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Atom-Mass pairs
Submission id: EQ326553

Outputs for Genistein; LC-ESI-QFT; MS2; CE: 45; R=35000; [M-H]-


Database: Department of Environmental Chemistry, Eawag
Entry ID: EQ326553
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: Q Exactive Plus Orbitrap Thermo Scientific
Instrument type: LC-ESI-QFT
Ionization: ESI
Ionization mode: NEGATIVE

CAMP general report:

Acceptable mass threshold: 2.0158
Out of range queried mass peaks:
Replicated queried mass peaks: 65.0033, 91.0189, 133.0295, 135.0451, 157.0294, 157.0658, 161.0245, 171.0452, 181.0659, 182.0374, 196.0529, 199.04, 224.0479, 227.0351, 241.0506, 269.0455,
Processing time: 0:00:04.420647

Results for the quried mass "63.024"

FormulaMass differencesNum. used protonsNum. required extra protonsAtom names
C4O1 0.010 1 0 C1,C8,C11,C15,O19
C4O1 0.010 1 0 C1,C7,C8,C11,O20
C4O1 0.010 1 0 C1,C3,C4,C9,O16
C4O1 0.010 1 0 C1,C3,C8,C9,O16
C4O1 0.010 1 0 C2,C8,C11,C15,O19
C4O1 0.010 1 0 C2,C7,C8,C11,O20
C4O1 0.010 1 0 C2,C3,C4,C9,O16
C4O1 0.010 1 0 C2,C4,C8,C9,O16
C4O1 0.010 1 0 C5,C12,C14,C15,O19
C4O1 0.010 1 0 C5,C6,C10,C13,O20
C4O1 0.010 1 0 C5,C12,C13,C14,O20
C4O1 0.010 1 0 C5,C6,C10,C12,O18
C4O1 0.010 1 0 C5,C6,C10,C13,O17
C4O1 0.010 1 0 C5,C10,C12,C14,O17
C4O1 0.010 1 0 C5,C12,C13,C14,O18
C4O1 0.010 1 0 C5,C12,C14,C15,O18
C4O1 0.010 1 0 C5,C6,C10,C12,O17
C4O1 0.010 1 0 C5,C10,C12,C14,O18
C4O1 0.010 1 0 C6,C7,C11,C13,O20
C4O1 0.010 1 0 C6,C12,C13,C14,O18
C4O1 0.010 1 0 C6,C13,C14,C15,O19
C4O1 0.010 1 0 C6,C7,C10,C13,O20
C4O1 0.010 1 0 C6,C7,C13,C14,O20
C4O1 0.010 1 0 C6,C10,C13,C14,O17
C4O1 0.010 1 0 C6,C12,C13,C14,O20
C4O1 0.010 1 0 C6,C13,C14,C15,O20
C4O1 0.010 1 0 C6,C10,C13,C14,O20
C4O1 0.010 1 0 C7,C12,C13,C14,O20
C4O1 0.010 1 0 C7,C13,C14,C15,O20
C4O1 0.010 1 0 C7,C8,C11,C15,O19
C4O1 0.010 1 0 C7,C8,C11,C13,O20
C4O1 0.010 1 0 C7,C11,C13,C14,O20
C4O1 0.010 1 0 C7,C11,C14,C15,O19
C4O1 0.010 1 0 C7,C11,C14,C15,O20
C4O1 0.010 1 0 C7,C11,C13,C15,O20
C4O1 0.010 1 0 C7,C8,C11,C15,O20
C4O1 0.010 1 1 C8,C11,C14,C15,O19
C4O1 0.010 1 0 C11,C12,C14,C15,O18
C4O1 0.010 1 1 C11,C13,C14,C15,O20
C4O1 0.010 1 1 C11,C12,C14,C15,O19
C4O1 0.010 1 1 C11,C13,C14,C15,O19
C4O1 0.010 1 1 C12,C13,C14,C15,O19
C4O1 0.010 1 1 C12,C13,C14,C15,O20
C4O1 0.010 1 0 C12,C13,C14,C15,O18
C5 0.053 3 0 C1,C2,C3,C4,C9
C5 0.053 3 0 C1,C2,C4,C8,C9
C5 0.053 3 2 C1,C8,C11,C14,C15
C5 0.053 3 0 C1,C2,C3,C4,C8
C5 0.053 3 0 C1,C2,C4,C8,C11
C5 0.053 3 0 C1,C2,C3,C8,C9
C5 0.053 3 0 C1,C2,C7,C8,C11
C5 0.053 3 1 C1,C2,C8,C11,C15
C5 0.053 3 0 C1,C3,C7,C8,C11
C5 0.053 3 1 C1,C3,C8,C11,C15
C5 0.053 3 0 C1,C3,C4,C8,C9
C5 0.053 3 1 C1,C3,C8,C9,C11
C5 0.053 3 1 C1,C7,C8,C11,C15
C5 0.053 3 0 C1,C2,C3,C8,C11
C5 0.053 3 2 C2,C8,C11,C14,C15
C5 0.053 3 0 C2,C3,C4,C8,C9
C5 0.053 3 0 C2,C4,C7,C8,C11
C5 0.053 3 1 C2,C4,C8,C11,C15
C5 0.053 3 1 C2,C4,C8,C9,C11
C5 0.053 3 1 C2,C7,C8,C11,C15
C5 0.053 3 1 C5,C6,C12,C13,C14
C5 0.053 3 2 C5,C11,C12,C14,C15
C5 0.053 3 1 C5,C6,C10,C13,C14
C5 0.053 3 1 C5,C6,C10,C12,C14
C5 0.053 3 1 C5,C6,C10,C12,C13
C5 0.053 3 2 C5,C10,C12,C13,C14
C5 0.053 3 2 C5,C10,C12,C14,C15
C5 0.053 3 2 C5,C12,C13,C14,C15
C5 0.053 3 2 C6,C11,C13,C14,C15
C5 0.053 3 2 C6,C10,C12,C13,C14
C5 0.053 3 2 C6,C10,C13,C14,C15
C5 0.053 3 2 C6,C12,C13,C14,C15
C5 0.053 3 2 C7,C11,C12,C14,C15
C5 0.053 3 2 C7,C11,C13,C14,C15
C5 0.053 3 2 C7,C8,C11,C14,C15


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