Deoxyadenosine monophosphate

Deoxyadenosine monophosphate

Identifiers
CAS Registry Number	653-63-4 Y
ChEBI	CHEBI:17713 Y
ChemSpider	12079 Y
InChI InChI=1S/C10H14N5O6P/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(21-7)2-20-22(17,18)19/h3-7,16H,1-2H2,(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1 Y Key: KHWCHTKSEGGWEX-RRKCRQDMSA-N Y InChI=1/C10H14N5O6P/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(21-7)2-20-22(17,18)19/h3-7,16H,1-2H2,(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1 Key: KHWCHTKSEGGWEX-RRKCRQDMBS
Jmol-3D images	Image
MeSH	Deoxyadenosine+monophosphate
PubChem	621
SMILES c1nc(c2c(n1)n(cn2)[C@H]3C[C@@H]([C@H](O3)COP(=O)(O)O)O)N
Properties
Chemical formula	C10H14N5O6P
Molar mass	331.222 g/mol
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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Infobox references

Deoxyadenosine monophosphate, also known as deoxyadenylate, or dAMP, is a derivative of the common nucleic acid AMP, or adenosine monophosphate, 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). Deoxyadenosine monophosphate is abbreviated dAMP. It is a monomer used in DNA.

See also

• Nucleic acid
• DNA metabolism
• Cofactor
• Guanosine
• Cyclic AMP (cAMP)
• ATP

Sources

• Deoxyadenosine monophosphate at HMDB