MassBank Record: UF415353



 Cholic acid; LC-ESI-ITFT; MS2; CE: 35; R=15000; [M-H]- 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: UF415353
RECORD_TITLE: Cholic acid; LC-ESI-ITFT; MS2; CE: 35; R=15000; [M-H]-
DATE: 2017.01.05
AUTHORS: Schulze T, Krauss M, Department of Effect-Directed Analysis, Helmholtz Centre for Environmental Research - UFZ GmbH, Leipzig, Germany
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2017
PUBLICATION: 
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 4153

CH$NAME: Cholic acid CH$NAME: (4R)-4-[(3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-Trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid CH$COMPOUND_CLASS: N/A; Environmental Standard CH$FORMULA: C24H40O5 CH$EXACT_MASS: 408.2876 CH$SMILES: C[C@H](CCC(O)=O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@]12C CH$IUPAC: InChI=1S/C24H40O5/c1-13(4-7-21(28)29)16-5-6-17-22-18(12-20(27)24(16,17)3)23(2)9-8-15(25)10-14(23)11-19(22)26/h13-20,22,25-27H,4-12H2,1-3H3,(H,28,29)/t13-,14+,15-,16-,17+,18+,19-,20+,22+,23+,24-/m1/s1 CH$LINK: CAS 81-25-4 CH$LINK: CHEBI 16359 CH$LINK: KEGG C00695 CH$LINK: LIPIDMAPS LMST04010001 CH$LINK: PUBCHEM CID:221493 CH$LINK: INCHIKEY BHQCQFFYRZLCQQ-OELDTZBJSA-N CH$LINK: CHEMSPIDER 192176
AC$INSTRUMENT: LTQ Orbitrap XL Thermo Scientific AC$INSTRUMENT_TYPE: LC-ESI-ITFT AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: IONIZATION ESI AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID AC$MASS_SPECTROMETRY: COLLISION_ENERGY 35 (nominal) AC$MASS_SPECTROMETRY: RESOLUTION 15000 AC$CHROMATOGRAPHY: COLUMN_NAME Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0 min, 80/20 at 3.2 min, 5/95 at 17.8 min, 5/95 at 37.8 min, 90/10 at 37.9 min, 90/10 at 47 min AC$CHROMATOGRAPHY: FLOW_RATE 200 uL/min AC$CHROMATOGRAPHY: RETENTION_TIME 26.581 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 453.2859 MS$FOCUSED_ION: PRECURSOR_M/Z 407.2803 MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]- MS$DATA_PROCESSING: RECALIBRATE loess on assigned fragments and MS1 MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included MS$DATA_PROCESSING: WHOLE RMassBank 2.2.1
PK$SPLASH: splash10-005z000000-285d3d0d87f5471b419a PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 188.0848 C12H12O2- 1 188.0843 2.74 193.1602 C13H21O- 1 193.1598 2.15 205.1598 C14H21O- 1 205.1598 0.12 233.1908 C16H25O- 1 233.1911 -1.09 249.1861 C16H25O2- 1 249.186 0.53 251.2016 C16H27O2- 1 251.2017 -0.13 289.2173 C19H29O2- 1 289.2173 -0.17 315.2686 C22H35O- 1 315.2693 -2.46 323.2382 C23H31O- 1 323.238 0.5 325.2535 C23H33O- 1 325.2537 -0.53 327.2692 C23H35O- 1 327.2693 -0.51 333.279 C22H37O2- 1 333.2799 -2.73 335.2383 C24H31O- 1 335.238 0.81 341.2485 C23H33O2- 1 341.2486 -0.23 343.2641 C23H35O2- 1 343.2643 -0.4 345.2796 C23H37O2- 1 345.2799 -1.01 351.2325 C24H31O2- 1 351.233 -1.23 353.2484 C24H33O2- 1 353.2486 -0.53 361.2756 C23H37O3- 1 361.2748 2.15 363.2903 C23H39O3- 1 363.2905 -0.46 369.244 C24H33O3- 1 369.2435 1.21 371.2589 C24H35O3- 1 371.2592 -0.68 387.2539 C24H35O4- 1 387.2541 -0.52 389.2697 C24H37O4- 1 389.2697 -0.12 PK$NUM_PEAK: 24 PK$PEAK: m/z int. rel.int. 188.0848 5184.7 8 193.1602 8177.5 12 205.1598 6614.6 10 233.1908 10239.2 16 249.1861 7492 11 251.2016 68447.2 107 289.2173 148664 232 315.2686 4803.4 7 323.2382 14648.5 22 325.2535 90878.1 142 327.2692 111589.5 174 333.279 3886.8 6 335.2383 7862.8 12 341.2485 37201.5 58 343.2641 637907.6 999 345.2796 463682.3 726 351.2325 12909.3 20 353.2484 138972.4 217 361.2756 7554.6 11 363.2903 35293.9 55 369.244 4940.1 7 371.2589 67351 105 387.2539 9446.7 14 389.2697 35192.4 55 //