ACCESSION: MSBNK-RIKEN_ReSpect-PT100513
RECORD_TITLE: (2S)-2-amino-3-(3H-imidazol-4-yl)propanoic acid, L-Histidine, Glyoxaline-5-alanine, L-alpha-Amino-beta-imidazolepropionic Acid, (S)-2-Amino-3-(4-imidazolyl)propionic acid, L-His; LC-ESI-QTOF; MS2
DATE: 2008.07.24
AUTHORS: Matsuda F, Suzuki M, Sawada Y, Plant Science Center, RIKEN.
LICENSE: CC BY-NC
COPYRIGHT: Copyright(C) 2009 Plant Science Center, RIKEN
COMMENT: Build 1 2009/06/24
COMMENT: Acquisition and generation of the data is financially supported in part by CREST/JST.

CH$NAME: (2S)-2-amino-3-(3H-imidazol-4-yl)propanoic acid
CH$NAME: L-Histidine
CH$NAME: Glyoxaline-5-alanine
CH$NAME: L-alpha-Amino-beta-imidazolepropionic Acid
CH$NAME: (S)-2-Amino-3-(4-imidazolyl)propionic acid
CH$NAME: L-His
CH$COMPOUND_CLASS: CLASS1 Amino acid CLASS2 Histidine
CH$FORMULA: C₆H₉N₃O₂
CH$EXACT_MASS: 155.157
CH$SMILES: C1=C(NC=N1)CC(C(=O)O)N
CH$IUPAC: InChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)
CH$LINK: CAS 71-00-1
CH$LINK: INCHIKEY HNDVDQJCIGZPNO-UHFFFAOYSA-N

AC$INSTRUMENT: Q-Tof Premier, Waters
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 30 V
AC$MASS_SPECTROMETRY: CAPILLARY_VOLTAGE 3.0 kV
AC$CHROMATOGRAPHY: SOLVENT CH3CN/H2O

MS$FOCUSED_ION: ION_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_M/Z 156.07727

PK$SPLASH: splash10-0a4i-0900000000-23a17624cb20e8b396c8
PK$NUM_PEAK: 3
PK$PEAK: m/z int. rel.int.
  83.0618 2.097 129
  110.0706 4.908 301
  156.0772 16.3 999
//