Echinoderms Metabolites: Structure, Functions and Biomedical Perspectives II

The book largely reflect the structural diversity of echinoderm metabolites including triterpene glycosides and fucosylated chondroitin sulfates, as well as branched fatty acids, di- and triacylglycerols and other lipid classes from the sea cucumbers, polyhydroxysteroids from starfish and different...

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Bibliographic Details
Other Authors: Kalinin, Vladimir I. (Editor), Silchenko, Alexanra S. (Editor)
Format: Electronic Book Chapter
Language:English
Published: MDPI - Multidisciplinary Digital Publishing Institute 2022
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DOAB: description of the publication
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245 1 0 |a Echinoderms Metabolites: Structure, Functions and Biomedical Perspectives II 
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300 |a 1 electronic resource (192 p.) 
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520 |a The book largely reflect the structural diversity of echinoderm metabolites including triterpene glycosides and fucosylated chondroitin sulfates, as well as branched fatty acids, di- and triacylglycerols and other lipid classes from the sea cucumbers, polyhydroxysteroids from starfish and different classes of sphingolipids from sea cucumbers and starfish. Finally, the MS-based metabolomic approach, which is very helpful for the estimation of such diversity, is discussed. The materials from the Special Issue also illustrate the biomedical potential of the presented metabolites as cytotoxins and anticoagulants. The in silico approach broadens the possibilities to investigate the mechanisms of the action of membranolytic compounds. 
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650 7 |a Research & information: general  |2 bicssc 
650 7 |a Chemistry  |2 bicssc 
653 |a diacylglycerol ether 
653 |a 1-O-alkylglyceryl ether 
653 |a nutraceutical oils 
653 |a bêche-de-mer 
653 |a sea cucumber 
653 |a Bohadschia argus 
653 |a Holothuria (Theelothuria) spinifera 
653 |a fucosylated chondroitinsulfates 
653 |a fucan sulfates 
653 |a anticoagulant activity 
653 |a disulfated steroids 
653 |a NMR spectra 
653 |a starfish 
653 |a Pteraster marsippus 
653 |a cytotoxic activity 
653 |a 3D culture 
653 |a Psolus chitonoides 
653 |a triterpene glycosides 
653 |a chitonoidosides 
653 |a   triterpene glycosides 
653 |a membranolytic action 
653 |a hemolytic 
653 |a molecular dynamic simulation 
653 |a Thyonidium kurilensis 
653 |a kurilosides 
653 |a polyhydroxysteroids 
653 |a steroid glycosides 
653 |a lipids 
653 |a mass spectrometry 
653 |a metabolomics 
653 |a metabolomic profiling 
653 |a sphingolipids 
653 |a ceramides 
653 |a cerebrosides 
653 |a gangliosides 
653 |a sialic acid 
653 |a Asteroidea 
653 |a Holothuroidea 
653 |a biological activity 
653 |a neuritogenic activity 
653 |a   
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