XenoSite

Bathophenanthroline disulfonic acid

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Bathophenanthroline disulfonic acid Quinonation prediction
O=C1C=C(c2ccc(S(=O)(=O)O)cc2)c2ccc3c(c2=N1)=NC(=O)C=C3c1ccc(S(=O)(=O)O)cc1 Epoxidation prediction
O=C1C=C(c2ccc(S(=O)(=O)O)cc2)c2ccc3c(c2=N1)=NC(=O)C1OC31c1ccc(S(=O)(=O)O)cc1 stable oxygenation prediction
O=C1C=C(c2ccc(S(=O)(=O)O)cc2)c2ccc3c(c2=N1)=NC(=O)C1OC31c1ccc(S(=O)(=O)O)cc1 unstable oxygenation prediction
O=C1C=C(c2ccc(S(=O)(=O)O)cc2)c2ccc3c(c2=N1)=NC(=O)C1OC31c1ccc(S(=O)(=O)O)cc1 dehydrogenation prediction
O=C1C=C(c2ccc(S(=O)(=O)O)cc2)c2ccc3c(c2=N1)=NC(=O)C1OC31c1ccc(S(=O)(=O)O)cc1 reduction prediction
O=C1C=C(c2ccc(S(=O)(=O)O)cc2)c2ccc3c(c2=N1)=NC(=O)C1OC31c1ccc(S(=O)(=O)O)cc1 hydrolysis prediction
O=C1N=c2c(ccc3c2=NC(O)C=C3c2ccc(S(=O)(=O)O)cc2)C2(c3ccc(S(=O)(=O)O)cc3)OC12 N-Dealkylation prediction
dealkylation · 0.68
N=C1C(C(=CC(O)O)c2ccc(S(=O)(=O)O)cc2)=CC=C2C1=NC(=O)C1OC21c1ccc(S(=O)(=O)O)cc1
Probability scale from 0.0 to 1.0