XenoSite

Abediterol

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Abediterol Epoxidation prediction
O=C1Nc2c(O)ccc(C(O)CNCCCCCCOCC(F)(F)c3ccccc3)c2C2OC12 Quinonation prediction
O=C1C=C(C(O)CNCCCCCCOCC(F)(F)c2ccccc2)C2=C(NC(=O)C3OC23)C1=O stable oxygenation prediction
O=C1C=C(C(O)CNCCCCCCOCC(F)(F)c2ccccc2)C2=C(NC(=O)C3OC23)C1=O unstable oxygenation prediction
O=C1C=C(C(O)CNCCCCCCOCC(F)(F)c2ccccc2)C2=C(NC(=O)C3OC23)C1=O dehydrogenation prediction
O=C1C=C(C(O)CNCCCCCCOCC(F)(F)c2ccccc2)C2=C(NC(=O)C3OC23)C1=O reduction prediction
O=C1C=C(C(O)CNCCCCCCOCC(F)(F)c2ccccc2)C2=C(NC(=O)C3OC23)C1=O hydrolysis prediction
O=C1C2=C(C(C(O)CNCCCCCCOCC(F)(F)c3ccccc3)=CC1O)C1OC1C(=O)N2 stable oxygenation prediction
O=C1C2=C(C(C(O)CNCCCCCCOCC(F)(F)c3ccccc3)=CC1O)C1OC1C(=O)N2 unstable oxygenation prediction
O=C1C2=C(C(C(O)CNCCCCCCOCC(F)(F)c3ccccc3)=CC1O)C1OC1C(=O)N2 dehydrogenation prediction
O=C1C2=C(C(C(O)CNCCCCCCOCC(F)(F)c3ccccc3)=CC1O)C1OC1C(=O)N2 reduction prediction
O=C1C2=C(C(C(O)CNCCCCCCOCC(F)(F)c3ccccc3)=CC1O)C1OC1C(=O)N2 hydrolysis prediction

Select a metabolite to form the next generation.

Showing 5 of 154 metabolites

Probability scale from 0.0 to 1.0