Bathophenanthroline disulfonic acid

Phase 1 Reactivity Epoxidation Quinonation N-Dealkylation UGT Conjugation

Bathophenanthroline disulfonic acid N-Dealkylation prediction

Generation 1

Phase 1 Reactivity Epoxidation Quinonation N-Dealkylation UGT Conjugation

N=C1C(=C(C=CO)c2ccc(S(=O)(=O)O)cc2)C=Cc2c(-c3ccc(S(=O)(=O)O)cc3)ccnc21 Epoxidation prediction

Generation 2

Phase 1 Reactivity Epoxidation Quinonation N-Dealkylation UGT Conjugation

N=C1C(=C(C=CO)c2ccc(S(=O)(=O)O)cc2)C2OC2c2c(-c3ccc(S(=O)(=O)O)cc3)ccnc21 stable oxygenation prediction

N=C1C(=C(C=CO)c2ccc(S(=O)(=O)O)cc2)C2OC2c2c(-c3ccc(S(=O)(=O)O)cc3)ccnc21 unstable oxygenation prediction

N=C1C(=C(C=CO)c2ccc(S(=O)(=O)O)cc2)C2OC2c2c(-c3ccc(S(=O)(=O)O)cc3)ccnc21 dehydrogenation prediction

N=C1C(=C(C=CO)c2ccc(S(=O)(=O)O)cc2)C2OC2c2c(-c3ccc(S(=O)(=O)O)cc3)ccnc21 reduction prediction

N=C1C(=C(C=CO)c2ccc(S(=O)(=O)O)cc2)C2OC2c2c(-c3ccc(S(=O)(=O)O)cc3)ccnc21 hydrolysis prediction

Generation 3

Phase 1 Reactivity Epoxidation Quinonation N-Dealkylation UGT Conjugation

N=C1c2nccc(-c3ccc(S(=O)(=O)O)cc3)c2C2OC2C12OC2(C=CO)c1ccc(S(=O)(=O)O)cc1 Quinonation prediction

Generation 4

quinone formation · 0.00

Phase 1 Reactivity Epoxidation Quinonation N-Dealkylation UGT Conjugation

N=C1c2nccc(=C3C=CC(S(=O)(=O)O)=CC3=O)c2=C2OC2C12OC2(C=CO)c1ccc(S(=O)(=O)O)cc1