NMRFAM Logo Computational Annotation of MS Peaks (CAMP)
Home
Processed databases
Atom-Mass pairs

Search:
(Search for compound name or MassBank ID)

Submission id: KO009017

Outputs for Kynurenine; LC-ESI-IT; MS3; m/z: 209/192; [M+H]+


Database: Institute for Advanced Biosciences, Keio Univ.
Entry ID: KO009017
Synonyms: Kynurenine, 3-Anthraniloyl-L-alanine, L-Kynurenine
Total mass: 208.2134
Formula: H12 C10 O3 N2

Experimental information


MS type: MS3
Instrument: LC/MSD Trap XCT, Agilent Technologies
Instrument type: LC-ESI-IT
Ionization mode: POSITIVE

CAMP general report:

Acceptable mass threshold: 2.0158
Out of range queried mass peaks: 214.1,219.2,228.9,232.4,
Replicated queried mass peaks: 95.0, 100.1, 115.1, 118.1, 136.1, 146.9, 150.0, 151.0, 164.0, 174.0, 175.2,
Processing time: 0:00:02.996599

Results for the quried mass "88.1"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C3O2N1 0.015 6 0 C5,C8,C10,N12,O14,O15
C6O1 0.036 0 0 C1,C2,C4,C6,C7,C9,O13
C6O1 0.036 0 0 C1,C2,C3,C4,C6,C9,O13
C6O1 0.036 0 0 C1,C3,C4,C6,C7,C9,O13
C6O1 0.036 0 0 C1,C3,C5,C6,C8,C9,O13
C6O1 0.036 0 0 C1,C2,C3,C5,C6,C9,O13
C6O1 0.036 0 0 C1,C2,C3,C6,C7,C9,O13
C6O1 0.036 0 0 C1,C3,C5,C6,C7,C9,O13
C6O1 0.036 0 0 C2,C3,C4,C6,C7,C9,O13
C6O1 0.036 0 0 C2,C4,C5,C6,C7,C9,O13
C6O1 0.036 0 0 C3,C5,C6,C8,C9,C10,O14
C6O1 0.036 0 0 C3,C5,C6,C8,C9,C10,O15
C6O1 0.036 0 0 C3,C5,C6,C8,C9,C10,O13
C6O1 0.036 0 0 C3,C4,C5,C6,C7,C9,O13
C6O1 0.036 0 0 C3,C5,C6,C7,C8,C9,O13
C6O1 0.036 0 0 C4,C5,C6,C7,C8,C9,O13
C6O1 0.036 0 0 C5,C6,C7,C8,C9,C10,O14
C6O1 0.036 0 0 C5,C6,C7,C8,C9,C10,O15
C6O1 0.036 0 0 C5,C6,C7,C8,C9,C10,O13
C6N1 0.013 2 0 C1,C3,C5,C6,C8,C9,N12
C6N1 0.013 2 0 C1,C2,C3,C4,C6,C7,N11
C6N1 0.013 2 0 C1,C2,C4,C6,C7,C9,N11
C6N1 0.013 2 0 C1,C3,C5,C6,C7,C9,N11
C6N1 0.013 2 0 C1,C2,C3,C6,C7,C9,N11
C6N1 0.013 2 0 C1,C3,C4,C6,C7,C9,N11
C6N1 0.013 2 0 C2,C4,C5,C6,C7,C9,N11
C6N1 0.013 2 0 C2,C3,C4,C6,C7,C9,N11
C6N1 0.013 2 0 C3,C5,C6,C7,C8,C9,N11
C6N1 0.013 2 0 C3,C5,C6,C8,C9,C10,N12
C6N1 0.013 2 0 C3,C5,C6,C7,C8,C9,N12
C6N1 0.013 2 0 C3,C4,C5,C6,C7,C9,N11
C6N1 0.013 2 0 C4,C5,C6,C7,C8,C9,N12
C6N1 0.013 2 0 C4,C5,C6,C7,C8,C9,N11
C6N1 0.013 2 0 C5,C6,C7,C8,C9,C10,N11
C6N1 0.013 2 0 C5,C6,C7,C8,C9,C10,N12
C5N2 0.033 0 0 C5,C6,C7,C8,C9,N11,N12
C7 0.007 4 0 C1,C2,C4,C5,C6,C7,C9
C7 0.007 4 0 C1,C3,C5,C6,C8,C9,C10
C7 0.007 4 0 C1,C2,C3,C5,C6,C8,C9
C7 0.007 4 0 C1,C2,C3,C4,C6,C7,C9
C7 0.007 4 0 C1,C2,C3,C4,C5,C6,C9
C7 0.007 4 0 C1,C3,C4,C5,C6,C7,C9
C7 0.007 4 0 C1,C3,C5,C6,C7,C8,C9
C7 0.007 4 0 C1,C2,C3,C5,C6,C7,C9
C7 0.007 4 0 C2,C4,C5,C6,C7,C8,C9
C7 0.007 4 0 C2,C3,C4,C5,C6,C7,C9
C7 0.007 4 0 C3,C4,C5,C6,C7,C8,C9
C7 0.007 4 0 C3,C5,C6,C7,C8,C9,C10
C7 0.007 4 0 C4,C5,C6,C7,C8,C9,C10
C5O1N1 0.056 2 0 C1,C3,C6,C7,C9,N11,O13
C5O1N1 0.056 2 0 C2,C4,C6,C7,C9,N11,O13
C5O1N1 0.056 2 0 C3,C5,C6,C8,C9,N12,O13
C5O1N1 0.056 2 0 C3,C4,C6,C7,C9,N11,O13
C5O1N1 0.056 2 0 C3,C5,C6,C7,C9,N11,O13
C5O1N1 0.056 2 0 C4,C5,C6,C7,C9,N11,O13
C5O1N1 0.056 2 0 C5,C6,C7,C8,C9,N11,O13
C5O1N1 0.056 2 0 C5,C6,C7,C8,C9,N12,O13
C5O1N1 0.056 2 0 C5,C6,C8,C9,C10,N12,O14
C5O1N1 0.056 2 0 C5,C6,C8,C9,C10,N12,O15
C5O1N1 0.056 2 0 C5,C6,C8,C9,C10,N12,O13
Flag Counter