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 stable oxygenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(n2cnc3c(N)ncnc32)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O unstable oxygenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(n2cnc3c(N)ncnc32)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O dehydrogenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(n2cnc3c(N)ncnc32)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O reduction prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(n2cnc3c(N)ncnc32)C(O)C1OP(=O)([O-])[O-])C(O)C(N)=O hydrolysis prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(n2cnc3c(N)ncnc32)C(O)C1O)C(O)C(N)=O Epoxidation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(n2cnc3c2N=CN2OC32N)C(O)C1O)C(O)C(N)=O UGT Conjugation prediction
glucuronidation · 0.07
*OC1C(O)C(COP(=O)([O-])OP(=O)([O-])OCC(C)(C)C(O)C(N)=O)OC1n1cnc2c1N=CN1OC21N |$GlcA;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;$|
Probability scale from 0.0 to 1.0