Substrate
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Generation 1
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Generation 2
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Generation 3
XenoSite
Anileridine
CCOC(=O)C1(c2ccccc2)CCN(CCc2ccc(N)cc2)CC1
CHEBI
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Description
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Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
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Generation 1
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CCOC(=O)C1(C2=CC3OC3C=C2)CCN(CCc2ccc(N)cc2)CC1
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Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
About this model
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stable oxygenation
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unstable oxygenation
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dehydrogenation
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reduction
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hydrolysis
Generation 2
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Nc1ccc(CC(=O)O)cc1
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Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
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Generation 3
Show metabolites
(<em>p</em>-hydroxyphenyl)acetic acid
O=C(O)Cc1ccc(O)cc1
CHEBI
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Description
▾
Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
About this model
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stable oxygenation
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unstable oxygenation
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dehydrogenation
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reduction
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hydrolysis
Generation 4
Select a metabolite to form the next generation.
hydroxylation
Probability 0.07
0.07
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4-hydroxy-<small>d</small>-mandelic acid
hydrogenation
Probability 0.06
0.06
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hydroxylation
Probability 0.05
0.05
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Homoprotocatechuic acid
dehydrogenation
Probability 0.04
0.04
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dealkylation
Probability 0.03
0.03
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Paracresol
Showing 5 of 41 metabolites
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