G2P

PHOSPHOMETHYLPHOSPHONIC ACID GUANYLATE ESTER



Chemical Component Summary

NamePHOSPHOMETHYLPHOSPHONIC 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]methyl-phosphonooxy-phosphinic acid
FormulaC11 H18 N5 O13 P3
Molecular Weight521.208
TypeNON-POLYMER
Isomeric SMILESc1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(C[P@@](=O)(O)OP(=O)(O)O)O)O)O)N=C(NC2=O)N
InChIInChI=1S/C11H18N5O13P3/c12-11-14-8-5(9(19)15-11)13-2-16(8)10-7(18)6(17)4(28-10)1-27-30(20,21)3-31(22,23)29-32(24,25)26/h2,4,6-7,10,17-18H,1,3H2,(H,20,21)(H,22,23)(H2,24,25,26)(H3,12,14,15,19)/t4-,6-,7-,10-/m1/s1
InChIKeyGXTIEXDFEKYVGY-KQYNXXCUSA-N

Chemical Details

Formal Charge0
Atom Count50
Chiral Atom Count6
Bond Count52
Aromatic Bond Count10

Drug Info: DrugBank

DrugBank IDDB03532 
NamePhosphomethylphosphonic acid guanylate ester
Groups experimental
SynonymsPhosphomethylphosphonic acid guanylate ester

Drug Targets

NameTarget SequencePharmacological ActionActions
Cell division protein FtsZMGFDLDVEKKKENRNIPQANNLKIKVIGVGGAGNNAINRMIEIGIHGVEF...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 5288325, 449108, 135440070