ChemicalBook--->CAS DataBase List--->6674-45-9

6674-45-9

6674-45-9 Structure

6674-45-9 Structure
IdentificationBack Directory
[Name]

[[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl] [(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl hydrogen phosphate
[CAS]

6674-45-9
[Synonyms]

Diguanosine 5′-triphosphate
GP3G (Unmethylated Cap Analog)
Guanosine-5'-triphosphate-5'-Guanosine
GP3G (Unmethylated Cap Analog) - solution
[[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl] [(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl hydrogen phosphate
[Molecular Formula]

C20H27N10O18P3
[MDL Number]

MFCD34474133
[MOL File]

6674-45-9.mol
[Molecular Weight]

788.41
Chemical PropertiesBack Directory
[density ]

2.69±0.1 g/cm3(Predicted)
[pka]

0?+-.0.50(Predicted)
Hazard InformationBack Directory
[Uses]

Diguanosine 5′-triphosphate (Gp3G) is a dinucleoside triphosphates. Diguanosine 5′-triphosphate also is a virus-specific oligonucleotide. Diguanosine 5′-triphosphate is needed for the synthesis of RNA during the transcription process[1][2].
[References]

[1] M Yamakawa, et al. Priming of reovirus transcription by GppppG and formation of CpG(5')GpC. Proc Natl Acad Sci U S A. 1982 Oct;79(20):6142-6. DOI:10.1073/pnas.79.20.6142
[2] Emmanuel Klein, et al. Synthesis of enzymatically and chemically non-hydrolyzable analogues of dinucleoside triphosphates Ap(3)A and Gp(3)G. J Org Chem. 2002 Jan 11;67(1):146-53. DOI:10.1021/jo015836e
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