XenoSite

Aristolochic acid a

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Aristolochic acid a Quinonation prediction
COc1cccc2c3c(c([N+](=O)[O-])cc12)C(C(=O)O)=CC(=O)C3=O Epoxidation prediction
COC1=CC2OC2c2c1cc([N+](=O)[O-])c1c2C(=O)C(=O)C=C1C(=O)O stable oxygenation prediction
COC1=CC2OC2c2c1cc([N+](=O)[O-])c1c2C(=O)C(=O)C=C1C(=O)O unstable oxygenation prediction
COC1=CC2OC2c2c1cc([N+](=O)[O-])c1c2C(=O)C(=O)C=C1C(=O)O dehydrogenation prediction
COC1=CC2OC2c2c1cc([N+](=O)[O-])c1c2C(=O)C(=O)C=C1C(=O)O reduction prediction
COC1=CC2OC2c2c1cc([N+](=O)[O-])c1c2C(=O)C(=O)C=C1C(=O)O hydrolysis prediction

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Showing 5 of 115 metabolites

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