MassBank Record: BS001223



 3-Glc(1-2)Glc(1-2)Glc-28-Api(1-3)Xyl(1-4)[Api(1-3)]Rha(1-2)Ara Zanhic acid (NMR); LC-ESI-QTOF; MS2; CE:105 eV; [M-H]- 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: BS001223
RECORD_TITLE: 3-Glc(1-2)Glc(1-2)Glc-28-Api(1-3)Xyl(1-4)[Api(1-3)]Rha(1-2)Ara Zanhic acid (NMR); LC-ESI-QTOF; MS2; CE:105 eV; [M-H]-
DATE: 2017.12.01 (2015.01.15)
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$NAME: 3-Glc(1-2)Glc(1-2)Glc-28-Api(1-3)Xyl(1-4)[Api(1-3)]Rha(1-2)Ara Zanhic acid (NMR) CH$COMPOUND_CLASS: Natural Product; N/A CH$FORMULA: C74H118O42 CH$EXACT_MASS: 1678.7098 CH$SMILES: [C@H]1([C@@H]([C@@](C(=O)O)(C2[C@](C1)(C3[C@@](CC2)([C@]4(C(=CC3)[C@]5([C@@]([C@@H](C4)O)(CCC(C5)(C)C)C(O[C@H]6[C@@H]([C@H]([C@H](CO6)O)O)O[C@H]7[C@@H]([C@@H]([C@H]([C@@H](O7)C)O[C@H]8[C@@H]([C@H]([C@@H](CO8)O)O[C@@H]9OC[C@@]([C@H]9O)(CO)O)O)O[C@@H]%10OC[C@]([C@H]%10O)(O)CO)O)=O)[H])C)C)C)C)O[C@@H]%11O[C@@H]([C@H]([C@@H]([C@H]%11O[C@@H]%12O[C@@H]([C@H]([C@@H]([C@H]%12O[C@@H]%13O[C@@H]([C@H]([C@@H]([C@H]%13O)O)O)CO)O)O)CO)O)O)CO)O CH$IUPAC: InChI=1S/C74H118O42/c1-26-48(109-57-46(92)49(31(82)21-101-57)110-63-54(94)72(99,22-78)24-103-63)50(111-64-55(95)73(100,23-79)25-104-64)47(93)59(105-26)112-51-38(84)30(81)20-102-60(51)116-66(98)74-13-12-67(2,3)14-28(74)27-8-9-35-68(4)15-29(80)56(71(7,65(96)97)36(68)10-11-69(35,5)70(27,6)16-37(74)83)115-62-53(44(90)41(87)34(19-77)108-62)114-61-52(43(89)40(86)33(18-76)107-61)113-58-45(91)42(88)39(85)32(17-75)106-58/h8,26,28-64,75-95,99-100H,9-25H2,1-7H3,(H,96,97)/t26-,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-,55-,56-,57-,58-,59-,60-,61-,62-,63-,64-,68+,69+,70+,71-,72+,73+,74+/m0/s1 CH$LINK: INCHIKEY VNHLGJLOJBJFGV-OMOYKTNYSA-N
AC$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 105 eV AC$MASS_SPECTROMETRY: IONIZATION ESI AC$MASS_SPECTROMETRY: PEAK_WIDTH 0.018 AC$MASS_SPECTROMETRY: MASS_RANGE_M/Z 100-2250 AC$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$CHROMATOGRAPHY: RETENTION_TIME 660.6 sec
MS$FOCUSED_ION: PRECURSOR_M/Z 1677.698 MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]- MS$DATA_PROCESSING: WHOLE convert from Bruker Library Editor (https://github.com/MassBank/MassBank2NIST)
PK$SPLASH: splash10-0fb9-0001209000-ace0ae03da1c3a8eae09 PK$NUM_PEAK: 27 PK$PEAK: m/z int. rel.int. 113.0254 11 11 149.0468 14 14 221.0652 67 67 263.0771 97 97 337.1156 91 91 383.1165 334 334 384.1251 22 22 409.1407 31 31 455.3151 228 228 456.3136 48 48 469.1534 434 434 470.1552 63 63 541.1778 215 215 542.1835 23 23 601.1974 999 999 602.2004 236 236 603.2026 18 18 673.2183 141 141 674.2230 47 47 1003.4775 123 123 1004.4818 39 39 1129.5402 97 97 1677.6920 918 918 1678.5742 19 19 1678.6935 716 716 1679.7064 333 333 1680.6869 86 86 //

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