ACCESSION: MSBNK-Athens_Univ-AU263505
RECORD_TITLE: Spinosyn A; LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
DATE: 2019.05.30
AUTHORS: Nikiforos Alygizakis, Katerina Galani, Nikolaos Thomaidis, University of Athens
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2019 Department of Chemistry, University of Athens
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 2635

CH$NAME: Spinosyn A
CH$NAME: Spinosad factor A
CH$NAME: (1S,2R,5S,7R,9R,10S,14R,15S,19S)-15-[(2R,5S,6R)-5-(dimethylamino)-6-methyloxan-2-yl]oxy-19-ethyl-14-methyl-7-[(2R,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyloxan-2-yl]oxy-20-oxatetracyclo[10.10.0.02,10.05,9]docosa-3,11-diene-13,21-dione
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C₄₁H₆₅NO₁₀
CH$EXACT_MASS: 731.4608473
CH$SMILES: [H][C@]1(C[C@@]2([H])C=C[C@@]3([H])[C@]4([H])CC(=O)O[C@@]([H])(CC)CCC[C@]([H])(O[C@@]5([H])CC[C@]([H])(N(C)C)[C@@]([H])(C)O5)[C@@]([H])(C)C(=O)C4=C[C@@]3([H])[C@]2([H])C1)O[C@]1([H])O[C@@]([H])(C)[C@]([H])(OC)[C@@]([H])(OC)[C@@]1([H])OC
CH$IUPAC: InChI=1S/C41H65NO10/c1-10-26-12-11-13-34(52-36-17-16-33(42(5)6)23(3)48-36)22(2)37(44)32-20-30-28(31(32)21-35(43)50-26)15-14-25-18-27(19-29(25)30)51-41-40(47-9)39(46-8)38(45-7)24(4)49-41/h14-15,20,22-31,33-34,36,38-41H,10-13,16-19,21H2,1-9H3/t22-,23-,24+,25-,26+,27-,28-,29-,30-,31+,33+,34+,36+,38+,39-,40-,41+/m1/s1
CH$LINK: CAS 131929-60-7
CH$LINK: CHEBI 9230
CH$LINK: KEGG C11054
CH$LINK: PUBCHEM CID:443059
CH$LINK: INCHIKEY SRJQTHAZUNRMPR-UYQKXTDMSA-N
CH$LINK: CHEMSPIDER 391358
CH$LINK: COMPTOX DTXSID8037598

AC$INSTRUMENT: Bruker maXis Impact
AC$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: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 50 eV
AC$MASS_SPECTROMETRY: RESOLUTION 35000
AC$CHROMATOGRAPHY: COLUMN_NAME Acclaim RSLC C18 2.2um, 2.1x100mm, Thermo
AC$CHROMATOGRAPHY: FLOW_GRADIENT 99/1 at 0-1 min, 61/39 at 3 min, 0.1/99.9 at 14-16 min, 99/1 at 16.1-20 min
AC$CHROMATOGRAPHY: FLOW_RATE 200 uL/min at 0-3 min, 400 uL/min at 14 min, 480 uL/min at 16-19 min, 200 uL/min at 19.1-20 min
AC$CHROMATOGRAPHY: RETENTION_TIME 11.178 min
AC$CHROMATOGRAPHY: SOLVENT A 90:10 water:methanol with 0.01% formic acid and 5mM ammonium formate
AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.01% formic acid and 5mM ammonium formate

MS$FOCUSED_ION: BASE_PEAK 732.4671
MS$FOCUSED_ION: PRECURSOR_M/Z 732.4681
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: RECALIBRATE identity on assigned fragments and MS1
MS$DATA_PROCESSING: WHOLE RMassBank 2.10.1

PK$SPLASH: splash10-0006-0900000000-b3d348e190f926ea85d3
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  124.111 C8H14N+ 2 124.1121 -8.55
  125.0588 C7H9O2+ 1 125.0597 -7.41
  129.0898 C7H13O2+ 1 129.091 -9.04
  142.1217 C5H18O4+ 2 142.12 12.32
  143.1248 C4[13]CH18O4+ 1 143.1239 6.53
  145.0846 C7H13O3+ 1 145.0859 -9.32
  155.0835 C12H11+ 1 155.0855 -13.21
  157.0846 C8H13O3+ 1 157.0859 -8.34
  160.1319 C8H18NO2+ 2 160.1332 -8.27
  189.111 C9H17O4+ 2 189.1121 -6.16
  190.1142 C8[13]CH17O4+ 1 190.116 -9.75
  199.074 C13H11O2+ 1 199.0754 -6.64
  201.0896 C13H13O2+ 1 201.091 -6.88
  215.1061 C14H15O2+ 1 215.1067 -2.51
  225.0907 C15H13O2+ 1 225.091 -1.35
PK$NUM_PEAK: 15
PK$PEAK: m/z int. rel.int.
  124.111 5540 5
  125.0588 12956 12
  129.0898 11652 11
  142.1217 1037180 999
  143.1248 78888 75
  145.0846 23156 22
  155.0835 5256 5
  157.0846 40980 39
  160.1319 29188 28
  189.111 75556 72
  190.1142 8572 8
  199.074 6932 6
  201.0896 6460 6
  215.1061 6496 6
  225.0907 9900 9
//