XenoSite

Batzelladine a

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Batzelladine a Epoxidation prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)N5CCCC5=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 N-Dealkylation prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)NC(CCC(=O)O)=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 stable oxygenation prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)NC(CCC(=O)O)=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 unstable oxygenation prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)NC(CCC(=O)O)=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 dehydrogenation prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)NC(CCC(=O)O)=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 reduction prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)NC(CCC(=O)O)=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 hydrolysis prediction
hydrolysis · 0.51
N=C(N)NCCCCOC(=O)C1=C(CCC(=O)O)NC2(NO2)NC1CCCCCCCCCO
Probability scale from 0.0 to 1.0