XenoSite

Actinorhodin

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Actinorhodin Quinonation prediction
CC1=c2c(O)c3c(c(O)c2=CC(CC(=O)[O-])O1)C(=O)C=C(C1=CC(=O)c2c(O)c4c(c([O-])c2C1=O)C(C)OC(CC(=O)[O-])C4)C3=O stable oxygenation prediction
CC1=c2c(O)c3c(c(O)c2=CC(CC(=O)[O-])O1)C(=O)C=C(C1=CC(=O)c2c(O)c4c(c([O-])c2C1=O)C(C)OC(CC(=O)[O-])C4)C3=O unstable oxygenation prediction
CC1=c2c(O)c3c(c(O)c2=CC(CC(=O)[O-])O1)C(=O)C=C(C1=CC(=O)c2c(O)c4c(c([O-])c2C1=O)C(C)OC(CC(=O)[O-])C4)C3=O dehydrogenation prediction
CC1=c2c(O)c3c(c(O)c2=CC(CC(=O)[O-])O1)C(=O)C=C(C1=CC(=O)c2c(O)c4c(c([O-])c2C1=O)C(C)OC(CC(=O)[O-])C4)C3=O reduction prediction
CC1=c2c(O)c3c(c(O)c2=CC(CC(=O)[O-])O1)C(=O)C=C(C1=CC(=O)c2c(O)c4c(c([O-])c2C1=O)C(C)OC(CC(=O)[O-])C4)C3=O hydrolysis prediction
CC1=c2c(O)c3c(c(O)c2=CC(CC(=O)[O-])O1)CC=C(C1=CC(=O)c2c(O)c4c(c([O-])c2C1=O)C(C)OC(CC(=O)[O-])C4)C3=O Epoxidation prediction
CC1=c2c(O)c3c(c(O)c2=CC(CC(=O)[O-])O1)CC1OC1(C1=CC(=O)C2=C(O)C4=C(C(=O)C2=C1[O-])C(C)OC(CC(=O)[O-])C4)C3=O UGT Conjugation prediction

Select a metabolite to form the next generation.

Probability scale from 0.0 to 1.0