Deoxyguanosine
Names | |
---|---|
IUPAC name 2-Amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChEBI |
|
ChEMBL |
|
ChemSpider |
|
ECHA InfoCard | 100.012.278 |
MeSH | Deoxyguanosine |
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
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). N verify (what is YN ?) Infobox references |
Chemical compound
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]
See also
References
- v
- t
- e
Nucleic acid constituents
- Purine
- Pyrimidine
- Unnatural base pair (UBP)
Ribonucleoside |
|
---|---|
Deoxyribonucleoside |
|
(Nucleoside monophosphate)
Ribonucleotide | |
---|---|
Deoxyribonucleotide | |
Cyclic nucleotide |
This biochemistry article is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e