Deoxyguanosine monophosphate
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| Names | |
|---|---|
| IUPAC name 2′-Deoxyguanylic acid | |
| Systematic IUPAC name [(2R,3S,5R)-5-(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl dihydrogen phosphate | |
| Identifiers | |
3D model (JSmol) | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.011.808 |
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
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| Properties | |
| C10H14N5O7P | |
| Molar mass | 347.2243 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Deoxyguanosine monophosphate (dGMP), also known as deoxyguanylic acid or deoxyguanylate in its conjugate acid and conjugate base forms, respectively, is a derivative of the common nucleotide guanosine triphosphate (GTP), in which the –OH (hydroxyl) group on the 2' carbon on the ribose has been reduced to just a hydrogen atom (hence the "deoxy-" part of the name). It is used as a monomer in DNA.[1]
See also
References
- ^ Müller, Sabine (2008-09-08). Nucleic Acids from A to Z. John Wiley & Sons. ISBN 9783527622535.

