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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| HerausgeberIn: | |
|---|---|
| Sonstige: | |
| Year of Publication: | 2022 |
| Language: | English |
| Physical Description: | 1 electronic resource (192 p.) |
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| 041 | 0 | |a eng | |
| 100 | 1 | |a Kalinin, Vladimir I. |4 edt | |
| 245 | 1 | 0 | |a Echinoderms Metabolites: Structure, Functions and Biomedical Perspectives II |
| 246 | |a Echinoderms Metabolites | ||
| 260 | |b MDPI - Multidisciplinary Digital Publishing Institute |c 2022 | ||
| 300 | |a 1 electronic resource (192 p.) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 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. | ||
| 546 | |a English | ||
| 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 | ||
| 776 | |z 3-0365-5129-8 | ||
| 700 | 1 | |a Silchenko, Alexanra S. |4 edt | |
| 700 | 1 | |a Kalinin, Vladimir I. |4 oth | |
| 700 | 1 | |a Silchenko, Alexanra S. |4 oth | |
| 906 | |a BOOK | ||
| ADM | |b 2023-12-15 05:39:43 Europe/Vienna |f system |c marc21 |a 2022-11-05 21:33:14 Europe/Vienna |g false | ||
| AVE | |i DOAB Directory of Open Access Books |P DOAB Directory of Open Access Books |x https://eu02.alma.exlibrisgroup.com/view/uresolver/43ACC_OEAW/openurl?u.ignore_date_coverage=true&portfolio_pid=5340568660004498&Force_direct=true |Z 5340568660004498 |b Available |8 5340568660004498 | ||