2'-C-Methylcytidine

Description

2'-C-Methylcytidine is a nucleoside analog with antiviral properties. It has shown be a potent replication inhibitor, in vivo, towards multiple RNA viruses including hepatitus C virus (HCV). 2'-C-Methylcytidine has been shown inhibit viral RNA polymerase, disrupting replicon formation and preventing viral proliferation. While 2'-C-Methycytidine is a strong antiviral, it has exhibited low oral bioavailability.

Product Specifications
2'-C-Methylcytidine
NM-107

Formula: C10H15N3O5

MW: 257.24 g/mol

Storage/Handling: Store desiccated at -20°C.

PubChem Chemical ID: 500902

NOT FOR HUMAN USE!!

2'-C-Methylcytidine

View Sizes & Pricing

Catalog Number:
M-315-10
CAS Number:
20724-73-6
$162.00

For research use only. Not for food, drug, household, or cosmetic use.
Availability:
2-3 Weeks
Shipping:
$14.99 Ground shipping (In continental US only.)

    Description

    2'-C-Methylcytidine is a nucleoside analog with antiviral properties. It has shown be a potent replication inhibitor, in vivo, towards multiple RNA viruses including hepatitus C virus (HCV). 2'-C-Methylcytidine has been shown inhibit viral RNA polymerase, disrupting replicon formation and preventing viral proliferation. While 2'-C-Methycytidine is a strong antiviral, it has exhibited low oral bioavailability.

    Product Specifications
    2'-C-Methylcytidine
    NM-107

    Formula: C10H15N3O5

    MW: 257.24 g/mol

    Storage/Handling: Store desiccated at -20°C.

    PubChem Chemical ID: 500902

    NOT FOR HUMAN USE!!

    Product Specifications

    Catalog ID: M-315
    CAS #: 20724-73-6
    Formula: C10H15N3O5
    MW: 257.24 g/mol
    Storage/handling: Store desiccated at -20°C.
    PubChem Chemical ID: 500902
    IUPAC Name: 4-amino-1-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-3-methyloxolan-2-yl]pyrimidin-2-one
    InChI: InChI=1S/C10H15N3O5/c1-10(17)7(15)5(4-14)18-8(10)13-3-2-6(11)12-9(13)16/h2-3,5,7-8,14-15,17H,4H2,1H3,(H2,11,12,16)/t5-,7-,8-,10-/m1/s1
    InChIKey: PPUDLEUZKVJXSZ-VPCXQMTMSA-N
    SMILES: CC1(C(C(OC1N2C=CC(=NC2=O)N)CO)O)O

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