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Submission id: UF423804

Outputs for Genistein; LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+


Database: Department of Effect-Directed Analysis, Helmholtz Centre for Environmental Research - UFZ GmbH, Leipzig, Germany
Entry ID: UF423804
Synonyms: Genistein, 5,7-Dihydroxy-3-(4-hydroxyphenyl)chromen-4-one
Total mass: 270.2365
Formula: H10 C15 O5

Experimental information


MS type: MS2
Instrument: LTQ Orbitrap XL Thermo Scientific
Instrument type: LC-ESI-ITFT
Ionization: ESI
Ionization mode: POSITIVE

CAMP general report:

Acceptable mass threshold: 2.0158
Out of range queried mass peaks:
Replicated queried mass peaks: 91.0539, 111.0075, 121.0283, 133.0283, 133.0647, 147.0438, 149.0231, 159.0438, 175.0748, 183.0437, 187.0388, 187.0751, 201.0545, 226.0617, 227.07,
Processing time: 0:00:06.159707

Results for the quried mass "115.0541"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C8O1 0.055 3 0 C2,C4,C7,C8,C11,C13,C14,C15,O20
C8O1 0.055 3 0 C2,C4,C6,C7,C8,C10,C11,C13,O20
C8O1 0.055 3 0 C2,C4,C7,C8,C11,C12,C13,C14,O20
C8O1 0.055 3 0 C1,C3,C4,C7,C8,C9,C11,C13,O20
C8O1 0.055 3 0 C1,C2,C3,C4,C7,C8,C9,C11,O20
C8O1 0.055 3 0 C1,C2,C3,C4,C8,C9,C11,C15,O19
C8O1 0.055 3 0 C1,C2,C3,C4,C7,C8,C9,C11,O16
C8O1 0.055 3 0 C1,C2,C3,C4,C8,C9,C11,C15,O16
C8O1 0.055 3 0 C1,C3,C4,C7,C8,C9,C11,C15,O19
C8O1 0.055 3 0 C1,C3,C4,C7,C8,C9,C11,C15,O20
C8O1 0.055 3 0 C1,C3,C4,C8,C9,C11,C14,C15,O19
C8O1 0.055 3 0 C1,C3,C4,C8,C9,C11,C14,C15,O16
C8O1 0.055 3 0 C2,C4,C5,C8,C11,C12,C14,C15,O18
C8O1 0.055 3 0 C2,C4,C5,C8,C11,C12,C14,C15,O19
C8O1 0.055 3 0 C2,C4,C6,C7,C8,C11,C13,C14,O20
C8O1 0.055 3 0 C2,C4,C6,C7,C8,C11,C13,C15,O20
C8O1 0.055 3 0 C2,C4,C6,C7,C8,C9,C11,C13,O20
C8O1 0.055 3 0 C2,C4,C6,C8,C11,C13,C14,C15,O20
C8O1 0.055 3 0 C2,C4,C6,C8,C11,C13,C14,C15,O19
C8O1 0.055 3 0 C2,C4,C7,C8,C11,C12,C14,C15,O18
C8O1 0.055 3 0 C2,C4,C7,C8,C9,C11,C13,C14,O20
C8O1 0.055 3 0 C2,C4,C7,C8,C11,C12,C14,C15,O20
C8O1 0.055 3 1 C2,C4,C8,C11,C12,C13,C14,C15,O20
C8O1 0.055 3 0 C2,C4,C8,C9,C11,C12,C14,C15,O16
C8O1 0.055 3 0 C2,C4,C8,C11,C12,C13,C14,C15,O18
C8O1 0.055 3 0 C2,C4,C8,C9,C11,C12,C14,C15,O18
C8O1 0.055 3 0 C2,C4,C8,C9,C11,C13,C14,C15,O16
C8O1 0.055 3 1 C2,C4,C8,C9,C11,C13,C14,C15,O20
C8O1 0.055 3 0 C1,C3,C4,C7,C8,C9,C11,C15,O16
C8O1 0.055 3 0 C2,C4,C7,C8,C9,C11,C13,C15,O20
C8O1 0.055 3 0 C2,C4,C7,C8,C9,C11,C14,C15,O16
C8O1 0.055 3 0 C2,C4,C7,C8,C9,C11,C14,C15,O20
C8O1 0.055 3 0 C2,C4,C7,C8,C11,C12,C14,C15,O19
C8O1 0.055 3 0 C2,C4,C7,C8,C11,C13,C14,C15,O19
C8O1 0.055 3 1 C2,C4,C8,C9,C11,C12,C14,C15,O19
C8O1 0.055 3 1 C2,C4,C8,C9,C11,C13,C14,C15,O19
C8O1 0.055 3 1 C2,C4,C8,C11,C12,C13,C14,C15,O19
C8O1 0.055 3 0 C2,C4,C7,C8,C9,C11,C14,C15,O19
C8O1 0.055 3 0 C1,C3,C7,C8,C9,C11,C13,C14,O20
C8O1 0.055 3 0 C1,C3,C8,C9,C11,C12,C14,C15,O18
C8O1 0.055 3 1 C1,C3,C8,C9,C11,C13,C14,C15,O20
C8O1 0.055 3 0 C1,C3,C7,C8,C9,C11,C13,C15,O20
C8O1 0.055 3 0 C1,C3,C7,C8,C9,C11,C14,C15,O20
C8O1 0.055 3 1 C1,C3,C8,C9,C11,C12,C14,C15,O19
C8O1 0.055 3 0 C1,C3,C8,C9,C11,C12,C14,C15,O16
C8O1 0.055 3 1 C1,C3,C8,C9,C11,C13,C14,C15,O19
C8O1 0.055 3 0 C1,C3,C8,C9,C11,C13,C14,C15,O16
C9 0.097 7 2 C1,C2,C3,C4,C7,C8,C9,C11,C15
C7O2 0.012 1 0 C1,C3,C4,C7,C8,C9,C11,O16,O20
C7O2 0.012 1 0 C1,C3,C4,C8,C9,C11,C15,O16,O19
C7O2 0.012 1 0 C2,C4,C7,C8,C11,C13,C15,O19,O20
C7O2 0.012 1 0 C2,C4,C7,C8,C9,C11,C13,O16,O20
C7O2 0.012 1 0 C2,C4,C8,C11,C12,C14,C15,O18,O19
C7O2 0.012 1 0 C2,C4,C8,C11,C13,C14,C15,O19,O20
C7O2 0.012 1 0 C2,C4,C7,C8,C9,C11,C15,O16,O19
C7O2 0.012 1 0 C2,C4,C7,C8,C9,C11,C15,O16,O20
C7O2 0.012 1 0 C2,C4,C7,C8,C9,C11,C15,O19,O20
C7O2 0.012 1 0 C2,C4,C7,C8,C11,C14,C15,O19,O20
C7O2 0.012 1 0 C2,C4,C8,C9,C11,C14,C15,O16,O19
C7O2 0.012 1 0 C1,C3,C7,C8,C9,C11,C13,O16,O20
C7O2 0.012 1 0 C1,C3,C7,C8,C9,C11,C15,O19,O20
C7O2 0.012 1 0 C1,C3,C7,C8,C9,C11,C15,O16,O20
C7O2 0.012 1 0 C1,C3,C8,C9,C11,C14,C15,O16,O19
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