XenoSite

Anileridine

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Anileridine Quinonation prediction
CCOC(=O)C1(c2ccccc2)CCN(CCC2=CC(=O)C(=N)C=C2)CC1 Epoxidation prediction
CCOC(=O)C1(c2ccccc2)CCN(CCC23C=CC(=N)C(=O)C2O3)CC1 stable oxygenation prediction
CCOC(=O)C1(c2ccccc2)CCN(CCC23C=CC(=N)C(=O)C2O3)CC1 unstable oxygenation prediction
CCOC(=O)C1(c2ccccc2)CCN(CCC23C=CC(=N)C(=O)C2O3)CC1 dehydrogenation prediction
CCOC(=O)C1(c2ccccc2)CCN(CCC23C=CC(=N)C(=O)C2O3)CC1 reduction prediction
CCOC(=O)C1(c2ccccc2)CCN(CCC23C=CC(=N)C(=O)C2O3)CC1 hydrolysis prediction
N=C1C=CC2(CCN3CCC(C=O)(c4ccccc4)CC3)OC2C1=O gsh prediction
N=C1C=CC2(CCN3CCC(C=O)(c4ccccc4)CC3)OC2C1=O protein prediction
N=C1C=CC2(CCN3CCC(C=O)(c4ccccc4)CC3)OC2C1=O cyanide prediction
N=C1C=CC2(CCN3CCC(C=O)(c4ccccc4)CC3)OC2C1=O dna prediction

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Showing 5 of 16 metabolites

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