Parotid saliva 1 H‐NMR analysis for colon cancer metabolomics: A case report

2021 ◽  
Author(s):  
Angela Rovera ◽  
Mark Hector ◽  
Paul Anderson

2006 ◽  
Vol 71 (10) ◽  
pp. 1470-1483 ◽  
Author(s):  
David Šaman ◽  
Pavel Kratina ◽  
Jitka Moravcová ◽  
Martina Wimmerová ◽  
Zdeněk Wimmer

Glucosylation of the cis- and trans-isomers of 2-(4-methoxybenzyl)cyclohexan-1-ol (1a/1b, 2a/2b, 1a or 2a) was performed to prepare the corresponding alkyl β-D-glucopyranosides, mainly to get analytical data of pure enantiomers of the glucosides (3a-6b), required for subsequent investigations of related compounds with biological activity. One of the employed modifications of the Koenigs-Knorr synthesis resulted in achieving 85-95% yields of pure β-anomers 3a/3b, 4a/4b, 3a or 4a of protected intermediates, with several promoters and toluene as solvent, yielding finally the deprotected products 5a/5b, 6a/6b, 5a or 6a as pure β-anomers. To obtain enantiomerically pure β-anomers of the target structure (3a, 4a, 5a and 6a) for unambiguous structure assignment, an enzymic reduction of 2-(4-methoxybenzyl)cyclohexan-1-one by Saccharomyces cerevisiae whole cells was performed to get (1S,2S)- and (1S,2R)-enantiomers (1a and 2a) of 2-(4-methoxybenzyl)cyclohexan-1-ol. The opposite enantiomers of alkyl β-D-glucopyranosides (5b and 6b) were obtained by separation of the diastereoisomeric mixtures 5a/5b and 6a/6b by chiral HPLC. All stereoisomers of the products (3a-6b) were subjected to a detailed 1H NMR and 13C NMR analysis.



2020 ◽  
Vol 92 (5-6) ◽  
pp. 182-185
Author(s):  
Roi Abramov ◽  
Subhi Mansour ◽  
Kenan Hallon ◽  
Bishara Bishara ◽  
Safi Khuri


2012 ◽  
Vol 506 ◽  
pp. 158-161 ◽  
Author(s):  
A. Jaidee ◽  
Pornchai Rachtanapun ◽  
S. Luangkamin

N,O-Carboxymethyl chitosans were synthesized by the reaction between shrimp, crab and squid chitosans with monochloroacetic acid under basic conditions at 50°C. The mole ratio of reactants was obtained from various reaction conditions of shrimp chitosan polymer and oligomer types. The mole ratio 1:12:6 of chitosan:sodium hydroxide:monochloroacetic acid was used for preparing carboxymethyl of chitosan polymer types while carboxymethyl of chitosan oligomer types were used the mole ratio 1:6:3 of chitosan:sodium hydroxide:monochloroacetic acid. The chemical structure was analyzed by fourier transformed infrared spectroscopy (FT-IR) and proton nuclear magnatic resonance spectroscopy (1H-NMR). The FT-IR was used for confirm the insertion of carboxymethyl group on chitosan molecules. The 1H-NMR was used for determining the degree of substitution (DS) of carboxymethylation at hydroxyl and amino sites of chitosans. Carboxymethyl chitosan samples had the total DS of carboxymethylation ranging from 1.0-2.2. The highest of DS of carboxymethylation was from shrimp chitosan oligomer type.





2016 ◽  
Vol 14 (1) ◽  
Author(s):  
Keiichi Arakawa ◽  
Soichiro Ishihara ◽  
Kazushige Kawai ◽  
Junichi Shibata ◽  
Kensuke Otani ◽  
...  


2013 ◽  
Vol 7 (3) ◽  
pp. 797-798
Author(s):  
DENIZ ARSLAN ◽  
FATMA AVCI ◽  
ALPARSLAN MERDIN ◽  
SEYDA GUNDUZ ◽  
HASAN SENOL COSKUN


Author(s):  
A. Haddad ◽  
D. Bel Haj Yahia ◽  
Y. Chaker ◽  
H. Maghrebi ◽  
A. Daghfous ◽  
...  




2014 ◽  
Vol 8 (6) ◽  
pp. 2672-2674 ◽  
Author(s):  
DO HYOUNG LIM ◽  
SOON IL LEE ◽  
KEON WOO PARK


2018 ◽  
Vol 5 (1-2) ◽  
pp. 59-62
Author(s):  
Tsung-Jung Lin ◽  
Ting-An Chang ◽  
Chin-Tsung Ting ◽  
Chih-Lin Lin ◽  
Kuan-Yang Chen
Keyword(s):  


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