MassBank Record: BS001156



 3-Glu(1-3)Glu-28-Xyl(1-4)[Api(1-3)]Rha(1-2)Ara Zanhic acid (NMR); LC-ESI-QTOF; MS2; CE:70 eV; [M-H]- 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: BS001156
RECORD_TITLE: 3-Glu(1-3)Glu-28-Xyl(1-4)[Api(1-3)]Rha(1-2)Ara Zanhic acid (NMR); LC-ESI-QTOF; MS2; CE:70 eV; [M-H]-
DATE: 2017.12.01 (2014.12.12)
AUTHORS: , Plant Biology, The Noble Foundation, Ardmore, OK, US/Dennis Fine, Daniel Wherritt, and Lloyd Sumner
LICENSE: CC BY-NC-SA 4.0 International

CH$NAME: 3-Glu(1-3)Glu-28-Xyl(1-4)[Api(1-3)]Rha(1-2)Ara Zanhic acid (NMR) CH$COMPOUND_CLASS: Natural Product; N/A CH$FORMULA: C63H100O33 CH$EXACT_MASS: 1384.6147 CH$SMILES: [C@H]1([C@@H]([C@@](C(=O)O)(C2[C@](C1)(C3[C@@](CC2)([C@]4(C(=CC3)[C@]5([C@@]([C@@H](C4)O)(CCC(C5)(C)C)C(O[C@H]6[C@@H]([C@H]([C@H](CO6)O)O)O[C@H]7[C@@H]([C@@H]([C@H]([C@@H](O7)C)O[C@H]8[C@@H]([C@H]([C@@H](CO8)O)O)O)O[C@@H]9OC[C@]([C@H]9O)(O)CO)O)=O)[H])C)C)C)C)O[C@@H]%10O[C@@H]([C@H]([C@@H]([C@H]%10O)O[C@@H]%11O[C@@H]([C@H]([C@@H]([C@H]%11O)O)O)CO)O)CO)O CH$IUPAC: InChI=1S/C63H100O33/c1-23-43(91-49-39(76)34(71)27(68)19-85-49)45(93-54-47(80)62(84,21-66)22-87-54)42(79)51(88-23)94-46-35(72)28(69)20-86-53(46)96-56(83)63-13-12-57(2,3)14-25(63)24-8-9-31-58(4)15-26(67)48(61(7,55(81)82)32(58)10-11-59(31,5)60(24,6)16-33(63)70)95-52-41(78)44(37(74)30(18-65)90-52)92-50-40(77)38(75)36(73)29(17-64)89-50/h8,23,25-54,64-80,84H,9-22H2,1-7H3,(H,81,82)/t23-,25-,26-,27+,28-,29+,30+,31?,32?,33+,34-,35-,36+,37+,38-,39+,40+,41+,42+,43-,44-,45-,46+,47-,48-,49-,50-,51-,52-,53-,54-,58+,59+,60+,61-,62+,63+/m0/s1 CH$LINK: INCHIKEY VCIIUHJUYQIBSQ-LOCYOFRUSA-N
AC$INSTRUMENT: Bruker impact HD AC$INSTRUMENT_TYPE: LC-ESI-QTOF AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE AC$MASS_SPECTROMETRY: COLLISION_ENERGY 70 eV AC$MASS_SPECTROMETRY: IONIZATION ESI AC$MASS_SPECTROMETRY: PEAK_WIDTH 0.013 AC$MASS_SPECTROMETRY: MASS_RANGE_M/Z 100-1500 AC$CHROMATOGRAPHY: COLUMN_NAME Waters Acquity BEH C18 1.7um x 2.1 x 150 mm AC$CHROMATOGRAPHY: FLOW_GRADIENT 95/5 at 0 min, 20/80 at 35 min; 5/95 at 35 min, 5/95 at 38 min; 95/5 at 38.1 min, 95/5 at 45 min AC$CHROMATOGRAPHY: FLOW_RATE FLOW_RATE 560 uL / min AC$CHROMATOGRAPHY: SOLVENT A water with 0.05% formic acid AC$CHROMATOGRAPHY: SOLVENT B acetonitrile with 0.05 % formic acid AC$CHROMATOGRAPHY: RETENTION_TIME 688.8 sec
MS$FOCUSED_ION: PRECURSOR_M/Z 1383.597 MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]- MS$DATA_PROCESSING: WHOLE convert from Bruker Library Editor (https://github.com/MassBank/MassBank2NIST)
PK$SPLASH: splash10-001i-0009200000-2ca675992aae28d377ff PK$NUM_PEAK: 10 PK$PEAK: m/z int. rel.int. 113.0240 84 84 337.1154 43 43 393.3087 18 18 455.3170 348 348 456.3173 96 96 469.1593 97 97 1383.6072 999 999 1384.6101 556 556 1385.6072 268 268 1386.6124 33 33 //

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