XenoSite

Acemetacin

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Acemetacin Epoxidation prediction
COC12C=c3c(CC(=O)OCC(=O)O)c(C)n(C(=O)c4ccc(Cl)cc4)c3=CC1O2 Quinonation prediction
C=c1c(=CC(=O)OCC(=O)O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 stable oxygenation prediction
C=c1c(=CC(=O)OCC(=O)O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 unstable oxygenation prediction
C=c1c(=CC(=O)OCC(=O)O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 dehydrogenation prediction
C=c1c(=CC(=O)OCC(=O)O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 reduction prediction
C=c1c(=CC(=O)OCC(=O)O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 hydrolysis prediction
C=c1c(=CC=O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 stable oxygenation prediction
C=c1c(=CC=O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 unstable oxygenation prediction
C=c1c(=CC=O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 dehydrogenation prediction
C=c1c(=CC=O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 reduction prediction
C=c1c(=CC=O)c2c(n1C(=O)c1ccc(Cl)cc1)=CC1OC1(OC)C=2 hydrolysis prediction

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