Identification of Oxidation Products of Squalene in Solution and in Latent Fingerprints by ESI-MS and LC/APCI-MS

2007 ◽  
Vol 79 (7) ◽  
pp. 2650-2657 ◽  
Author(s):  
Katrina A. Mountfort ◽  
Hugo Bronstein ◽  
Nia Archer ◽  
Sue M. Jickells
Molecules ◽  
2020 ◽  
Vol 25 (20) ◽  
pp. 4778
Author(s):  
Natalia P. Mishchenko ◽  
Elena A. Vasileva ◽  
Andrey V. Gerasimenko ◽  
Valeriya P. Grigorchuk ◽  
Pavel S. Dmitrenok ◽  
...  

Echinochrome A (Ech A, 1) is one of the main pigments of several sea urchin species and is registered in the Russian pharmacopeia as an active drug substance (Histochrome®), used in the fields of cardiology and ophthalmology. In this study, Ech A degradation products formed during oxidation by O2 in air-equilibrated aqueous solutions were identified, isolated, and structurally characterized. An HPLC method coupled with diode-array detection (DAD) and mass spectrometry (MS) was developed and validated to monitor the Ech A degradation process and identify the appearing compounds. Five primary oxidation products were detected and their structures were proposed on the basis of high-resolution electrospray ionization mass spectrometry (HR-ESI-MS) as 7-ethyl-2,2,3,3,5,7,8-heptahydroxy-2,3-dihydro-1,4-naphthoquinone (2), 6-ethyl-5,7,8-trihydroxy-1,2,3,4-tetrahydronaphthalene-1,2,3,4-tetraone (3), 2,3-epoxy-7-ethyl-2,3-dihydro-2,3,5,6,8-pentahydroxy-1,4-naphthoquinone (4), 2,3,4,5,7-pentahydroxy-6-ethylinden-1-one (5), and 2,2,4,5,7-pentahydroxy-6-ethylindane-1,3-dione (6). Three novel oxidation products were isolated, and NMR and HR-ESI-MS methods were used to establish their structures as 4-ethyl-3,5,6-trihydroxy-2-oxalobenzoic acid (7), 4-ethyl-2-formyl-3,5,6-trihydroxybenzoic acid (8), and 4-ethyl-2,3,5-trihydroxybenzoic acid (9). The known compound 3-ethyl-2,5-dihydroxy-1,4-benzoquinone (10) was isolated along with products 7–9. Compound 7 turned out to be unstable; its anhydro derivative 11 was obtained in two crystal forms, the structure of which was elucidated using X-ray crystallography as 7-ethyl-5,6-dihydroxy-2,3-dioxo-2,3-dihydrobenzofuran-4-carboxylic acid and named echinolactone. The chemical mechanism of Ech A oxidative degradation is proposed. The in silico toxicity of Ech A and its degradation products 2 and 7–10 were predicted using the ProTox-II webserver. The predicted median lethal dose (LD50) value for product 2 was 221 mg/kg, and, for products 7–10, it appeared to be much lower (≥2000 mg/kg). For Ech A, the predicted toxicity and mutagenicity differed from our experimental data.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Katelyn W. Ahern ◽  
Vlad Serbulea ◽  
Catherine L. Wingrove ◽  
Zachary T. Palas ◽  
Norbert Leitinger ◽  
...  

2019 ◽  
Vol 6 (17) ◽  
pp. 4511-4521 ◽  
Author(s):  
Isabella Chiarotto ◽  
Leonardo Mattiello ◽  
Fabiana Pandolfi ◽  
Daniele Rocco ◽  
Marta Feroci ◽  
...  

2011 ◽  
Vol 125 (1) ◽  
pp. 21-28 ◽  
Author(s):  
Ilona Di Maio ◽  
Sonia Esposto ◽  
Agnese Taticchi ◽  
Roberto Selvaggini ◽  
Gianluca Veneziani ◽  
...  

2021 ◽  
Vol 353 ◽  
pp. 129455
Author(s):  
Andrew J. Hambly ◽  
Jeroen S. van Duijneveldt ◽  
Paul J. Gates

Planta Medica ◽  
2011 ◽  
Vol 77 (12) ◽  
Author(s):  
A Karioti ◽  
J Kukic Markovic ◽  
S Petrovic ◽  
M Niketic ◽  
A Bilia

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