2'-C-Methylcytidine

Modify Date: 2024-01-02 22:59:04

2'-C-Methylcytidine Structure
2'-C-Methylcytidine structure
Common Name 2'-C-Methylcytidine
CAS Number 20724-73-6 Molecular Weight 257.243
Density 1.7±0.1 g/cm3 Boiling Point 523.9±60.0 °C at 760 mmHg
Molecular Formula C10H15N3O5 Melting Point 243-245ºC
MSDS Chinese USA Flash Point 270.7±32.9 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 2'-C-Methylcytidine


NM107 is a inhibitors of HCV RNA replication with IC50 of 7.0 μM in vitro.IC50 value: 7.0 μMTarget:HCV RNA replicationNM107 is a potent and selective inhibitor of flavi- and pesti-virus replication in cell culture, with inhibitory activity and cytotoxicity against HCV 1b replicon cells, IC50 is 1.13 μM. Intracellular HCV RNA in HCV-infected cells treated the HCV polymerase inhibitor NM107 shows a similar pattern of decline. NM107 are currently being investigated as additional therapeutic agents for HCV infection. NM107 inhibits bovine viral diarrhea virus (BVDV) replication (EC50 0.67 nM), eliminates persistent BVDV infection at nontoxic concentrations.

 Names

Name 4-amino-1-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-3-methyloxolan-2-yl]pyrimidin-2-one
Synonym More Synonyms

 2'-C-Methylcytidine Biological Activity

Description NM107 is a inhibitors of HCV RNA replication with IC50 of 7.0 μM in vitro.IC50 value: 7.0 μMTarget:HCV RNA replicationNM107 is a potent and selective inhibitor of flavi- and pesti-virus replication in cell culture, with inhibitory activity and cytotoxicity against HCV 1b replicon cells, IC50 is 1.13 μM. Intracellular HCV RNA in HCV-infected cells treated the HCV polymerase inhibitor NM107 shows a similar pattern of decline. NM107 are currently being investigated as additional therapeutic agents for HCV infection. NM107 inhibits bovine viral diarrhea virus (BVDV) replication (EC50 0.67 nM), eliminates persistent BVDV infection at nontoxic concentrations.
Related Catalog
References

[1]. McCown MF, et al. The hepatitis C virus replicon presents a higher barrier to resistance to nucleoside analogs than to nonnucleosidepolymerase or protease inhibitors. Antimicrob Agents Chemother. 2008 May;52(5):1604-1612.

 Chemical & Physical Properties

Density 1.7±0.1 g/cm3
Boiling Point 523.9±60.0 °C at 760 mmHg
Melting Point 243-245ºC
Molecular Formula C10H15N3O5
Molecular Weight 257.243
Flash Point 270.7±32.9 °C
Exact Mass 257.101166
PSA 130.83000
LogP -0.80
Vapour Pressure 0.0±3.1 mmHg at 25°C
Index of Refraction 1.700
Storage condition Hygroscopic, -20°C Freezer, Under Inert Atmosphere
Water Solubility H2O: >20mg/mL

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Hazard Codes Xi
Risk Phrases 36/37/38
Safety Phrases 26
RIDADR NONH for all modes of transport
HS Code 2934999090

 Synthetic Route

 Customs

HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Synonyms

valopicitabine
2-C-METHYLCYTIDINE
2'-C-Methyl Cytidine
Cytidine,2'-C-methyl
2'-METHYLCYTIDINE
NM107
Cytidine, 2'-C-methyl-
UNII-27FS20C1D8
1-((2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)-4-aminopyrimidin-2(1H)-one
UNII:27FS20C1D8
2'-C-methylcytidine
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