Mass Formula Description
17.0264 30.0218 88.0314 90.0468 1 3 2 4 2 1 -90.0470 -C7H6 Benzyl loss
Relative Neutralized Sum of 0 30.0218 88.0314 90.0468 1 -56.0626 -C4H8 Loss of butylene
Intensities Fragment Masses Subfragments 0 0 0 0 -43.9495 Br -> Cl Bromine to chlorine
0.0000 0 30.0218 0 90.0468 -42.0470 -C3H6 Depropylation
0.0000 0 0 0 0 -42.0106 -C2H2O Deacetylation
0.0000 0 30.0218 88.0314 0 -29.9742 NO2 -> NH2 N-reduction (nitro group)
18 90.0469 90.0468 0 0 0 0 -28.0313 -C2H4 loss of ethylene
35 105.0579 105.0578 17.0264 0 88.0314 0 -17.9661 Cl -> OH substitution of OH for Cl
24 108.0576 0.0000 0 0 0 90.0468 -15.9949 -O Reduction
18 118.0532 118.0532 -14.0157 -CH2 Demethylation
6 119.0735 0.0000 -2.0157 -H2 Dehydrogenation
29 120.0688 120.0686 -1.0316 CH4N -> CHO Oxidative Deamination
18 132.0688 0.0000 2.0157 +H2 Hydrogenation
100 208.1002 208.1000 4.0313 +2H2 2x Hydrogenation
0 225.1266 225.1264 H3N H2N2 C7H4 C7H6 C14H15N3 H3N H2N2 C7H4 C7H6 0.13 213 13.9793 CH2OH -> COOH Oxidation of alcohols
14.0157 +CH2 Methylation
15.9949 +O Oxidation
18.0106 +H2O Hydrolysis of cyclic amides and esters
Alignment of SubFragments 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
  17.0264 88.0314 30.0218 90.0468   225 31.9898 +O2 2x Oxidation
  0.0000 88.0314 30.0218 90.0468   208 42.0106 +C2H2O Acetylation (DMAc solvent)
Partition Score   0.0000 0.0000 0.0000 0.0000   0 42.0470 +C3H6 addition of a propyl group
  0.0000 0.0000 30.0218 90.0468   120 43.9495 Cl -> Br Chlorine to Bromine substitution
77   0.0000 0.0000 0.0000 0.0000   0 57.0215 C2H3NO Glycine conjugate formation
  0.0000 88.0314 30.0218 0.0000   118 69.0578 OH -> C4H8NO amidation with morpholine (NMM solvent)
  0.0000 0.0000 0.0000 0.0000   0 79.9568 +SO3 Sulfate ester formation
  17.0264 88.0314 0.0000 0.0000   105 79.9663 +PO3H Phosphate ester formation
subfragments 4   0.0000 0.0000 0.0000 90.0468   90 86.0368 +C4H6O2 butyrolactone addition (NMP solvent)
partition number 1             0 90.0470 C7H6 Benzyl group addition
            0 107.0041 +C2H5NO2S Taurine Conjugation
            0 162.0164 +C5H6O6 Demethylation + Glucuronidation
Isotope Ratios Avg SubFrag MassError Relative Feasibility Linear Alignment of SubFragments   163.0303 +C5H9NO3S Acetylcysteine addition
100  16  1  0 176.0321 +C6H8O6 Glucuronidation
100  16  1  0 0.13 213 H3N C7H4 H2N2 C7H6 C14H15N3 192.0270 +C6H8O7 Oxidation + Glucuronidation
307.0838 +C10H17N3O6S Glutathione addition
323.0787 +C10H17N3O7S Oxidation + Glutathione addition