Mass Formula Description
27.9948 45.0578 60.0214 132.0576 149.0301 1 4 5 3 2 1 77 -90.0470 -C7H6 Benzyl loss
Relative Neutralized Sum of
27.9948 0 60.0214 132.0576 149.0301 1 5 3 4 2 2 3 -56.0626 -C4H8 Loss of butylene
Intensities Fragment Masses Subfragments 0 0 0 0 0 1 5 4 3 2 2 -43.9495 Br -> Cl Bromine to chlorine
0.0000 27.9948 0 0 132.0576 149.0301 1 5 4 3 2 3 -42.0470 -C3H6 Depropylation
5 71.0735 0.0000 0 0 0 0 0 2 1 4 5 3 3 -42.0106 -C2H2O Deacetylation
2 108.0035 0.0000 27.9948 0 0 0 149.0301 2 1 5 3 4 3 -29.9742 NO2 -> NH2 N-reduction (nitro group)
2 120.0576 0.0000 0 0 0 0 149.0301 2 1 5 4 3 2 -28.0313 -C2H4 loss of ethylene
5 136.0526 0.0000 0 0 0 0 0 2 1 5 4 3 3 -17.9661 Cl -> OH substitution of OH for Cl
21 149.0301 149.0301 0 0 0 0 0 2 5 1 3 4 3 -15.9949 -O Reduction
100 177.0249 177.0249 0 0 0 0 0 2 5 1 4 3 3 -14.0157 -CH2 Demethylation
3 190.0329 0.0000 0 0 0 0 0 -2.0157 -H2 Dehydrogenation
3 309.0825 309.0825 -1.0316 CH4N -> CHO Oxidative Deamination
1 311.0982 0.0000 2.0157 +H2 Hydrogenation
7 369.1039 369.1039 4.0313 +2H2 2x Hydrogenation
0 414.1617 414.1617 CO C2H7N C2H4O2 C9H8O C8H7NS C22H26N2O4S 0.13 296 13.9793 CH2OH -> COOH Oxidation of alcohols
CO C2H7N C2H4O2 C9H8O C4H7NO5 C18H26N2O9 0.57 10 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
  27.9948 149.0301 132.0576 45.0578 60.0214 414 31.9898 +O2 2x Oxidation
  27.9948 149.0301 132.0576 0.0000 60.0214 369 42.0106 +C2H2O Acetylation (DMAc solvent)
Partition Score   0.0000 0.0000 0.0000 0.0000 0.0000 0 42.0470 +C3H6 addition of a propyl group
  27.9948 149.0301 132.0576 0.0000 0.0000 309 43.9495 Cl -> Br Chlorine to Bromine substitution
56   0.0000 0.0000 0.0000 0.0000 0.0000 0 57.0215 C2H3NO Glycine conjugate formation
  27.9948 149.0301 0.0000 0.0000 0.0000 177 69.0578 OH -> C4H8NO amidation with morpholine (NMM solvent)
  0.0000 149.0301 0.0000 0.0000 0.0000 149 79.9568 +SO3 Sulfate ester formation
  0.0000 0.0000 0.0000 0.0000 0.0000 0 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)
  0.0000 0.0000 0.0000 0.0000 0.0000 0 90.0470 C7H6 Benzyl group addition
  0.0000 0.0000 0.0000 0.0000 0.0000 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  22  6  0 176.0321 +C6H8O6 Glucuronidation
100  26  8  2 0.13 296 CO C8H7NS C9H8O C2H7N C2H4O2 C22H26N2O4S 192.0270 +C6H8O7 Oxidation + Glucuronidation
100  21  4  1 0.57 10 CO C4H7NO5 C9H8O C2H7N C2H4O2 C18H26N2O9 307.0838 +C10H17N3O6S Glutathione addition
323.0787 +C10H17N3O7S Oxidation + Glutathione addition