
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.
Purity : >98% (HPLC)






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 |
![]() ![]() |
Biological Information
-
Product NameNavuridine
-
NoteResearch use only, not for human use.
-
Brief DescriptionNavuridine is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.
-
DescriptionNavuridine is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.
-
In Vitro——
-
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%.
-
SynonymsAZdU | AzUrd | CS-87 | 3'-Azido-2',3'-dideoxyuridine | CS 87 | AZddU
-
PathwayMicrobiology/Virology
-
TargetHIV
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number84472-85-5
-
Formula Weight253.218
-
Molecular FormulaC9H11N5O4
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 250 mg/mL (987.32 mM)
-
SMILESOC[C@H]1O[C@H](C[C@@H]1N=[N+]=[N-])n1ccc(=O)[nH]c1=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
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.
molnova catalog



related products
-
GS-9822
GS-9822 is a potent, non-catalytic site HIV integrase inhibitor with wild type EC50 of 3 nM.
-
Saquinavir
Apotent and selective inhibitor of HIV-1 protease with IC50 of 0.5-6 nM in cell assays.
-
(2RS)-FPMPA
(2RS)-FPMPA(FPMPA) has antiviral activity with an IC50 value of 1.85 μM measured in human MT12 cells infected with SHIV (DH4R).