Chemical Component Summary

NameAMINOPHOSPHONIC ACID-GUANYLATE ESTER
Identifiers[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxyphosphonamidic acid
FormulaC10 H16 N6 O10 P2
Molecular Weight442.216
TypeNON-POLYMER
Isomeric SMILESc1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(N)O)O)O)N=C(NC2=O)N
InChIInChI=1S/C10H16N6O10P2/c11-10-14-7-4(8(19)15-10)13-2-16(7)9-6(18)5(17)3(25-9)1-24-28(22,23)26-27(12,20)21/h2-3,5-6,9,17-18H,1H2,(H,22,23)(H3,12,20,21)(H3,11,14,15,19)/t3-,5-,6-,9-/m1/s1
InChIKeyZGPDMUBRWRJAQQ-UUOKFMHZSA-N

Chemical Details

Formal Charge0
Atom Count44
Chiral Atom Count6
Bond Count46
Aromatic Bond Count10

Drug Info: DrugBank

DrugBank IDDB02623 
NameAminophosphonic acid-guanylate ester
Groups experimental
SynonymsAminophosphonic acid-guanylate ester

Drug Targets

NameTarget SequencePharmacological ActionActions
Cell division control protein 42 homologMQTIKCVVVGDGAVGKTCLLISYTTNKFPSEYVPTVFDNYAVTVMIGGEP...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 444148, 135612789, 6602185, 135480785, 5288454