Deoxyguanosine
Jump to navigation
Jump to search
This article needs additional citations for verification. (January 2016) |
Names | |
---|---|
IUPAC name
2-Amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one
| |
Identifiers | |
3D model (JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.012.278 |
MeSH | Deoxyguanosine |
PubChem CID
|
|
UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
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).
|
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
- ^ "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)".
Categories:
- Articles needing additional references from January 2016
- All articles needing additional references
- Articles without KEGG source
- Articles with changed EBI identifier
- ECHA InfoCard ID from Wikidata
- Articles containing unverified chemical infoboxes
- Chembox image size set
- Articles with short description
- Short description matches Wikidata
- Nucleosides
- Purines
- Hydroxymethyl compounds
- All stub articles
- Biochemistry stubs