XenoSite

Aclacinomycin s

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Aclacinomycin s Epoxidation prediction
CCC1(O)CC(OC2CC([NH+](C)C)C(OC3CC(O)C(O)C(C)O3)C(C)O2)[c-]2c(cc3c(c2=O)C(=O)C2=C(C=CC4OC24O)C3=O)C1C(=O)OC stable oxygenation prediction
CCC1(O)CC(OC2CC([NH+](C)C)C(OC3CC(O)C(O)C(C)O3)C(C)O2)[c-]2c(cc3c(c2=O)C(=O)C2=C(C=CC4OC24O)C3=O)C1C(=O)OC unstable oxygenation prediction
CCC1(O)CC(OC2CC([NH+](C)C)C(OC3CC(O)C(O)C(C)O3)C(C)O2)[c-]2c(cc3c(c2=O)C(=O)C2=C(C=CC4OC24O)C3=O)C1C(=O)OC dehydrogenation prediction
CCC1(O)CC(OC2CC([NH+](C)C)C(OC3CC(O)C(O)C(C)O3)C(C)O2)[c-]2c(cc3c(c2=O)C(=O)C2=C(C=CC4OC24O)C3=O)C1C(=O)OC reduction prediction
CCC1(O)CC(OC2CC([NH+](C)C)C(OC3CC(O)C(O)C(C)O3)C(C)O2)[c-]2c(cc3c(c2=O)C(=O)C2=C(C=CC4OC24O)C3=O)C1C(=O)OC hydrolysis prediction
CCC1(O)CC(OC2CC([NH+](C)C)C(OC3CC(O)C(O)C(C)O3)C(C)O2)c2c(cc3c(c2[O-])C(=O)C2=C(C=CC4OC24O)C3O)C1C(=O)OC Quinonation prediction
CCC1(O)CC(OC2CC([NH+](C)C)C(OC3CC(O)C(O)C(C)O3)C(C)O2)=C2C(=O)c3c([O-])c4c(c(O)c3C=C2C1C(=O)OC)C=CC1OC41O UGT Conjugation prediction
glucuronidation · 0.30
*Oc1c2c(c([O-])c3c1C=CC1OC31O)C(=O)C1=C(OC3CC([NH+](C)C)C(OC4CC(O)C(O)C(C)O4)C(C)O3)CC(O)(CC)C(C(=O)OC)C1=C2 |$GlcA;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;$|
Probability scale from 0.0 to 1.0