Substrate
/
Generation 1
/
Generation 2
XenoSite
Androstenediol
CC12CCC(O)CC1=CCC1C2CCC2(C)C(O)CCC12
CHEBI
Copy JSON
Description
▾
Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
About this model
Loading…
stable oxygenation
Loading…
unstable oxygenation
Loading…
dehydrogenation
Loading…
reduction
Loading…
hydrolysis
Generation 1
Show metabolites
(1<i>r</i>,2<i>s</i>,3a<i>s</i>,3b<i>r</i>,7<i>r</i>,9a<i>r</i>,9b<i>s</i>,11a<i>s</i>)-9a,11a-dimethyl-2,3,3a,3b,4,6,7,8,9,9a,9b,10,11,11a-tetradecahydro-1<em>h</em>-cyclopenta[<em>a</em>]phenanthrene-1,2,7-triol
CC12CCC(O)CC1=CCC1C2CCC2(C)C(O)C(O)CC12
CHEBI
Copy JSON
Description
▾
Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
i
About this model
Loading…
Generation 2
Show metabolites
CC12CCC3C(CC4OC45CC(O)CCC35C)C1CC(O)C2O
Copy JSON
epoxidation · 0.37
Phase 1
Reactivity
Epoxidation
Quinonation
N-Dealkylation
UGT Conjugation
Loading…