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2'-deoxy-2'-fluoro-2'-C-methyluridine

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2'-deoxy-2'-fluoro-2'-C-methyluridine Basic information

Product Name:
2'-deoxy-2'-fluoro-2'-C-methyluridine
Synonyms:
  • 2'-deoxy-2'-fluoro-2'-C-methyluridine
  • 2'-Deoxy-2-floro-2'Methyl-uridine
  • 1-((2S,3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxyMethyl)-3-Methyltetrahydrofuran-2-yl)pyriMidine-2,4(1H,3H)-dione
  • 1-((2R,3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxyMethyl)-3-Methyltetrahydrofuran-2-yl)pyriMidine-2,4(1H,3H)-dione
  • PSI-6206
  • RO 2433
  • Uridine, 2'-deoxy-2'-fluoro-2'-Methyl-, (2'R)-
  • Uridine, 2'-deoxy-2'-fluoro-2'-Methyl-, (2'R)- PSI6206
CAS:
863329-66-2
MF:
C10H13FN2O5
MW:
260.22
EINECS:
810-481-6
Product Categories:
  • Sofosbuvir intermediate
  • Inhibitor
  • apis
  • Inhibitors
Mol File:
863329-66-2.mol
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2'-deoxy-2'-fluoro-2'-C-methyluridine Chemical Properties

Melting point:
237-238℃
Density 
1.55
storage temp. 
Sealed in dry,Store in freezer, under -20°C
solubility 
DMSO (Slightly), Methanol (Slightly, Heated)
pka
9.39±0.10(Predicted)
form 
Solid
color 
White to Light Beige
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Safety Information

HS Code 
2934.99.4400
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2'-deoxy-2'-fluoro-2'-C-methyluridine Usage And Synthesis

Description

(2'R)-2'-Deoxy-2'-fluoro-2'-methyluridine / PSI-6206 is the deaminated metabolite of β-D-2'-Deoxy-2'-fluoro-2'-C-methylcytidine, an effective inhibitor of hepatitis C virus (HCV) RNA polymerase.

Uses

RO 2433 is the deaminated metabolite of β-D-2''-Deoxy-2''-fluoro-2''-C-methylcytidine, an effective inhibitor of hepatitis C virus (HCV) replication in vitro.

Biological Activity

psi-6206 (as known as ro-2433 or gs-331007), β-d-2’-deoxy-2’-fluoro-2’-c-methyluridine, is the deaminated derivative of psi-6130, β-d-2’-deoxy-2’-fluoro-2’-c-methylcytidine, which is a potent inhibitor of hepatitis c virus (hcv) replication in the subgenomic hcv reolicon system. psi-6206, itself, does not shown any inhibitory activity towards hcv replication in the hcv subgenomic replicon system. however, the its triphosphate form, ro2433-tp, is a potent inhibitor of rna synthesis by hcv polymerase, which inhibits both the rna sysnthesis activity of hcv replicase (ic50 = 1.19 um) and the rna synthesis activity of the recombinant hcv con1 ns58 on a heteropolymeric rna template derived from the 3’-end of the negative strand of the hcv genome (ic50 = 0.52 um and ki = 0.141 um).han ma, wen-rong jiang, nicole robledo, vincent leveque, samir ali, teresa lara-jamie, mohammad masjedizadeh, david b. smith, nick cammack, klaus klumpp, and julian symons. characterization of the metabolic ctivation of hepatitis c virus nucleoside inhibitor β-d-2’-deoxy-2’-fluoro-2’-c-methylcytidine (psi-6130) and identification of a novel active 5’-triphosphate species. the journal of biological chemistry 2007; 282(41): 29812-29820

target

HCV

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