MedKoo Cat#: 525733 | Name: Navuridine
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Navuridine, also known as 3’-Azido-2’,3’-dideoxyuridine, is a dideoxyuridine inhibitor of HIV reverse transcriptase that is related to zidovudine. Navuridine exhibits a relatively short half-life and incomplete oral bioavailability and has not been developed into a clinical drug.

Chemical Structure

Navuridine
Navuridine
CAS#84472-85-5

Theoretical Analysis

MedKoo Cat#: 525733

Name: Navuridine

CAS#: 84472-85-5

Chemical Formula: C9H11N5O4

Exact Mass: 253.0811

Molecular Weight: 253.22

Elemental Analysis: C, 42.69; H, 4.38; N, 27.66; O, 25.27

Price and Availability

Size Price Availability Quantity
10mg USD 350.00 2 Weeks
200mg USD 2,850.00 2 Weeks
500mg USD 3,950.00 2 Weeks
1g USD 4,850.00 2 Weeks
2g USD 6,650.00 2 Weeks
5g USD 12,650.00 2 Weeks
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Related CAS #
No Data
Synonym
AZdU; AzUrd; CS-87; CS87; CS 87; AZddU; NSC 380882; NSC380882; NSC-380882; Navuridine, 3’-Azido-2’,3’-dideoxyuridine
IUPAC/Chemical Name
1-((2R,4S,5S)-4-azido-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
InChi Key
ZSNNBSPEFVIUDS-SHYZEUOFSA-N
InChi Code
InChI=1S/C9H11N5O4/c10-13-12-5-3-8(18-6(5)4-15)14-2-1-7(16)11-9(14)17/h1-2,5-6,8,15H,3-4H2,(H,11,16,17)/t5-,6+,8+/m0/s1
SMILES Code
O=C1NC(C=CN1[C@@H]2O[C@H](CO)[C@@H](N=[N+]=[N-])C2)=O
Appearance
Solid powder
Purity
>95% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO, not in water
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Biological target:
Navuridine is a dideoxyuridine inhibitor of HIV reverse transcriptase.
In vitro activity:
TBD
In vivo activity:
TBD
Solvent mg/mL mM
Solubility
DMF 2.0 7.90
DMSO 126.0 497.59
PBS (pH 7.2) 1.0 3.95
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 253.22 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
TBD
In vitro protocol:
TBD
In vivo protocol:
TBD