Deoxyguanosine

Deoxyguanosine^[1]
Names
	IUPAC name 2-Amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one
Identifiers
CAS Number	961-07-9 ;
3D model ( JSmol)	Interactive image;
ChEBI	CHEBI:17172 ;
ChEMBL	ChEMBL68908 ;
ChemSpider	163230 ;
ECHA InfoCard	100.012.278
MeSH	Deoxyguanosine
PubChem CID	638;
UNII	G9481N71RO ;
CompTox Dashboard (EPA)	DTXSID30883626 ;
	InChI InChI=1S/C10H13N5O4/c11-10-13-8-7(9(18)14-10)12-3-15(8)6-1-4(17)5(2-16)19-6/h3-6,16-17H,1-2H2,(H3,11,13,14,18)/t4-,5+,6+/m0/s1 Key: YKBGVTZYEHREMT-KVQBGUIXSA-N ; InChI=1/C10H13N5O4/c11-10-13-8-7(9(18)14-10)12-3-15(8)6-1-4(17)5(2-16)19-6/h3-6,16-17H,1-2H2,(H3,11,13,14,18)/t4-,5+,6+/m0/s1 Key: YKBGVTZYEHREMT-KVQBGUIXBI;
	SMILES c1nc2c(n1[C@H]3C[C@@H]([C@H](O3)CO)O)[nH]c(nc2=O)N;
Properties
Chemical formula	C10H13N5O4
Molar mass	267.245 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Deoxyguanosine is composed of the

hydroxyl group removed from the 2' position of the ribose sugar (making it deoxyribose). If a phosphate group is attached at the 5' position, it becomes deoxyguanosine monophosphate

.

Deoxyguanosine is one of the four

deoxyribonucleosides that make up DNA.^[2]

References

^ "2'-deoxyguanosine". PubChem Compound Database. National Center for Biotechnology Information. 24 December 2016. Archived from the original on 2 January 2017. Retrieved 2 January 2017.
^ "Human Metabolome Database (HMDB) metabocard for Deoxyguanosine (HMDB0000085)".

This biochemistry article is a stub. You can help Wikipedia by expanding it.

[pubchem_2'-1] "2'-deoxyguanosine". PubChem Compound Database. National Center for Biotechnology Information. 24 December 2016. Archived from the original on 2 January 2017. Retrieved 2 January 2017.

[2] "Human Metabolome Database (HMDB) metabocard for Deoxyguanosine (HMDB0000085)".

[1]

[2]

See also

References