XenoSite

Aporphine

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Aporphine Epoxidation prediction
CN1CCc2cccc3c2C1CC1=CC2OC2C=C13 Quinonation prediction
CN1CCC2=CC(=O)C=C3C4=CC5OC5C=C4CC1=C23 N-Dealkylation prediction
CNC1=C2C(CC(=O)O)=CC(=O)C=C2C2=CC3OC3C=C2C1 stable oxygenation prediction
CNC1=C2C(CC(=O)O)=CC(=O)C=C2C2=CC3OC3C=C2C1 unstable oxygenation prediction
CNC1=C2C(CC(=O)O)=CC(=O)C=C2C2=CC3OC3C=C2C1 dehydrogenation prediction
CNC1=C2C(CC(=O)O)=CC(=O)C=C2C2=CC3OC3C=C2C1 reduction prediction
CNC1=C2C(CC(=O)O)=CC(=O)C=C2C2=CC3OC3C=C2C1 hydrolysis prediction

Methanol

CHEBI
dealkylation · 0.44
Methanol
Probability scale from 0.0 to 1.0