Reprint

Echinoderms Metabolites: Structure, Functions and Biomedical Perspectives II

Edited by
September 2022
192 pages
  • ISBN978-3-0365-5129-6 (Hardback)
  • ISBN978-3-0365-5130-2 (PDF)

This book is a reprint of the Special Issue Echinoderms Metabolites: Structure, Functions and Biomedical Perspectives II that was published in

Biology & Life Sciences
Chemistry & Materials Science
Medicine & Pharmacology
Summary

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.

Format
  • Hardback
License
© 2022 by the authors; CC BY-NC-ND license
Keywords
Thyonidium kurilensis; triterpene glycosides; kurilosides; sea cucumber; cytotoxic activity; sphingolipids; ceramides; cerebrosides; gangliosides; sialic acid; Asteroidea; Holothuroidea; biological activity; neuritogenic activity; triterpene glycosides; sea cucumber; membranolytic action; hemolytic; cytotoxic activity; molecular dynamic simulation; Psolus chitonoides; triterpene glycosides; chitonoidosides; sea cucumber; cytotoxic activity; disulfated steroids; NMR spectra; starfish; Pteraster marsippus; cytotoxic activity; 3D culture; starfish; sea cucumber; polyhydroxysteroids; triterpene glycosides; steroid glycosides; lipids; mass spectrometry; metabolomics; metabolomic profiling; sea cucumber; Bohadschia argus; Holothuria (Theelothuria) spinifera; fucosylated chondroitin sulfates; fucan sulfates; anticoagulant activity; diacylglycerol ether; 1-O-alkylglyceryl ether; nutraceutical oils; bêche-de-mer; n/a