Chemistry:Deoxyguanosine monophosphate

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Deoxyguanosine monophosphate
Skeletal formula of deoxyguanosine monophosphate
Space-filling model of the deoxyguanosine monophosphate anion
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
UNII
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).
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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

References