XenoSite

Anthraniloyl-coa

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Anthraniloyl-coa N-Dealkylation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(n2cnc3c(N)ncnc32)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O Quinonation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC([N+]2=c3ncnc(N)c3=NC2=O)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O stable oxygenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC([N+]2=c3ncnc(N)c3=NC2=O)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O unstable oxygenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC([N+]2=c3ncnc(N)c3=NC2=O)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O dehydrogenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC([N+]2=c3ncnc(N)c3=NC2=O)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O reduction prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC([N+]2=c3ncnc(N)c3=NC2=O)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O hydrolysis prediction
Nc1ncnc2c1=NC(=O)[N+]=2C1OC(CO[PH](=O)O)C(OP(=O)([O-])[O-])C1O UGT Conjugation prediction
glucuronidation · 0.27
*OC1C(OP(=O)([O-])[O-])C(CO[PH](=O)O)OC1[N+]1=c2ncnc(N)c2=NC1=O |$GlcA;;;;;;;;;;;;;;;;;;;;;;;;;;;$|
Probability scale from 0.0 to 1.0