XenoSite

Azocarmine g free acid

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Azocarmine g free acid Epoxidation prediction
O=S(=O)(O)c1ccc(N=c2cc3n(-c4ccccc4)c4ccccc4nc-3c3c2C2OC2(S(=O)(=O)O)C=C3)cc1 N-Dealkylation prediction
O=S(=O)(O)c1ccc(N=C2C=C(Nc3ccccc3)C(=Nc3ccccc3O)C3=C2C2OC2(S(=O)(=O)O)C=C3)cc1 stable oxygenation prediction
O=S(=O)(O)c1ccc(N=C2C=C(Nc3ccccc3)C(=Nc3ccccc3O)C3=C2C2OC2(S(=O)(=O)O)C=C3)cc1 unstable oxygenation prediction
O=S(=O)(O)c1ccc(N=C2C=C(Nc3ccccc3)C(=Nc3ccccc3O)C3=C2C2OC2(S(=O)(=O)O)C=C3)cc1 dehydrogenation prediction
O=S(=O)(O)c1ccc(N=C2C=C(Nc3ccccc3)C(=Nc3ccccc3O)C3=C2C2OC2(S(=O)(=O)O)C=C3)cc1 reduction prediction
O=S(=O)(O)c1ccc(N=C2C=C(Nc3ccccc3)C(=Nc3ccccc3O)C3=C2C2OC2(S(=O)(=O)O)C=C3)cc1 hydrolysis prediction
O=S(=O)(O)c1ccc(N=C2C=C(Nc3ccccc3)C(=Nc3ccccc3O)C3=C2C(O)C(S(=O)(=O)O)C=C3)cc1 Quinonation prediction
quinone formation · 0.00
O=C1C=CC(=NC2=CC(=Nc3ccc(S(=O)(=O)O)cc3)C3=C(C=CC(S(=O)(=O)O)C3O)C2=Nc2ccccc2O)C=C1
Probability scale from 0.0 to 1.0