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 stable oxygenation prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)N5CCCC5=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 unstable oxygenation prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)N5CCCC5=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 dehydrogenation prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)N5CCCC5=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 reduction prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)N5CCCC5=C4C(=O)OCCCCNC(=N)N)C(C)N=C(N1)N23 hydrolysis prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)N5CCCC5=C4C=O)C(C)N=C(N1)N23 gsh prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)N5CCCC5=C4C=O)C(C)N=C(N1)N23 protein prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)N5CCCC5=C4C=O)C(C)N=C(N1)N23 cyanide prediction
CCCCCCCCCC1CC2CCC3C(C(=O)OCCCCCCCCCC4NC5(NO5)N5CCCC5=C4C=O)C(C)N=C(N1)N23 dna prediction
cyanide · 0.00
*C(O)C1=C2CCCN2C2(NO2)NC1CCCCCCCCCOC(=O)C1C(C)N=C2NC(CCCCCCCCC)CC3CCC1N23 |$CN;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;$|
Probability scale from 0.0 to 1.0