Chemical Component Summary

NameADENOSINE-5'-DIPHOSPHATE-GLUCOSE
SynonymsADENOSINE-5'-MONOPHOSPHATE GLUCOPYRANOSYL-MONOPHOSPHATE ESTER
Identifiers[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl] [(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] hydrogen phosphate
FormulaC16 H25 N5 O15 P2
Molecular Weight589.342
TypeNON-POLYMER
Isomeric SMILESc1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@@](=O)(O)O[C@@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O)N
InChIInChI=1S/C16H25N5O15P2/c17-13-7-14(19-3-18-13)21(4-20-7)15-11(26)9(24)6(33-15)2-32-37(28,29)36-38(30,31)35-16-12(27)10(25)8(23)5(1-22)34-16/h3-6,8-12,15-16,22-27H,1-2H2,(H,28,29)(H,30,31)(H2,17,18,19)/t5-,6-,8-,9-,10+,11-,12-,15-,16-/m1/s1
InChIKeyWFPZSXYXPSUOPY-ROYWQJLOSA-N

Chemical Details

Formal Charge0
Atom Count63
Chiral Atom Count11
Bond Count66
Aromatic Bond Count10

Drug Info: DrugBank

DrugBank IDDB01774 
NameAdenosine-5'-Monophosphate Glucopyranosyl-Monophosphate Ester
Groups experimental
DescriptionServes as the glycosyl donor for formation of bacterial glycogen, amylose in green algae, and amylopectin in higher plants. [PubChem]
SynonymsAdenosine-5'-Monophosphate Glucopyranosyl-Monophosphate Ester

Drug Targets

NameTarget SequencePharmacological ActionActions
ADP-L-glycero-D-manno-heptose-6-epimeraseMIIVTGGAGFIGSNIVKALNDKGITDILVVDNLKDGTKFVNLVDLNIADY...unknown
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682

Related Resource References

Resource NameReference
PubChem 16500
ChEMBL CHEMBL227552
ChEBI CHEBI:15751