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(-c2ccnc3c2ccc2c(-c4ccc(S(=O)(=O)O)cc4)cc[n+]([O-])c23)cc1 Quinonation prediction
O=C1C(=O)C2=C(c3ccc(S(=O)(=O)O)cc3)C=C[N+](=O)C2=C2[N-]C=CC(c3ccc(S(=O)(=O)O)cc3)=C12 N-Dealkylation prediction
NC1=C2C(=C(c3ccc(S(=O)(=O)O)cc3)C=C[N+]2=O)C(=O)C(=O)C1=C(C=CO)c1ccc(S(=O)(=O)O)cc1 Epoxidation prediction
NC1=C2C(=C(c3ccc(S(=O)(=O)O)cc3)C=C[N+]2=O)C(=O)C(=O)C1=C(c1ccc(S(=O)(=O)O)cc1)C1OC1O stable oxygenation prediction
NC1=C2C(=C(c3ccc(S(=O)(=O)O)cc3)C=C[N+]2=O)C(=O)C(=O)C1=C(c1ccc(S(=O)(=O)O)cc1)C1OC1O unstable oxygenation prediction
NC1=C2C(=C(c3ccc(S(=O)(=O)O)cc3)C=C[N+]2=O)C(=O)C(=O)C1=C(c1ccc(S(=O)(=O)O)cc1)C1OC1O dehydrogenation prediction
NC1=C2C(=C(c3ccc(S(=O)(=O)O)cc3)C=C[N+]2=O)C(=O)C(=O)C1=C(c1ccc(S(=O)(=O)O)cc1)C1OC1O reduction prediction
NC1=C2C(=C(c3ccc(S(=O)(=O)O)cc3)C=C[N+]2=O)C(=O)C(=O)C1=C(c1ccc(S(=O)(=O)O)cc1)C1OC1O hydrolysis prediction

Maximum generation reached — metabolites here can't start another hop.

Showing 5 of 158 metabolites

Probability scale from 0.0 to 1.0