Mass Formula Description
18.0106 28.0312 28.0312 77.933 196.92 2 1 4 3 5 4 3 -90.0470 -C7H6 Benzyl loss
Relative Neutralized Sum of
18.0106 0 28.0312 77.933 196.92 3 1 5 2 4 2 3 -56.0626 -C4H8 Loss of butylene
Intensities Fragment Masses Subfragments 18.0106 0 0 77.933 196.92 3 5 1 2 4 3 -43.9495 Br -> Cl Bromine to chlorine
36 95.9434 95.9436 0 0 0 77.933 196.92 5 4 3 2 1 4 -42.0470 -C3H6 Depropylation
57 113.9540 0.0000 0 0 0 0 0 -42.0106 -C2H2O Deacetylation
15 123.9748 123.9748 0 0 0 0 196.92 -29.9742 NO2 -> NH2 N-reduction (nitro group)
4 141.9854 0.0000 0 0 0 0 0 -28.0313 -C2H4 loss of ethylene
4 152.0061 152.0060 18.0106 28.0312 28.0312 77.933 0 -17.9661 Cl -> OH substitution of OH for Cl
5 170.0167 0.0000 0 0 0 0 0 -15.9949 -O Reduction
100 196.9201 196.9200 18.0106 28.0312 0 77.933 0 -14.0157 -CH2 Demethylation
5 212.8973 0.0000 0 0 0 0 0 -2.0157 -H2 Dehydrogenation
3 274.8531 274.8530 18.0106 0 0 77.933 0 -1.0316 CH4N -> CHO Oxidative Deamination
32 292.8637 292.8636 2.0157 +H2 Hydrogenation
8 320.8949 320.8948 4.0313 +2H2 2x Hydrogenation
0 348.9259 348.9260 H2O C2H4 C2H4 H-1OSP C5H2NOCl3 C9H11NO3SPCl3 0.14 7 13.9793 CH2OH -> COOH Oxidation of alcohols
H2O C2H4 C2H4 H-1OSP C5N3OBr C9H9N3O3SPBr 0.56 2 14.0157 +CH2 Methylation
15.9949 +O Oxidation
18.0106 +H2O Hydrolysis of cyclic amides and esters
Alignment of SubFragments 1 27.9949 RNH2 -> RNH-HC=O Formylation (DMF solvent)
SubFrag 1 SubFrag 2 SubFrag 3 SubFrag 4 SubFrag 5 28.0313 +C2H4 addition of ethyl 
Delta
 
          S 29.9742 CH3 -> COOH Methyl group oxidation to acid
  28.0312 18.0106 77.9330 28.0312 196.9200 349 31.9898 +O2 2x Oxidation
  0.0000 18.0106 77.9330 28.0312 196.9200 321 42.0106 +C2H2O Acetylation (DMAc solvent)
Partition Score   0.0000 18.0106 77.9330 0.0000 196.9200 293 42.0470 +C3H6 addition of a propyl group
  0.0000 0.0000 77.9330 0.0000 196.9200 275 43.9495 Cl -> Br Chlorine to Bromine substitution
67   0.0000 0.0000 0.0000 0.0000 0.0000 0 57.0215 C2H3NO Glycine conjugate formation
  0.0000 0.0000 0.0000 0.0000 196.9200 197 69.0578 OH -> C4H8NO amidation with morpholine (NMM solvent)
  0.0000 0.0000 0.0000 0.0000 0.0000 0 79.9568 +SO3 Sulfate ester formation
  28.0312 18.0106 77.9330 28.0312 0.0000 152 79.9663 +PO3H Phosphate ester formation
subfragments 5   0.0000 0.0000 0.0000 0.0000 0.0000 0 86.0368 +C4H6O2 butyrolactone addition (NMP solvent)
  28.0312 18.0106 77.9330 0.0000 0.0000 124 90.0470 C7H6 Benzyl group addition
  0.0000 0.0000 0.0000 0.0000 0.0000 0 107.0041 +C2H5NO2S Taurine Conjugation
  0.0000 18.0106 77.9330 0.0000 0.0000 96 162.0164 +C5H6O6 Demethylation + Glucuronidation
Isotope Ratios Avg SubFrag MassError Relative Feasibility  All Connected to White, but SF5 to SF3   163.0303 +C5H9NO3S Acetylcysteine addition
100  8  96  8 176.0321 +C6H8O6 Glucuronidation
99  11  100  11 0.14 7 C2H4 H2O H-1OSP C2H4 C5H2NOCl3 C9H11NO3SPCl3 192.0270 +C6H8O7 Oxidation + Glucuronidation
97  12  100  12 0.56 2 C2H4 H2O H-1OSP C2H4 C5N3OBr C9H9N3O3SPBr 307.0838 +C10H17N3O6S Glutathione addition
323.0787 +C10H17N3O7S Oxidation + Glutathione addition