Substrate
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Generation 1
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Generation 2
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Generation 3
XenoSite
Acemetacin
COc1ccc2c(c1)c(CC(=O)OCC(=O)O)c(C)n2C(=O)c1ccc(Cl)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
Show metabolites
COC12C=Cc3c(c(CC(=O)OCC(=O)O)c(C)n3C(=O)c3ccc(Cl)cc3)C1O2
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Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
About this model
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Generation 2
Show metabolites
4-chloranylbenzaldehyde
O=Cc1ccc(Cl)cc1
CHEBI
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Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
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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 3
Show metabolites
Parachlorophenol
Oc1ccc(Cl)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 0.10
0.10
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4-chlorocatechol
oxidative dehalogenation
Probability 0.10
0.10
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Acidum hydrochloricum
oxidative dehalogenation
Probability 0.10
0.10
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Hydroquinone
hydroxylation
Probability 0.08
0.08
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epoxidation
Probability 0.04
0.04
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Showing 5 of 32 metabolites
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