scholarly journals Enhanced Glycosylation Detection and Characterization of a Human IgG1 Reference Material by using 2D‐LC MS/MS Fractionation and High Resolution Mass Spectral Library

2017 ◽  
Vol 31 (S1) ◽  
Author(s):  
Qian Dong ◽  
Xinjian Yan ◽  
Yuxue Liang ◽  
Stephen E. Stein

2019 ◽  
Vol 218 ◽  
pp. 29-51 ◽  
Author(s):  
Ryan P. Rodgers ◽  
Mmilili M. Mapolelo ◽  
Winston K. Robbins ◽  
Martha L. Chacón-Patiño ◽  
Jonathan C. Putman ◽  
...  

Here, we describe three separations that can help overcome selective ionization in the analysis of petroleum samples.



2015 ◽  
Vol 10 (9) ◽  
pp. 1934578X1501000 ◽  
Author(s):  
Venkata Sai Prakash Chaturvedula ◽  
Srinivasa Rao Meneni

A systematic phytochemical study of the commercial extract of Luo Han Guo ( Siraitia grosvenorii) resulted in the isolation of an additional minor new cucurbitane glycoside, mogroside V A1 (1). The structure of the new compound was characterized on the basis of 1D (1H and 13C NMR) and 2D (COSY, HMQC, HMBC and NOESY) NMR and high resolution mass spectral (HRMS) data, as well as hydrolysis studies.



Author(s):  
Fatima Saad ◽  
Boumedienne Bounaceur ◽  
Mortada Daaou ◽  
Juan Ramón Avilés-Moreno ◽  
Bruno Martínez-Haya


The Analyst ◽  
2021 ◽  
Author(s):  
Harald Schoeny ◽  
Evelyn Rampler ◽  
Yasin El Abiead ◽  
Felina Hildebrand ◽  
Olivia Zach ◽  
...  

We propose a fully automated novel workflow for lipidomics based on flow injection- followed by liquid chromatography high resolution mass spectrometry (FI/LC-HRMS). The workflow combined in-depth characterization of the lipidome...





1973 ◽  
Vol 135 (1) ◽  
pp. 133-143 ◽  
Author(s):  
Hans J. Förster ◽  
Klaus Biemann ◽  
W. Geoffrey Haigh ◽  
Neil H. Tattrie ◽  
J. Ross Colvin

A novel C35 terpene and its monounsaturated analogue were isolated from cultures of Acetobacter xylinum, together with traces of their C36 homologues. These substances were found to be hopane derivatives substituted by a five-carbon chain bearing four vicinal hydroxyl groups. For the parent hydrocarbon the term bacteriohopane is proposed. The elucidation of the structures utilized high-resolution mass spectrometry of the terpenes, degradation to C32 hydrocarbons and detailed mass-spectrometric comparison of these with C32 hydrocarbons synthesized from known pentacyclic triterpenes. High-resolution mass-spectral data of the terpenes are presented. N.m.r. data are in agreement with the proposed structures, which are further supported by the isolation from the same organism of 22-hydroxyhopane and derivative hopene(s).



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