Substrate
/
Generation 1
XenoSite
Acetylseneciphylline oxide
C=C1CC(=CC)C(=O)OC2CC[N+]3([O-])CC=C(COC(=O)C1(C)OC(C)=O)C23
CHEBI
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Description
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Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
About this model
stable oxygenation
unstable oxygenation
dehydrogenation
reduction
hydrolysis
Generation 1
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(15<i>e</i>)-12-hydroxy-13,19-didehydrosenecionan-11,16-dione 4 oxide
C=C1CC(=CC)C(=O)OC2CC[N+]3([O-])CC=C(COC(=O)C1(C)O)C23
CHEBI
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Description
▾
Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
About this model
stable oxygenation
unstable oxygenation
dehydrogenation
reduction
hydrolysis
Generation 2
Select a metabolite to form the next generation.
nitrogen reduction
Probability 0.56
0.56
[1,6]dioxacyclododecino[2,3,4-gh]pyrrolizine-2,7-dione, 3-ethylidene-3,4,5,6,9,11,13,14,14a,14b-decahydro-6-hydroxy-6-methyl-5-methylene-, (3z,6r,14ar,14br)-
nitrogen reduction
Probability 0.56
0.56
15o
hydrolysis
Probability 0.19
0.19
hydrolysis
Probability 0.19
0.19
hydrolysis
Probability 0.14
0.14
Showing 5 of 92 metabolites
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