Automated Isotopic Profile Deconvolution for High Resolution Mass Spectrometric Data (APGC-QToF) from Biological Matrices

2019 ◽  
Vol 91 (24) ◽  
pp. 15509-15517 ◽  
Author(s):  
Sadjad Fakouri Baygi ◽  
Sujan Fernando ◽  
Philip K. Hopke ◽  
Thomas M. Holsen ◽  
Bernard S. Crimmins
2010 ◽  
Vol 5 (3) ◽  
pp. 1934578X1000500
Author(s):  
Seru Ganapaty ◽  
Desaraju Venkata Rao ◽  
Steve Thomas Pannakal

A new compound, (2 S)- p-hydroxyphenethyl 2-bromo-2-methyldodeconate (1) and 7,3′-dimethoxy-5,4′-dihydroxy flavone, together with lupeol and stigmasterol were isolated from the stem bark of Citharexylum fruticosum (Verbenaceae). The structures of the compounds were established on the basis of the interpretation of NMR (1H, 13C, COSY and HMBC) spectra, as well as low and high-resolution mass spectrometric data. In this paper, we report on the structure elucidation of 1.


2016 ◽  
Vol 15 (3) ◽  
pp. 851-867 ◽  
Author(s):  
Kai-Ting Fan ◽  
Aaron K. Rendahl ◽  
Wen-Ping Chen ◽  
Dana M. Freund ◽  
William M. Gray ◽  
...  

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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