XenoSite

Adipiodone dianion

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Adipiodone dianion Epoxidation prediction
O=C(CCCCC(=O)NC12OC1(I)C(C(=O)[O-])=C(I)C=C2I)Nc1c(I)cc(I)c(C(=O)[O-])c1I stable oxygenation prediction
O=C(CCCCC(=O)NC12OC1(I)C(C(=O)[O-])=C(I)C=C2I)Nc1c(I)cc(I)c(C(=O)[O-])c1I unstable oxygenation prediction
O=C(CCCCC(=O)NC12OC1(I)C(C(=O)[O-])=C(I)C=C2I)Nc1c(I)cc(I)c(C(=O)[O-])c1I dehydrogenation prediction
O=C(CCCCC(=O)NC12OC1(I)C(C(=O)[O-])=C(I)C=C2I)Nc1c(I)cc(I)c(C(=O)[O-])c1I reduction prediction
O=C(CCCCC(=O)NC12OC1(I)C(C(=O)[O-])=C(I)C=C2I)Nc1c(I)cc(I)c(C(=O)[O-])c1I hydrolysis prediction
O=C(O)CCCCC(=O)Nc1c(I)cc(I)c(C(=O)[O-])c1I Quinonation prediction
quinone formation · 0.31
N=C1C(=O)C=C(I)C(C(=O)[O-])=C1I
Probability scale from 0.0 to 1.0