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 N-Dealkylation prediction
N=C1C(C2(c3ccc(S(=O)(=O)O)cc3)OC2C(=O)O)=CC=C2C(c3ccc(S(=O)(=O)O)cc3)=CC(=O)N=C12 stable oxygenation prediction
N=C1C(C2(c3ccc(S(=O)(=O)O)cc3)OC2C(=O)O)=CC=C2C(c3ccc(S(=O)(=O)O)cc3)=CC(=O)N=C12 unstable oxygenation prediction
N=C1C(C2(c3ccc(S(=O)(=O)O)cc3)OC2C(=O)O)=CC=C2C(c3ccc(S(=O)(=O)O)cc3)=CC(=O)N=C12 dehydrogenation prediction
N=C1C(C2(c3ccc(S(=O)(=O)O)cc3)OC2C(=O)O)=CC=C2C(c3ccc(S(=O)(=O)O)cc3)=CC(=O)N=C12 reduction prediction
N=C1C(C2(c3ccc(S(=O)(=O)O)cc3)OC2C(=O)O)=CC=C2C(c3ccc(S(=O)(=O)O)cc3)=CC(=O)N=C12 hydrolysis prediction
hydrogenation · 0.07
N=C1C2=NC(=O)C=C(c3ccc(S(=O)(=O)O)cc3)C2=CCC1C1(c2ccc(S(=O)(=O)O)cc2)OC1C(=O)O
Probability scale from 0.0 to 1.0