Valopicitabine dihydrochloride

Modify Date: 2024-01-12 12:43:06

Valopicitabine dihydrochloride Structure
Valopicitabine dihydrochloride structure
Common Name Valopicitabine dihydrochloride
CAS Number 640725-71-9 Molecular Weight 429.30
Density N/A Boiling Point N/A
Molecular Formula C15H26Cl2N4O6 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Valopicitabine dihydrochloride


Valopicitabine (NM283) dihydrochloride is a nucleoside analog and the orally bioavailable prodrug of the potent anti-HCV agent 2'-C-methylcytidine (NM107). NM107competitively inhibits NS5B polymerase, causing chain termination[1][2].

 Names

Name [(2R,3R,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-4-hydroxy-2-(hydroxymethyl)-4-methyloxolan-3-yl] (2S)-2-amino-3-methylbutanoate,dihydrochloride
Synonym More Synonyms

 Valopicitabine dihydrochloride Biological Activity

Description Valopicitabine (NM283) dihydrochloride is a nucleoside analog and the orally bioavailable prodrug of the potent anti-HCV agent 2'-C-methylcytidine (NM107). NM107competitively inhibits NS5B polymerase, causing chain termination[1][2].
Related Catalog
In Vivo Valopicitabine (NM283) (100 mg/kg; oral administration; Sprague-Dawley Rats) dihydrochloride shows the Cmax, AUC, t1/2, and tmax were 3.624 μg/mL, 8.95 μg h/mL, 0.64 hours and 1 hour, respectively[2].
References

[1]. Liu-Young G, et al. Hepatitis C protease and polymerase inhibitors in development. AIDS Patient Care STDS. 2008;22(6):449-457.

[2]. Pierra C, et al. Synthesis and pharmacokinetics of valopicitabine (NM283), an efficient prodrug of the potent anti-HCV agent 2'-C-methylcytidine. J Med Chem. 2006;49(22):6614-6620.

 Chemical & Physical Properties

Molecular Formula C15H26Cl2N4O6
Molecular Weight 429.30
Exact Mass 428.12300
PSA 163.91000
LogP 1.00800

 Synonyms

Valopicitabine dihydrochloride
NM283
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