Name:
Adduct:
Polarity:
Z:
m/z:
±:
CCS: Å2
±: %
SMI:
Type:

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1
May, J. C. et al. Conformational Ordering of Biomolecules in the Gas Phase: Nitrogen Collision Cross Sections Measured on a Prototype High Resolution Drift Tube Ion Mobility-Mass Spectrometer. Anal. Chem. 86, 2107–2116 (2014).


2
Paglia, G. et al. Ion Mobility Derived Collision Cross Sections to Support Metabolomics Applications. Anal. Chem. 86, 3985–3993 (2014).


3
Groessl, M., Graf, S. & Knochenmuss, R. High resolution ion mobility-mass spectrometry for separation and identification of isomeric lipids. Analyst 140, 6904–6911 (2015).


4
Zhou, Z., Shen, X., Tu, J. & Zhu, Z.-J. Large-Scale Prediction of Collision Cross-Section Values for Metabolites in Ion Mobility-Mass Spectrometry. Anal. Chem. 88, 11084–11091 (2016).


5
Hines, K. M., Herron, J. & Xu, L. Assessment of altered lipid homeostasis by HILIC-ion mobility-mass spectrometry-based lipidomics. The Journal of Lipid Research 58, 809–819 (2017).


6
Bijlsma, L. et al. Prediction of Collision Cross-Section Values for Small Molecules: Application to Pesticide Residue Analysis. Anal. Chem. 89, 6583–6589 (2017).


7
Hines, K. M., Ross, D. H., Davidson, K. L., Bush, M. F. & Xu, L. Large-Scale Structural Characterization of Drug and Drug-Like Compounds by High-Throughput Ion Mobility-Mass Spectrometry. Anal. Chem. 89, 9023–9030 (2017).


8
Stow, S. M. et al. An Interlaboratory Evaluation of Drift Tube Ion Mobility–Mass Spectrometry Collision Cross Section Measurements. Anal. Chem. 89, 9048–9055 (2017).


9
Zhou, Z., Tu, J., Xiong, X., Shen, X. & Zhu, Z.-J. LipidCCS: Prediction of Collision Cross-Section Values for Lipids with High Precision To Support Ion Mobility–Mass Spectrometry-Based Lipidomics. Anal. Chem. 89, 9559–9566 (2017).


10
Zheng, X. et al. A structural examination and collision cross section database for over 500 metabolites and xenobiotics using drift tube ion mobility spectrometry. Chem. Sci. 8, 7724–7736 (2017).


11
Hines, K. M. et al. Characterization of the Mechanisms of Daptomycin Resistance among Gram-Positive Bacterial Pathogens by Multidimensional Lipidomics. mSphere 2, 99–16 (2017).


12
Lian, R. et al. Ion mobility derived collision cross section as an additional measure to support the rapid analysis of abused drugs and toxic compounds using electrospray ion mobility time-of-flight mass spectrometry. Anal. Methods 10, 749–756 (2018).


13
Mollerup, C. B., Mardal, M., Dalsgaard, P. W., Linnet, K. & Barron, L. P. Prediction of collision cross section and retention time for broad scope screening in gradient reversed-phase liquid chromatography-ion mobility-high resolution accurate mass spectrometry. Journal of Chromatography A 1542, 82–88 (2018).


14
Righetti, L. et al. Ion mobility-derived collision cross section database: Application to mycotoxin analysis. Analytica Chimica Acta 1014, 50–57 (2018).


15
Tejada-Casado, C. et al. Collision cross section (CCS) as a complementary parameter to characterize human and veterinary drugs. Analytica Chimica Acta 1043, 52–63 (2018).


16
Nichols, C. M. et al. Untargeted Molecular Discovery in Primary Metabolism: Collision Cross Section as a Molecular Descriptor in Ion Mobility-Mass Spectrometry. Anal. Chem. 90, 14484–14492 (2018).


17
Hines, K. M. & Xu, L. Lipidomic consequences of phospholipid synthesis defects in Escherichia coli revealed by HILIC-ion mobility-mass spectrometry. Chemistry and Physics of Lipids 219, 15–22 (2019).


18
Leaptrot, K. L., May, J. C., Dodds, J. N. & McLean, J. A. Ion mobility conformational lipid atlas for high confidence lipidomics. Nature Communications 1–9 (2019).


19
Blaženović, I. et al. Increasing Compound Identification Rates in Untargeted Lipidomics Research with Liquid Chromatography Drift Time–Ion Mobility Mass Spectrometry. Anal. Chem. 90, 10758–10764 (2018).


20
Vasilopoulou, C. G. et al. Trapped ion mobility spectrometry and PASEF enable in-depth lipidomics from minimal sample amounts. Nature Communications 1–11 (2020).


21
Tsugawa, H. et al. MS-DIAL 4: accelerating lipidomics using an MS/MS, CCS, and retention time atlas. bioRxiv 37, 513 (2020).


22
Poland, J. C. et al. Collision Cross Section Conformational Analyses of Bile Acids via Ion Mobility–Mass Spectrometry. Journal of the American Society for Mass Spectrometry 31, 1625–1631 (2020).


23
Dodds, J. et al. Rapid Characterization of Per- and Polyfluoroalkyl Substances (PFAS) by Ion Mobility Spectrometry−Mass Spectrometry (IMS-MS). Anal. Chem. 92, 4427-4435 (2020).


24
Celma, A. et al. Improving Target and Suspect Screening High-Resolution Mass Spectrometry Workflows in Environmental Analysis by Ion Mobility Separation. Environ. Sci. Technol. 54, 15120-15131 (2020)


25
Belova, L. et al. Ion Mobility-High-Resolution Mass Spectrometry (IM-HRMS) for the Analysis of Contaminants of Emerging Concern (CECs): Database Compilation and Application to Urine Samples. Anal. Chem. XXX, XXXX-XXXX (2021)


26
Ross, D. H., et al. High-Throughput Measurement and Machine Learning-Based Prediction of Collision Cross Sections for Drugs and Drug Metabolites. J Am Soc Mass Spectr 33, 1061–1072 (2022).


ID Name Adduct Structure m/z CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_16AF9F65CA PG(30:0) [M-H]- 693.4721 258.02 CCCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO)OC(=O)CCCCCCCCCCCCC lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_76EA9C71B3 PG(31:1) [M-H]- 705.4726 259.19 CCCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO)OC(=O)CCCCCCCC1CC1CCCC lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_801CA6F691 PG(32:2) [M-H]- 717.474 261.31 CCCCCC\C=C/CCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO)OC(=O)CCCCCCC\C=C/CCCCCC lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_52068A2499 PG(32:1) [M-H]- 719.4906 262.68 CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC\C=C/CCCCCC)CO[P](O)(=O)OCC(O)CO lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_C0893B960C PG(32:0) [M-H]- 721.4983 263.91 CCCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO)OC(=O)CCCCCCCCCCCCCCC lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_43B585310C PG(33:2) [M-H]- 731.4873 264.54 CCCCCC\C=C/CCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO)OC(=O)CCCCCCCC1CC1CCCCCC lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_6E22890DA6 PG(33:1) [M-H]- 733.5067 266.36 CCCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO)OC(=O)CCCCCCCC1CC1CCCCCC lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_CA1772A520 PG(34:2) [M-H]- 745.5033 267.97 CCCCCCCC\C=C/CCCCCCCC(=O)OC(COC(=O)CCCCCCC\C=C/CCCCCC)CO[P](O)(=O)OCC(O)CO lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_B6EAE09F54 PG(34:1) [M-H]- 747.5209 270.03 CCCCCCCCCCCCCCCC(=O)OCC(CO[P](O)(=O)OCC(O)CO)OC(=O)CCCCCCC\C=C/CCCCCCCC lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
CCSBASE_B669EAC754 PG(35:2) [M-H]- 759.5188 271.85 CCCCCCCCC1CC1CCCCCCCC(=O)OC(COC(=O)CCCCCCC\C=C/CCCCCC)CO[P](O)(=O)OCC(O)CO lipid 1 17 TW calibrated with phosphatidylcholines (ESI+) and phosphatidylethanolamines (ESI-), doubly charged cardiolipins calibrated with poly-DL-alanine
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