XenoSite

Azocarmine g anion

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Azocarmine g anion Epoxidation prediction
O=S(=O)([O-])c1ccc(Nc2cc3c(nc4c([n+]3-c3ccccc3)C=CC3OC43)c3ccc(S(=O)(=O)[O-])cc23)cc1 Quinonation prediction
O=S(=O)([O-])c1ccc(N=C2C=c3c(nc4c([n+]3-c3ccccc3)C=CC3OC=43)-c3ccc(S(=O)(=O)[O-])cc32)cc1 stable oxygenation prediction
O=S(=O)([O-])c1ccc(N=C2C=c3c(nc4c([n+]3-c3ccccc3)C=CC3OC=43)-c3ccc(S(=O)(=O)[O-])cc32)cc1 unstable oxygenation prediction
O=S(=O)([O-])c1ccc(N=C2C=c3c(nc4c([n+]3-c3ccccc3)C=CC3OC=43)-c3ccc(S(=O)(=O)[O-])cc32)cc1 dehydrogenation prediction
O=S(=O)([O-])c1ccc(N=C2C=c3c(nc4c([n+]3-c3ccccc3)C=CC3OC=43)-c3ccc(S(=O)(=O)[O-])cc32)cc1 reduction prediction
O=S(=O)([O-])c1ccc(N=C2C=c3c(nc4c([n+]3-c3ccccc3)C=CC3OC=43)-c3ccc(S(=O)(=O)[O-])cc32)cc1 hydrolysis prediction
hydrogenation · 0.19
O=S(=O)([O-])c1ccc2c(c1)C(=Nc1ccc([SH](=O)([O-])O)cc1)C=c1c-2nc2c([n+]1-c1ccccc1)C=CC1OC=21
Probability scale from 0.0 to 1.0