Navuridine
CAS No. 84472-85-5
Navuridine( AZdU | AzUrd | CS-87 | 3'-Azido-2',3'-dideoxyuridine | CS 87 | AZddU )
Catalog No. M27413 CAS No. 84472-85-5
Navuridine is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.
Navuridine is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 61 | Get Quote |
|
10MG | 106 | Get Quote |
|
25MG | 222 | Get Quote |
|
50MG | 353 | Get Quote |
|
100MG | 533 | Get Quote |
|
500MG | 1152 | Get Quote |
|
1G | Get Quote | Get Quote |
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Biological Information
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Product NameNavuridine
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NoteResearch use only, not for human use.
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Brief DescriptionNavuridine is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.
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DescriptionNavuridine is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.
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In Vitro
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In VivoPharmacokinetic Parameters of 3′-Azido-2′,3′-dideoxyuridine in male Sprague-Dawley rats. Animal Model:Adult male Sprague-Dawley rats (300-400 g)Dosage:25, 100 mg/kg Administration:Intravenous bolus injection or oral gavage (Pharmacokinetic Analysis)Result:The oral bioavailability estimates of 3′-Azido-2′,3′-dideoxyuridine at doses of 25 and 100 mg/kg averaged 53%.
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SynonymsAZdU | AzUrd | CS-87 | 3'-Azido-2',3'-dideoxyuridine | CS 87 | AZddU
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PathwayMicrobiology/Virology
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TargetHIV
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Recptor
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Research Area
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Indication
Chemical Information
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CAS Number84472-85-5
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Formula Weight253.218
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Molecular FormulaC9H11N5O4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (987.32 mM)
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SMILESOC[C@H]1O[C@H](C[C@@H]1N=[N+]=[N-])n1ccc(=O)[nH]c1=O
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Chemical Name
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Fang Liu, et al. N-3-oxo-octanoyl-homoserine lactone-mediated priming of resistance to Pseudomonas syringae requires the salicylic acid signaling pathway in Arabidopsis thaliana. BMC Plant Biol. 2020 Jan 28;20(1):38.
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