LEADER 03943nam 2200901z- 450 001 9910557386103321 005 20231214133104.0 035 $a(CKB)5400000000042037 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/76851 035 $a(EXLCZ)995400000000042037 100 $a20202201d2021 |y 0 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aEchinoderms Metabolites: Structure, Functions and Biomedical Perspectives 210 $aBasel, Switzerland$cMDPI - Multidisciplinary Digital Publishing Institute$d2021 215 $a1 electronic resource (179 p.) 311 $a3-0365-1594-1 311 $a3-0365-1593-3 330 $aThe 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. 517 $aEchinoderms Metabolites 606 $aMedicine$2bicssc 610 $aprostate cancer 610 $athioglucoside conjugates 610 $anatural products 610 $asea urchins 610 $aglucose uptake 610 $apolyhydroxysteroidal esters 610 $aNMR spectra 610 $afatty acids 610 $astarfish 610 $aCeramaster patagonicus 610 $acytostatic activity 610 $asoft agar assay 610 $awound healing assay 610 $aColochirus quadrangularis 610 $atriterpene glycosides 610 $aquadrangularisosides 610 $asea cucumber 610 $acytotoxic activity 610 $aHolothuria hilla 610 $aParacaudina chilensis 610 $afucosylated chondroitin sulfate 610 $aanticoagulant activity 610 $aechinochrome A 610 $aechinamine A 610 $aechinamine B 610 $aherpes simplex virus type 1 610 $aVero cells 610 $aglycoprotein gD 610 $amolecular docking 610 $aThyonidium kurilensis 610 $akurilosides 610 $aThenea muricata 610 $aAplysina sp. 610 $aPseudoanthomastus agaricus 610 $aMontastraea cavernosa 610 $aBuccinum sp. 610 $aPasiphaea tarda 610 $aPhormosoma placenta 610 $aEchinometra lucunter 610 $asterols 610 $agas chromatography 610 $amass spectrometry 610 $aneuroblastoma Neuro-2a cells 610 $a5,8-dihydroxy-1,4-naphthoquinone 610 $aO-glucoside 610 $athiomethylglycoside 610 $aQSAR 615 7$aMedicine 700 $aKalinin$b Vladimir I$4edt$01327009 702 $aKalinin$b Vladimir I$4oth 906 $aBOOK 912 $a9910557386103321 996 $aEchinoderms Metabolites: Structure, Functions and Biomedical Perspectives$93037790 997 $aUNINA