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Submission id: BML01832

Outputs for 3,4-Dihydroxy-L-phenylalanine; LC-ESI-QTOF; MS2; CE 10 ev; [M-H]-


Database: Institute of Biological Chemistry, Washington State University
Entry ID: BML01832
Synonyms: 3,4-Dihydroxy-L-phenylalanine
Total mass: 197.1875
Formula: H11 C9 O4 N1

Experimental information


MS type: MS2
Instrument: Agilent 1200 RRLC; Agilent 6520 QTOF
Instrument type: LC-ESI-QTOF
Ionization mode: NEGATIVE

CAMP general report:

Acceptable mass threshold: 2.0158
Out of range queried mass peaks:
Replicated queried mass peaks: 108.0464, 109.0296, 122.0371, 134.067, 135.0442, 135.0751, 135.0958, 179.0737, 179.1006, 195.8084, 195.8395, 196.0237, 196.061,
Processing time: 0:00:01.968110

Results for the quried mass "101.7069"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C7N1 0.406 4 0 C1,C2,C3,C5,C6,C7,C8,N10
C7N1 0.406 4 0 C1,C2,C3,C5,C6,C7,C9,N10
C7N1 0.406 4 0 C3,C4,C5,C6,C7,C8,C9,N10
C7N1 0.406 4 0 C1,C3,C4,C5,C6,C7,C8,N10
C7N1 0.406 4 0 C2,C3,C4,C5,C6,C7,C8,N10
C7N1 0.406 4 0 C1,C2,C3,C4,C5,C6,C8,N10
C7N1 0.406 4 0 C1,C2,C3,C4,C5,C6,C7,N10
C7O1 0.383 2 0 C1,C2,C3,C5,C6,C7,C9,O13
C7O1 0.383 2 0 C1,C2,C3,C5,C6,C7,C9,O14
C7O1 0.383 2 0 C1,C2,C3,C5,C6,C7,C8,O12
C7O1 0.383 2 0 C1,C2,C3,C5,C6,C7,C9,O11
C7O1 0.383 2 0 C3,C4,C5,C6,C7,C8,C9,O11
C7O1 0.383 2 0 C3,C4,C5,C6,C7,C8,C9,O13
C7O1 0.383 2 0 C3,C4,C5,C6,C7,C8,C9,O14
C7O1 0.383 2 0 C1,C2,C3,C5,C6,C7,C8,O11
C7O1 0.383 2 0 C3,C4,C5,C6,C7,C8,C9,O12
C7O1 0.383 2 0 C1,C2,C3,C4,C5,C7,C8,O12
C7O1 0.383 2 0 C1,C2,C3,C4,C5,C7,C8,O11
C7O1 0.383 2 0 C1,C3,C4,C5,C6,C7,C8,O11
C7O1 0.383 2 0 C1,C3,C4,C5,C6,C8,C9,O12
C7O1 0.383 2 0 C1,C3,C4,C5,C6,C8,C9,O13
C7O1 0.383 2 0 C1,C3,C4,C5,C6,C8,C9,O14
C7O1 0.383 2 0 C1,C2,C3,C4,C5,C6,C8,O12
C7O1 0.383 2 0 C1,C2,C3,C4,C5,C6,C9,O13
C7O1 0.383 2 0 C1,C2,C3,C4,C5,C6,C9,O14
C7O1 0.383 2 0 C2,C3,C4,C5,C6,C7,C8,O12
C7O1 0.383 2 0 C2,C3,C4,C5,C6,C7,C8,O11
C7O1 0.383 2 0 C1,C2,C3,C4,C5,C6,C7,O11
C8 0.426 6 1 C1,C2,C3,C5,C6,C7,C8,C9
C8 0.426 6 0 C1,C2,C3,C4,C5,C6,C7,C8
C8 0.426 6 1 C1,C3,C4,C5,C6,C7,C8,C9
C8 0.426 6 1 C2,C3,C4,C5,C6,C7,C8,C9
C8 0.426 6 0 C1,C2,C3,C4,C5,C6,C8,C9
C8 0.426 6 0 C1,C2,C3,C4,C5,C6,C7,C9
C6O1N1 0.363 0 0 C1,C2,C3,C5,C6,C7,N10,O11
C6O1N1 0.363 0 0 C3,C4,C5,C6,C7,C8,N10,O11
C6O1N1 0.363 0 0 C3,C4,C5,C6,C7,C8,N10,O12
C6O1N1 0.363 0 0 C3,C4,C5,C6,C8,C9,N10,O13
C6O1N1 0.363 0 0 C3,C4,C5,C6,C8,C9,N10,O14
C6O1N1 0.363 0 0 C3,C4,C5,C6,C8,C9,N10,O12
C6O1N1 0.363 0 0 C1,C3,C4,C5,C6,C8,N10,O12
C6O1N1 0.363 0 0 C1,C2,C3,C5,C6,C9,N10,O13
C6O1N1 0.363 0 0 C1,C2,C3,C5,C6,C9,N10,O14
C4O2N1 0.405 8 2 C3,C5,C6,C9,N10,O13,O14
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