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Submission id: PR040041

Outputs for Naringenin; LC-ESI-QTOF; MS2; CE:Ramp 5-60 eV; [M-H]-


Database: Plant Science Center, RIKEN
Entry ID: PR040041
Synonyms: 4',5,7-trihydroxyflavanone, Naringenin, Nari, (2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)chroman-4-one
Total mass: 272.2523
Formula: H12 C15 O5

Experimental information


MS type: MS2
Instrument: UPLC Q-Tof Premier, Waters
Instrument type: LC-ESI-QTOF
Ionization: ESI
Ionization mode: NEGATIVE

CAMP general report:

Acceptable mass threshold: 2.0158
Out of range queried mass peaks:
Replicated queried mass peaks: 65.0013, 119.0501, 152.0069, 271.2796, 271.3123, 271.753, 272.0655,
Processing time: 0:00:04.211933

Results for the quried mass "120.0534"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C8O1 0.095 8 0 C1,C2,C3,C4,C7,C8,C9,C13,O16
C10 0.054 0 0 C1,C5,C6,C7,C8,C10,C12,C13,C14,C15
C10 0.054 0 0 C1,C5,C6,C7,C8,C10,C11,C12,C13,C15
C10 0.054 0 0 C1,C2,C3,C4,C7,C8,C9,C12,C13,C15
C10 0.054 0 0 C1,C2,C4,C5,C7,C8,C11,C12,C13,C15
C10 0.054 0 0 C1,C2,C4,C6,C7,C8,C12,C13,C14,C15
C10 0.054 0 0 C1,C2,C4,C7,C8,C9,C11,C12,C13,C15
C10 0.054 0 0 C1,C2,C4,C7,C8,C9,C12,C13,C14,C15
C10 0.054 0 0 C1,C2,C5,C7,C8,C10,C11,C12,C13,C15
C10 0.054 0 0 C1,C2,C6,C7,C8,C10,C12,C13,C14,C15
C10 0.054 0 0 C1,C3,C5,C7,C8,C10,C11,C12,C13,C15
C10 0.054 0 0 C1,C3,C6,C7,C8,C10,C12,C13,C14,C15
C10 0.054 0 0 C1,C3,C4,C7,C8,C9,C11,C12,C13,C15
C10 0.054 0 0 C1,C3,C4,C7,C8,C9,C12,C13,C14,C15
C10 0.054 0 0 C1,C3,C5,C7,C8,C9,C11,C12,C13,C15
C10 0.054 0 0 C1,C3,C6,C7,C8,C9,C12,C13,C14,C15
C10 0.054 0 0 C1,C5,C7,C8,C10,C11,C12,C13,C14,C15
C10 0.054 0 0 C1,C5,C6,C7,C8,C11,C12,C13,C14,C15
C10 0.054 0 0 C1,C6,C7,C8,C10,C11,C12,C13,C14,C15
C10 0.054 0 0 C1,C2,C3,C4,C7,C8,C11,C12,C13,C15
C10 0.054 0 0 C1,C2,C3,C4,C7,C8,C12,C13,C14,C15
C10 0.054 0 0 C1,C2,C3,C5,C7,C8,C11,C12,C13,C15
C10 0.054 0 0 C1,C2,C3,C6,C7,C8,C12,C13,C14,C15
C10 0.054 0 0 C1,C2,C3,C7,C8,C9,C11,C12,C13,C15
C10 0.054 0 0 C1,C2,C3,C7,C8,C9,C12,C13,C14,C15
C10 0.054 0 0 C2,C5,C6,C7,C8,C10,C12,C13,C14,C15
C10 0.054 0 0 C2,C5,C6,C7,C8,C10,C11,C12,C13,C15
C10 0.054 0 0 C2,C3,C4,C7,C8,C9,C11,C12,C13,C15
C10 0.054 0 0 C2,C3,C4,C7,C8,C9,C12,C13,C14,C15
C10 0.054 0 0 C2,C4,C5,C7,C8,C10,C11,C12,C13,C15
C10 0.054 0 0 C2,C4,C6,C7,C8,C10,C12,C13,C14,C15
C10 0.054 0 0 C2,C4,C5,C7,C8,C9,C11,C12,C13,C15
C10 0.054 0 0 C2,C4,C6,C7,C8,C9,C12,C13,C14,C15
C10 0.054 0 0 C2,C5,C7,C8,C10,C11,C12,C13,C14,C15
C10 0.054 0 0 C2,C5,C6,C7,C8,C11,C12,C13,C14,C15
C10 0.054 0 0 C2,C6,C7,C8,C10,C11,C12,C13,C14,C15
C10 0.054 0 0 C1,C3,C5,C7,C8,C11,C12,C13,C14,C15
C10 0.054 0 0 C1,C3,C6,C7,C8,C11,C12,C13,C14,C15
C10 0.054 0 0 C2,C4,C5,C7,C8,C11,C12,C13,C14,C15
C10 0.054 0 0 C2,C4,C6,C7,C8,C11,C12,C13,C14,C15
C10 0.054 0 0 C5,C6,C7,C8,C10,C11,C12,C13,C14,C15
C10 0.054 0 0 C1,C3,C7,C8,C9,C11,C12,C13,C14,C15
C10 0.054 0 0 C2,C4,C7,C8,C9,C11,C12,C13,C14,C15
C6O3 0.009 0 0 C5,C7,C10,C11,C12,C15,O17,O18,O19
C6O3 0.009 0 0 C5,C6,C10,C11,C14,C15,O17,O18,O20
C6O3 0.009 0 0 C5,C6,C10,C11,C12,C15,O17,O18,O19
C7O2 0.052 4 0 C1,C2,C3,C4,C8,C9,C13,O16,O20
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