XenoSite

Bathophenanthroline disulfonic acid

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Bathophenanthroline disulfonic acid stable oxygenation prediction
Bathophenanthroline disulfonic acid unstable oxygenation prediction
Bathophenanthroline disulfonic acid dehydrogenation prediction
Bathophenanthroline disulfonic acid reduction prediction
Bathophenanthroline disulfonic acid hydrolysis prediction
O=S(=O)(O)c1ccc(C2=C3C=Cc4c(-c5ccc(S(=O)(=O)O)cc5)ccnc4C34ON4C=C2)cc1 N-Dealkylation prediction
O=C=CC(=C1C=Cc2c(-c3ccc(S(=O)(=O)O)cc3)ccnc2C12NO2)c1ccc(S(=O)(=O)O)cc1 Quinonation prediction
O=C=CC(=C1C=CC2=C(N=CC(=O)C2=C2C=CC(S(=O)(=O)O)=CC2=O)C12NO2)c1ccc(S(=O)(=O)O)cc1 stable oxygenation prediction
O=C=CC(=C1C=CC2=C(N=CC(=O)C2=C2C=CC(S(=O)(=O)O)=CC2=O)C12NO2)c1ccc(S(=O)(=O)O)cc1 unstable oxygenation prediction
O=C=CC(=C1C=CC2=C(N=CC(=O)C2=C2C=CC(S(=O)(=O)O)=CC2=O)C12NO2)c1ccc(S(=O)(=O)O)cc1 dehydrogenation prediction
O=C=CC(=C1C=CC2=C(N=CC(=O)C2=C2C=CC(S(=O)(=O)O)=CC2=O)C12NO2)c1ccc(S(=O)(=O)O)cc1 reduction prediction
O=C=CC(=C1C=CC2=C(N=CC(=O)C2=C2C=CC(S(=O)(=O)O)=CC2=O)C12NO2)c1ccc(S(=O)(=O)O)cc1 hydrolysis prediction

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