ACCESSION: MSBNK-RIKEN_ReSpect-PT211640
RECORD_TITLE: AMP 3'-phosphate, [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] dihydrogen phosphate, 3'-Adenylic acid, Synadenylic acid, 3'-Adenosine monophosphate, 3'-AMP, Adenosine 3'-monophosphate From Yeast; LC-ESI-QTOF; MS2
DATE: 2008.07.29
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$NAME: AMP 3'-phosphate
CH$NAME: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] dihydrogen phosphate
CH$NAME: 3'-Adenylic acid
CH$NAME: Synadenylic acid
CH$NAME: 3'-Adenosine monophosphate
CH$NAME: 3'-AMP
CH$NAME: Adenosine 3'-monophosphate From Yeast
CH$COMPOUND_CLASS: CLASS1 Other CLASS2 Nucleotide CLASS3 Adenosine phosphate
CH$FORMULA: C₁₀H₁₄N₅O₇P
CH$EXACT_MASS: 347.226
CH$SMILES: C1=NC2=C(C(=N1)N)N=CN2C3C(C(C(O3)CO)OP(=O)(O)O)O
CH$IUPAC: InChI=1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(17)7(4(1-16)21-10)22-23(18,19)20/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)
CH$LINK: CAS 84-21-9
CH$LINK: INCHIKEY LNQVTSROQXJCDD-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 NEGATIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: COLLISION_ENERGY Ramp 5-45 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 346.05528

PK$SPLASH: splash10-01u1-9463000000-deedf4a3a159267bf008
PK$NUM_PEAK: 5
PK$PEAK: m/z int. rel.int.
  78.9602 1514.0 999
  96.9704 392.5 259
  134.0473 866.0 571
  211.0013 1447.0 955
  346.0553 743.2 490
//