Home Categories Biochemical Engineering 2′-Fluoro-2′-deoxycytidine
A4327212

2′-Fluoro-2′-deoxycytidine , >98.0%(T) , 10212-20-1

CAS NO.:10212-20-1

Empirical Formula: C9H12FN3O4

Molecular Weight: 245.21

MDL number: MFCD00057445

EINECS: 1806241-263-5

Pack Size Price Stock Quantity
1G RMB190.40 In Stock
5G RMB719.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 167 °C
Boiling point: 500.1±60.0 °C(Predicted)
Density  1.82±0.1 g/cm3(Predicted)
refractive index  80 ° (C=1, MeOH)
storage temp.  Keep in dark place,Sealed in dry,2-8°C
solubility  Soluble in DMSO, Methanol.
pka 12.84±0.70(Predicted)
form  Powder
color  White to Off-white
Water Solubility  Water: 5 mg/mL (20.39 mM; ultrasonic and warming and heat to 60°C)
InChI InChI=1S/C9H12FN3O4/c10-6-7(15)4(3-14)17-8(6)13-2-1-5(11)12-9(13)16/h1-2,4,6-8,14-15H,3H2,(H2,11,12,16)/t4-,6-,7-,8-/m1/s1
InChIKey NVZFZMCNALTPBY-XVFCMESISA-N
SMILES OC[C@H]1O[C@@H](N2C=CC(N)=NC2=O)[C@H](F)[C@@H]1O
CAS DataBase Reference 10212-20-1(CAS DataBase Reference)

Description and Uses

2'-Deoxy-2'-fluorocytidine is a nucleoside analog. It has antiviral effects and can synergize with T705 to effectively inhibit Crimean-Congo hemorrhagic fever virus (CCHFV) replication. 2'-Deoxy-2'-fluorocytidine can also inhibit dihydrofolate reductase, thereby preventing the production of tetrahydrofolate, which is required for the synthesis of purines and pyrimidines. It has a certain inhibitory effect on poliovirus, herpes simplex virus, vesicular stomatitis virus and influenza A virus.

2'-Deoxy-2'-fluorocytidine is a potent inhibitor of the subgenomic hepatitis C virus replicon in Huh-7 cells. 2'-Deoxy-2'-fluorocytidine has been shown to inhibit Borna Disease virus replication and s pread.

Safety

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
HS Code  29389090

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