Deoxyguanosine

Deoxyguanosine
	Ball-and-stick model of the deoxyadenosine molecule
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
ChEBI	CHEBI:17172
ChEMBL	ChEMBL68908
ChemSpider	163230
Jmol 3D model	Interactive image
MeSH	Deoxyguanosine
PubChem	638
	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	267.24 g/mol
Vapor pressure	{{{value}}}
	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.

See also