XenoSite

Chlortetracycline

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Chlortetracycline N-Dealkylation prediction
CNC1C(O)=C(C(N)=O)C(=O)C2(O)C(O)=C3C(=O)c4c(O)ccc(Cl)c4C(C)(O)C3CC12 Epoxidation prediction
CNC1C(O)=C(C(N)=O)C(=O)C2(O)C1CC1C(C)(O)c3c(Cl)ccc(O)c3C(=O)C13OC23O Quinonation prediction
CNC1C(O)=C(C(N)=O)C(=O)C2(O)C1CC1C(C)(O)C3=C(Cl)C(=O)C(=O)C(O)=C3C(=O)C13OC23O stable oxygenation prediction
CNC1C(O)=C(C(N)=O)C(=O)C2(O)C1CC1C(C)(O)C3=C(Cl)C(=O)C(=O)C(O)=C3C(=O)C13OC23O unstable oxygenation prediction
CNC1C(O)=C(C(N)=O)C(=O)C2(O)C1CC1C(C)(O)C3=C(Cl)C(=O)C(=O)C(O)=C3C(=O)C13OC23O dehydrogenation prediction
CNC1C(O)=C(C(N)=O)C(=O)C2(O)C1CC1C(C)(O)C3=C(Cl)C(=O)C(=O)C(O)=C3C(=O)C13OC23O reduction prediction
CNC1C(O)=C(C(N)=O)C(=O)C2(O)C1CC1C(C)(O)C3=C(Cl)C(=O)C(=O)C(O)=C3C(=O)C13OC23O hydrolysis prediction
dealkylation · 0.35
CC1(O)C2=C(Cl)C(=O)C(=O)C(O)=C2C(=O)C23OC2(O)C2(O)C(=O)C(C(N)=O)=C(O)C(N)C2CC13
Probability scale from 0.0 to 1.0