LEADER 04000nam 2200925z- 450 001 9910557386103321 005 20220111 035 $a(CKB)5400000000042037 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/76851 035 $a(oapen)doab76851 035 $a(EXLCZ)995400000000042037 100 $a20202201d2021 |y 0 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aEchinoderms Metabolites: Structure, Functions and Biomedical Perspectives 210 $aBasel, Switzerland$cMDPI - Multidisciplinary Digital Publishing Institute$d2021 215 $a1 online resource (179 p.) 311 08$a3-0365-1594-1 311 08$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 and Nursing$2bicssc 610 $a5,8-dihydroxy-1,4-naphthoquinone 610 $aanticoagulant activity 610 $aAplysina sp. 610 $aBuccinum sp. 610 $aCeramaster patagonicus 610 $aColochirus quadrangularis 610 $acytostatic activity 610 $acytotoxic activity 610 $aechinamine A 610 $aechinamine B 610 $aechinochrome A 610 $aEchinometra lucunter 610 $afatty acids 610 $afucosylated chondroitin sulfate 610 $agas chromatography 610 $aglucose uptake 610 $aglycoprotein gD 610 $aherpes simplex virus type 1 610 $aHolothuria hilla 610 $akurilosides 610 $amass spectrometry 610 $amolecular docking 610 $aMontastraea cavernosa 610 $an/a 610 $anatural products 610 $aneuroblastoma Neuro-2a cells 610 $aNMR spectra 610 $aO-glucoside 610 $aParacaudina chilensis 610 $aPasiphaea tarda 610 $aPhormosoma placenta 610 $apolyhydroxysteroidal esters 610 $aprostate cancer 610 $aPseudoanthomastus agaricus 610 $aQSAR 610 $aquadrangularisosides 610 $asea cucumber 610 $asea urchins 610 $asoft agar assay 610 $astarfish 610 $asterols 610 $aThenea muricata 610 $athioglucoside conjugates 610 $athiomethylglycoside 610 $aThyonidium kurilensis 610 $atriterpene glycosides 610 $aVero cells 610 $awound healing assay 615 7$aMedicine and Nursing 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