Reprint

Echinoderms Metabolites: Structure, Functions and Biomedical Perspectives

Edited by
September 2021
196 pages
  • ISBN978-3-0365-1594-6 (Hardback)
  • ISBN978-3-0365-1593-9 (PDF)

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

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

The materials published in the Special Issue reflect the real diversity of echinoderm metabolites and cover most of their specific classes and biomedical potential as antioxidant, antiviral, anticancer, and even anticoagulant preparations. The metabolites include sea urchin naphtoquinoid pigments and their semi-synthetic derivatives, sea cucumber triterpene glycosides, esters of polyhydroxysteroids from starfish, sea urchins free sterols, and sea cucumber fucosylated chondroitin sulfates. This Special Issue, “Echinoderm Metabolites: Structure, Functions, and Biomedical Perspectives”, is a collection of articles about different scientific aspects concerning low molecular weight and biopolymer metabolites from echinoderms, including their isolation and chemical structures, biological activities, biosynthesis and evolution, biological functions, and obtaining of semi-synthetic derivatives of biologically active natural products. This Special Issue includes materials about sea urchin naphtoquinoid pigments and their semi-synthetic derivatives, sea cucumber triterpene glycosides, esters of polyhydroxysteroids from starfish, sea urchin free sterols, and sea cucumber fucosylated chondroitin sulfates.

Format
  • Hardback
License
© 2022 by the authors; CC BY-NC-ND license
Keywords
prostate cancer; thioglucoside conjugates; natural products; sea urchins; glucose uptake; polyhydroxysteroidal esters; NMR spectra; fatty acids; starfish; Ceramaster patagonicus; cytostatic activity; soft agar assay; wound healing assay; Colochirus quadrangularis; triterpene glycosides; quadrangularisosides; sea cucumber; cytotoxic activity; sea cucumber; Holothuria hilla; Paracaudina chilensis; fucosylated chondroitin sulfate; anticoagulant activity; echinochrome A; echinamine A; echinamine B; herpes simplex virus type 1; Vero cells; glycoprotein gD; molecular docking; Thyonidium kurilensis; triterpene glycosides; kurilosides; sea cucumber; cytotoxic activity; Thenea muricata; Aplysina sp.; Pseudoanthomastus agaricus; Montastraea cavernosa; Buccinum sp.; Pasiphaea tarda; Phormosoma placenta; Echinometra lucunter; sterols; gas chromatography; mass spectrometry; neuroblastoma Neuro-2a cells; 5,8-dihydroxy-1,4-naphthoquinone; O-glucoside; thiomethylglycoside; cytotoxic activity; QSAR; n/a