Mass Formula Description
24.9952 27.0108 152.0624 218.0935 1 3 2 4 2 3 -90.0470 -C7H6 Benzyl loss
Relative Neutralized Sum of 24.9952 27.0108 152.0624 0 3 1 2 4 2 1 -56.0626 -C4H8 Loss of butylene
Intensities Fragment Masses Subfragments 0 0 0 0 4 3 2 1 3 -43.9495 Br -> Cl Bromine to chlorine
67 151.0547 0.0000 0 0 0 0 -42.0470 -C3H6 Depropylation
17 152.0625 152.0624 0 27.0108 152.0624 0 -42.0106 -C2H2O Deacetylation
18 162.0469 0.0000 0 0 0 0 -29.9742 NO2 -> NH2 N-reduction (nitro group)
36 164.0625 0.0000 24.9952 0 152.0624 0 -28.0313 -C2H4 loss of ethylene
22 168.0574 0.0000 0 0 0 0 -17.9661 Cl -> OH substitution of OH for Cl
20 177.0578 177.0576 0 0 0 0 -15.9949 -O Reduction
33 178.0655 0.0000 0 0 0 0 -14.0157 -CH2 Demethylation
31 179.0734 179.0732 0 0 152.0624 0 -2.0157 -H2 Dehydrogenation
33 189.0577 0.0000 0 0 0 0 -1.0316 CH4N -> CHO Oxidative Deamination
22 191.0608 0.0000 2.0157 +H2 Hydrogenation
100 204.0687 204.0684 4.0313 +2H2 2x Hydrogenation
0 422.1622 422.1619 CH-1N CHN C12H8 C8H15N4OCl C22H23N6OCl CH-1N CHN C12H8 C8H15N4OCl 0.13 50 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 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
  24.9952 152.0624 27.0108 218.0935   422 31.9898 +O2 2x Oxidation
  24.9952 152.0624 27.0108 0.0000   204 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 0.0000 0.0000   0 43.9495 Cl -> Br Chlorine to Bromine substitution
30   0.0000 152.0624 27.0108 0.0000   179 57.0215 C2H3NO Glycine conjugate formation
  0.0000 0.0000 0.0000 0.0000   0 69.0578 OH -> C4H8NO amidation with morpholine (NMM solvent)
  24.9952 152.0624 0.0000 0.0000   177 79.9568 +SO3 Sulfate ester formation
  0.0000 0.0000 0.0000 0.0000   0 79.9663 +PO3H Phosphate ester formation
subfragments 4   0.0000 0.0000 0.0000 0.0000   0 86.0368 +C4H6O2 butyrolactone addition (NMP solvent)
partition number 5   0.0000 0.0000 0.0000 0.0000   0 90.0470 C7H6 Benzyl group addition
  0.0000 152.0624 0.0000 0.0000   152 107.0041 +C2H5NO2S Taurine Conjugation
  0.0000 0.0000 0.0000 0.0000   0 162.0164 +C5H6O6 Demethylation + Glucuronidation
Isotope Ratios Avg SubFrag MassError Relative Feasibility Linear Alignment of SubFragments   163.0303 +C5H9NO3S Acetylcysteine addition
100  26  36  9 176.0321 +C6H8O6 Glucuronidation
100  26  36  9 0.13 50 CH-1N C12H8 CHN C8H15N4OCl C22H23N6OCl 192.0270 +C6H8O7 Oxidation + Glucuronidation
307.0838 +C10H17N3O6S Glutathione addition
323.0787 +C10H17N3O7S Oxidation + Glutathione addition