Mass Formula Description
57.034 74.0004 76.016 83.0523 124.9794 1 2 5 3 4 1 77 -90.0470 -C7H6 Benzyl loss
Relative Neutralized Sum of 0 0 0 0 0 1 2 5 4 3 1 2 -56.0626 -C4H8 Loss of butylene
Intensities Fragment Masses Subfragments 0 74.0004 0 83.0523 124.9794 1 3 4 2 5 3 -43.9495 Br -> Cl Bromine to chlorine
0.0000 0 0 0 0 0 1 3 5 4 2 2 -42.0470 -C3H6 Depropylation
0.0000 0 0 0 0 0 1 4 2 3 5 2 -42.0106 -C2H2O Deacetylation
0.0000 0 0 76.016 83.0523 0 1 4 5 3 2 3 -29.9742 NO2 -> NH2 N-reduction (nitro group)
3 74.0005 74.0004 0 0 0 0 0 1 5 2 3 4 2 -28.0313 -C2H4 loss of ethylene
100 76.0161 76.0160 0 0 76.016 0 0 1 5 4 2 3 3 -17.9661 Cl -> OH substitution of OH for Cl
1 158.0606 0.0000 0 74.0004 0 0 0 5 1 3 2 4 3 -15.9949 -O Reduction
11 159.0684 159.0683 5 1 4 2 3 3 -14.0157 -CH2 Demethylation
3 254.0374 0.0000 -2.0157 -H2 Dehydrogenation
1 255.0454 0.0000 -1.0316 CH4N -> CHO Oxidative Deamination
1 282.0323 282.0321 2.0157 +H2 Hydrogenation
5 283.0400 0.0000 4.0313 +2H2 2x Hydrogenation
0 415.0823 415.0821 C3H5O C2H2O3 C5H2N C5H7O C6H2OCl C21H18NO6Cl 1.11 26 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
  57.0340 74.0004 83.0523 124.9794 76.0160 415 31.9898 +O2 2x Oxidation
  0.0000 0.0000 0.0000 0.0000 0.0000 0 42.0106 +C2H2O Acetylation (DMAc solvent)
Partition Score   0.0000 74.0004 83.0523 124.9794 0.0000 282 42.0470 +C3H6 addition of a propyl group
  0.0000 0.0000 0.0000 0.0000 0.0000 0 43.9495 Cl -> Br Chlorine to Bromine substitution
60   0.0000 0.0000 0.0000 0.0000 0.0000 0 57.0215 C2H3NO Glycine conjugate formation
  0.0000 0.0000 83.0523 0.0000 76.0160 159 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
  0.0000 0.0000 0.0000 0.0000 76.0160 76 79.9663 +PO3H Phosphate ester formation
subfragments 5   0.0000 74.0004 0.0000 0.0000 0.0000 74 86.0368 +C4H6O2 butyrolactone addition (NMP solvent)
partition number 21             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 Many Alignments Possible   163.0303 +C5H9NO3S Acetylcysteine addition
100  24  36  8 176.0321 +C6H8O6 Glucuronidation
100  24  36  8 1.11 26 C3H5O C2H2O3 C5H7O C6H2OCl C5H2N C21H18NO6Cl 192.0270 +C6H8O7 Oxidation + Glucuronidation
307.0838 +C10H17N3O6S Glutathione addition
323.0787 +C10H17N3O7S Oxidation + Glutathione addition