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
Melting point	250 °C (482 °F; 523 K)
	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 purine nucleobase guanine linked by its N9 nitrogen to the C1 carbon of deoxyribose. It is similar to guanosine, but with one 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)".

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