Deoxyadenosine triphosphate

Deoxyadenosine triphosphate
Names
	IUPAC name [[(2R,3S,5R)-5-(6-aminopurin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
	Other names dATP, 2'-deoxyadenosine triphosphate
Identifiers
CAS Number	1927-31-7 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:16284 ;
ChEMBL	ChEMBL335538 ;
ChemSpider	15194 = = = ;
ECHA InfoCard	100.016.058
IUPHAR/BPS	1760;
PubChem CID	15993;
CompTox Dashboard (EPA)	DTXSID10895848 ;
	InChI InChI=1S/C10H16N5O12P3/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(25-7)2-24-29(20,21)27-30(22,23)26-28(17,18)19/h3-7,16H,1-2H2,(H,20,21)(H,22,23)(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1 = Key: SUYVUBYJARFZHO-RRKCRQDMSA-N = ; InChI=1/C10H16N5O12P3/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(25-7)2-24-29(20,21)27-30(22,23)26-28(17,18)19/h3-7,16H,1-2H2,(H,20,21)(H,22,23)(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1 Key: SUYVUBYJARFZHO-RRKCRQDMBD;
	SMILES O=P(O)(O)OP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n2cnc1c(ncnc12)N)C[C@@H]3O;
Properties
Chemical formula	C10H16N5O12P3
Molar mass	491.181623
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Deoxyadenosine triphosphate (dATP) is a nucleotide used in cells for DNA synthesis (or replication), as a substrate of DNA polymerase.

Deoxyadenosine triphosphate is produced from DNA by the action of nuclease P1, adenylate kinase, and pyruvate kinase.