Echinoderms Metabolites: Structure, Functions and Biomedical Perspectives

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 an...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
अन्य लेखक: Kalinin, Vladimir I. (संपादक)
स्वरूप: इलेक्ट्रोनिक पुस्तक अध्याय
भाषा:अंग्रेज़ी
प्रकाशित: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2021
विषय:
ऑनलाइन पहुंच:DOAB: download the publication
DOAB: description of the publication
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520 |a 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. 
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653 |a prostate cancer 
653 |a thioglucoside conjugates 
653 |a natural products 
653 |a sea urchins 
653 |a glucose uptake 
653 |a polyhydroxysteroidal esters 
653 |a NMR spectra 
653 |a fatty acids 
653 |a starfish 
653 |a Ceramaster patagonicus 
653 |a cytostatic activity 
653 |a soft agar assay 
653 |a wound healing assay 
653 |a Colochirus quadrangularis 
653 |a triterpene glycosides 
653 |a quadrangularisosides 
653 |a sea cucumber 
653 |a cytotoxic activity 
653 |a Holothuria hilla 
653 |a Paracaudina chilensis 
653 |a fucosylated chondroitin sulfate 
653 |a anticoagulant activity 
653 |a echinochrome A 
653 |a echinamine A 
653 |a echinamine B 
653 |a herpes simplex virus type 1 
653 |a Vero cells 
653 |a glycoprotein gD 
653 |a molecular docking 
653 |a Thyonidium kurilensis 
653 |a kurilosides 
653 |a Thenea muricata 
653 |a Aplysina sp. 
653 |a Pseudoanthomastus agaricus 
653 |a Montastraea cavernosa 
653 |a Buccinum sp. 
653 |a Pasiphaea tarda 
653 |a Phormosoma placenta 
653 |a Echinometra lucunter 
653 |a sterols 
653 |a gas chromatography 
653 |a mass spectrometry 
653 |a neuroblastoma Neuro-2a cells 
653 |a 5,8-dihydroxy-1,4-naphthoquinone 
653 |a O-glucoside 
653 |a thiomethylglycoside 
653 |a QSAR 
653 |a n/a 
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