XenoSite

Action

CHEBI
Phase 1ReactivityEpoxidationQuinonationN-DealkylationUGT Conjugation
Action stable oxygenation prediction
Action unstable oxygenation prediction
Action dehydrogenation prediction
Action reduction prediction
Action hydrolysis prediction

2-[[2-chloro-4-fluoro-5-[(tetrahydro-3-oxo-1<em>h</em>,3<em>h</em>-[1,3,4]thiadiazolo[3,4-<em>a</em>]pyridazin-1-ylidene)amino]phenyl]thio]acetic acid

CHEBI
2-[[2-chloro-4-fluoro-5-[(tetrahydro-3-oxo-1<em>h</em>,3<em>h</em>-[1,3,4]thiadiazolo[3,4-<em>a</em>]pyridazin-1-ylidene)amino]phenyl]thio]acetic acid gsh prediction
2-[[2-chloro-4-fluoro-5-[(tetrahydro-3-oxo-1<em>h</em>,3<em>h</em>-[1,3,4]thiadiazolo[3,4-<em>a</em>]pyridazin-1-ylidene)amino]phenyl]thio]acetic acid protein prediction
2-[[2-chloro-4-fluoro-5-[(tetrahydro-3-oxo-1<em>h</em>,3<em>h</em>-[1,3,4]thiadiazolo[3,4-<em>a</em>]pyridazin-1-ylidene)amino]phenyl]thio]acetic acid cyanide prediction
2-[[2-chloro-4-fluoro-5-[(tetrahydro-3-oxo-1<em>h</em>,3<em>h</em>-[1,3,4]thiadiazolo[3,4-<em>a</em>]pyridazin-1-ylidene)amino]phenyl]thio]acetic acid dna prediction
glutathionation · 0.03
*c1cc(F)c(N=c2sc(=O)n3n2CCCC3)cc1SCC(=O)O |$GSH;;;;;;;;;;;;;;;;;;;;;;;$|
Probability scale from 0.0 to 1.0