XenoSite

Anthraniloyl-coa

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Anthraniloyl-coa Quinonation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(n2cnc3c(N)ncnc32)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC(=O)C(=O)C=C1N Epoxidation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=NC34OC3(N)N=CN=C24)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC(=O)C(=O)C=C1N stable oxygenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=NC34OC3(N)N=CN=C24)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC(=O)C(=O)C=C1N unstable oxygenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=NC34OC3(N)N=CN=C24)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC(=O)C(=O)C=C1N dehydrogenation prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=NC34OC3(N)N=CN=C24)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC(=O)C(=O)C=C1N reduction prediction
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=NC34OC3(N)N=CN=C24)C(O)C1OP(=O)([O-])[O-])C(O)C(=O)NCCC(=O)NCCSC(=O)C1=CC(=O)C(=O)C=C1N hydrolysis prediction

Select a metabolite to form the next generation.

Showing 5 of 224 metabolites

Probability scale from 0.0 to 1.0