and efficacy.

Research Area

Cell Biology, Infectious Disease & Virology, Molecular Biology, Signal Transduction

Images & Validation

Key Properties

CAS Number5536-17-4
MW267.24
Purity100.00%
FormulaC10H13N5O4
SMILESO[C@@H]1[C@H](N2C=3C(N=C2)=C(N)N=CN3)O[C@H](CO)[C@H]1O
TargetNucleoside Antimetabolite/Analog,Virus Protease,Antibiotic,Tyrosine Kinases,HSV,DNA/RNA Synthesis
Solubility10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (7.48 mM);H2O:3 mg/mL (11.23 mM);DMSO:75 mg/mL (280.65 mM);Ethanol:< 1 mg/mL (insoluble or slightly soluble)

Bioactivity

Target IC50
HSV2:11.3 μg mL IC50 |HSV1:9.3 μg mL IC50
In Vivo
Vidarabine is rapidly deaminated to 9-β-D-arabinofuranosyl hypoxanthine (Ara-Hx) a the principal metabolite.
In Vitro
Vidarabine and Acyclovir have a synergistic effect on wild type. Vidarabine is capable of inhibiting acyclovir-resistant/TK-deficient mutants of HSV and VZV, because it is phosphorylated to its active vidarabine–triphosphate form by cellular kinases and is not dependent for its activation o the viral TK. Vidarabine and acyclovir (ACV) alone show a concentration dependent Inhibition of plaque formation of HSV-1 in Vero cells. Vidarabine combined with acidic protein bound polysaccharide (APBP) show synergistic effects o the plaque formation of HSV-1 in Vero cells. Vidarabine acts directly o the DNA polymerase of varicella-zoster virus (VZV) and double-st and DNA viruses, including human adenoviruses. Vidarabine specifically inhibits adenovirus type 11 replication without obvious cytotoxicity in vitro Vidarabine acts less o the synthesis of early proteins but rather on those after DNA replication. Vidarabine is an antiviral drug with activity against herpes viruses, poxviruses, and certain rhabdoviruses, hepadnarviruses, and RNA tumor viruses. Vidarabine also is active against vaccinia virus both in vitro and in vivo

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
DisclaimerFor research use only

Alternative Names

Adenine Arabinoside, 9-b-D-Arabinofuranosyladenine, 9-beta-D-Arabinofuranosyladenine, 9-β-D-Arabinofuranosyladenine, Ara-A, Arabinosyladenine, Analog, Antibiotic, DNA polymerase, DNA Synthesis, DNASynthesis, HSV, Inhibitor, Herpes simplex virus, inhibit, Nucleoside Antimetabolite, Nucleoside Antimetabolite/Analog, NucleosideAntimetabolite, Orthopoxvirus, RNASynthesis, RNA Synthesis, Vira-A, Vidarabine, TyrosineKinases, Tyrosine Kinases

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Key Properties

No computed properties available.

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Vidarabine (orb1308405)

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% DMSO +
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% Tween 80 +
%

Available Sizes

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50 mg
$ 70.00
100 mg
$ 80.00
1 ml x 10 mM (in DMSO)
$ 90.00
500 mg
$ 140.00
1 g
$ 230.00
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