Deoxyinosine monophosphate

Deoxyinosine monophosphate
Names
	IUPAC name 2’-Deoxy-5’-inosinic acid
Identifiers
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:28806;
ChemSpider	82650;
ECHA InfoCard	100.020.216
PubChem CID	91531;
CompTox Dashboard (EPA)	DTXSID60937065 ;
	InChI InChI=1S/C10H13N4O7P/c15-5-1-7(21-6(5)2-20-22(17,18)19)14-4-13-8-9(14)11-3-12-10(8)16/h3-7,15H,1-2H2,(H,11,12,16)(H2,17,18,19)/t5-,6+,7+/m0/s1 Key: PHNGFPPXDJJADG-RRKCRQDMSA-N; InChI=1/C10H13N4O7P/c15-5-1-7(21-6(5)2-20-22(17,18)19)14-4-13-8-9(14)11-3-12-10(8)16/h3-7,15H,1-2H2,(H,11,12,16)(H2,17,18,19)/t5-,6+,7+/m0/s1 Key: PHNGFPPXDJJADG-RRKCRQDMBF;
	SMILES O=C3/N=C\Nc1c3ncn1[C@@H]2O[C@@H]([C@@H](O)C2)COP(=O)(O)O;
Properties
Chemical formula	C10H13N4O7P
Molar mass	332.209 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Deoxyinosine monophosphate (dIMP) is a nucleotide monophosphate and a derivative of inosinic acid. It can be formed by the deamination of the purine base in deoxyadenosine monophosphate (dAMP). The enzyme deoxyribonucleoside triphosphate pyrophosphohydrolase, encoded by YJR069C in S. cerevisiae and containing (d)ITPase and (d)XTPase activities, hydrolyses dITP releasing pyrophosphate and dIMP.^[1]

References

^ Davies O, Mendes P, Smallbone K, Malys N (2012). "Characterisation of multiple substrate-specific (d)ITP/(d)XTPase and modelling of deaminated purine nucleotide metabolism". BMB Reports. 45 (4): 259–64. doi:10.5483/BMBRep.2012.45.4.259. PMID 22531138.