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...
में बचाया:
अन्य लेखक: | |
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स्वरूप: | इलेक्ट्रोनिक पुस्तक अध्याय |
भाषा: | अंग्रेज़ी |
प्रकाशित: |
Basel, Switzerland
MDPI - Multidisciplinary Digital Publishing Institute
2021
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विषय: | |
ऑनलाइन पहुंच: | DOAB: download the publication DOAB: description of the publication |
टैग: |
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100 | 1 | |a Kalinin, Vladimir I. |4 edt | |
700 | 1 | |a Kalinin, Vladimir I. |4 oth | |
245 | 1 | 0 | |a Echinoderms Metabolites: Structure, Functions and Biomedical Perspectives |
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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. | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
546 | |a English | ||
650 | 7 | |a Medicine |2 bicssc | |
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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856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/76851 |7 0 |z DOAB: description of the publication |