XenoSite

Anthraniloyl-coa

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Anthraniloyl-coa N-Dealkylation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(=O)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)c1ccccc1N Epoxidation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(=O)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC2OC2C=C1N stable oxygenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(=O)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC2OC2C=C1N unstable oxygenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(=O)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC2OC2C=C1N dehydrogenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(=O)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC2OC2C=C1N reduction prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(=O)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC2OC2C=C1N hydrolysis prediction

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