Deoxyguanosine

Deoxyguanosine
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^Y
3D model (Jmol)	Interactive image
ChEBI	CHEBI:17172^N
ChEMBL	ChEMBL68908^N
ChemSpider	163230^Y
ECHA InfoCard	100.012.278
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^Y Key: YKBGVTZYEHREMT-KVQBGUIXSA-N^Y 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
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
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