Deoxyadenosine

Deoxyadenosine

Identifiers
CAS number	958-09-8^Y
PubChem	636
ChemSpider	13135^Y
UNII	P582C98ULC^Y
MeSH	2'-deoxyadenosine
ChEBI	CHEBI:17256^Y
ChEMBL	CHEMBL416340^N
Jmol-3D images	Image 1
SMILES n2c1c(ncnc1n(c2)[C@@H]3O[C@@H]([C@@H](O)C3)CO)N
InChI InChI=1S/C10H13N5O3/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(17)6(2-16)18-7/h3-7,16-17H,1-2H2,(H2,11,12,13)/t5-,6+,7+/m0/s1^Y Key: OLXZPDWKRNYJJZ-RRKCRQDMSA-N^Y InChI=1/C10H13N5O3/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(17)6(2-16)18-7/h3-7,16-17H,1-2H2,(H2,11,12,13)/t5-,6+,7+/m0/s1 Key: OLXZPDWKRNYJJZ-RRKCRQDMBK
Properties
Molecular formula	C₁₀H₁₃N₅O₃
Molar mass	251.24192
N (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Deoxyadenosine is a deoxyribonucleoside. It is a derivative of the nucleoside adenosine, differing from the latter by the replacement of a hydroxyl group (-OH) by hydrogen (-H) at the 2' position of its ribose sugar moiety. Deoxyadenosine is the DNA nucleoside A, which pairs with deoxythymidine (T) in double-stranded DNA.

References

Nucleic acid constituents

Ribonucleoside	Adenosine · Guanosine · 5-Methyluridine · Uridine · Cytidine

Deoxyribonucleoside	Deoxyadenosine · Deoxyguanosine · Thymidine · Deoxyuridine · Deoxycytidine

Nucleotide
(Nucleoside monophosphate)

Nucleoside diphosphate

biochemical families: prot · nucl · carb (glpr, alco, glys) · lipd (fata/i, phld, strd, gllp, eico) · amac/i · ncbs/i · ttpy/i