Deoxyguanosine monophosphate
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 | |
CAS Number |
|
3D model (JSmol) |
|
ChEBI |
|
ChemSpider |
|
ECHA InfoCard | 100.011.808 |
IUPHAR/BPS |
|
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | 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). N verify (what is YN ?) Infobox references |
Chemical compound
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 nucleic acid guanosine triphosphate (GTP), in which the –OH (hydroxyl) group on the 2' carbon on the nucleotide's pentose 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
- Cofactor
- Guanosine
- Nucleic acid
References
- ^ Müller, Sabine (2008-09-08). Nucleic Acids from A to Z. John Wiley & Sons. ISBN 9783527622535.
- 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