2305416-07-1
![N2-[(N,N-Dimethyl amino]methylene-N1-methyl-2’-O-methylguanosine Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-152547.gif "N2-[(N,N-Dimethyl amino]methylene-N1-methyl-2’-O-methylguanosine Chemical Structure")
Chemical Structure
N2-[(N,N-Dimethyl amino]methylene-N1-methyl-2’-O-methylguanosine
- CAS No.: 2305416-07-1
- Formula:C15H22N6O5
- Molecular Weight:366.37
IUPAC Name: (E)-N'-(9-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)-1-methyl-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethylformimidamide
InChIKey: LOSZXLFNDXRZQH-QKKNGTDUSA-N
SMILES: O=C1N(C)C(/N=C/N(C)C)=NC2=C1N=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3OC
Biological Activity: N2-[(N,N-Dimethyl amino]methylene-N1-methyl-2’-O-methylguanosine is a guanosine analog. Some guanosine analogs have immunostimulatory activity. In some animal models, they also induce type I interferons, producing antiviral effects. Studies have shown that the functional activity of guanosine analogs is dependent on the activation of Toll-like receptor 7 (TLR7)[1].
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N2-[(N,N-Dimethyl amino]methylene-N1-methyl-2’-O-methylguanosine | N2-[(N,N-Dimethyl amino]methylene-N1-methyl-2’-O-methylguanosine is a guanosine analog. Some guanosine analogs have immunostimulatory activity. In some animal models, they also induce type I interferons, producing antiviral effects. Studies have shown that the functional activity of guanosine analogs is dependent on the activation of Toll-like receptor 7 (TLR7). | |||||||||||||||||||||
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