Synthesis, Study and Utilization of Natural Products
Natural products and the preparations based on them play a stable and ever-increasing role in human and veterinary medicine, agriculture, in food and the cosmetic industry, and in an increasing number of other fields. Their importance is based on the fact that they are mostly bound to renewable sour...
Format: | eBook |
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Language: | English |
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MDPI - Multidisciplinary Digital Publishing Institute
2020
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Online Access: | Open Access: DOAB: description of the publication Open Access: DOAB, download the publication |
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040 | |a oapen |c oapen | ||
041 | 0 | |a eng | |
042 | |a dc | ||
072 | 7 | |a TB |2 bicssc | |
720 | 1 | |a Drasar, Pavel B. |4 aut | |
720 | 1 | |a Khripach, Vladimir A. |4 aut | |
245 | 0 | 0 | |a Synthesis, Study and Utilization of Natural Products |
260 | |b MDPI - Multidisciplinary Digital Publishing Institute |c 2020 | ||
300 | |a 1 online resource (234 p.) | ||
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506 | 0 | |a Open Access |f Unrestricted online access |2 star | |
520 | |a Natural products and the preparations based on them play a stable and ever-increasing role in human and veterinary medicine, agriculture, in food and the cosmetic industry, and in an increasing number of other fields. Their importance is based on the fact that they are mostly bound to renewable sources, which in fact makes them valuable within a circular economy, inter alia. At the same time, natural products provide the origin of stereochemistry, optical activity, regioselectivity, chirality, and many other concepts and directions within science, development, and industry in a scope, which is indispensable. They serve as a constant powerful stimulus and model that inspires researchers to create new effective tools, similar to natural ones, for controlling bioregulation mechanisms and solving practical problems. This was the reason for organizing this Special Issue aimed at underlining the current developments in all the fields connected to natural products. | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by-nc-nd/4.0/ |2 cc |u https://creativecommons.org/licenses/by-nc-nd/4.0/ | ||
546 | |a English | ||
650 | 7 | |a Technology: general issues |2 bicssc | |
653 | |a 4-epi-varioxiranol A | ||
653 | |a absolute structure | ||
653 | |a adhesive | ||
653 | |a anti-inflammation | ||
653 | |a anticancer drug | ||
653 | |a antioxidant | ||
653 | |a antioxidant activity | ||
653 | |a apo-CpcB | ||
653 | |a apoptosis | ||
653 | |a bardoxolone methyl | ||
653 | |a bioactivity | ||
653 | |a biosynthesis | ||
653 | |a bromelain | ||
653 | |a caffeoylquinic acids | ||
653 | |a cancer cells | ||
653 | |a cell opening | ||
653 | |a chlorogenic acid | ||
653 | |a cytotoxicity | ||
653 | |a derivatives | ||
653 | |a Emericella variecolor | ||
653 | |a fatty acid | ||
653 | |a flavonoids | ||
653 | |a flexible polyurethane foam | ||
653 | |a flow cytometry | ||
653 | |a gene expression | ||
653 | |a genetical transformation | ||
653 | |a ginkgolide | ||
653 | |a HepG2 cells | ||
653 | |a inhibitor | ||
653 | |a insect sex pheromone | ||
653 | |a isosorbide | ||
653 | |a lipid-lowering effects | ||
653 | |a live-cell fluorescence microscopy | ||
653 | |a melatonin | ||
653 | |a microbial biosynthesis | ||
653 | |a mitochondria | ||
653 | |a n/a | ||
653 | |a natural enantiomer | ||
653 | |a natural product | ||
653 | |a natural products | ||
653 | |a octadecanoid | ||
653 | |a oleic acid-elicited | ||
653 | |a PEGylated purpurin 18 | ||
653 | |a pharmacokinetic features | ||
653 | |a pharmacological activities | ||
653 | |a phenolic acid | ||
653 | |a photodynamic therapy | ||
653 | |a photosensitizer | ||
653 | |a phototoxicity | ||
653 | |a phycocyanin | ||
653 | |a pinocembrin | ||
653 | |a Plantago depressa | ||
653 | |a platelet-activating factor receptor | ||
653 | |a polyphenol | ||
653 | |a polysaccharides | ||
653 | |a post-translationally modified peptides | ||
653 | |a radical scavenger | ||
653 | |a Ramulus mori | ||
653 | |a research progress | ||
653 | |a resource chemistry | ||
653 | |a reversible urethane linkages | ||
653 | |a rheumatoid arthritis | ||
653 | |a ribosomally synthesized | ||
653 | |a RiPP | ||
653 | |a salt stress | ||
653 | |a singlet oxygen | ||
653 | |a SlCOMT1 | ||
653 | |a soy protein isolate | ||
653 | |a Spirulina | ||
653 | |a stilbene | ||
653 | |a synthesis of natural products | ||
653 | |a tea tussock moth | ||
653 | |a tomato | ||
653 | |a total synthesis | ||
653 | |a triglycidylamine | ||
653 | |a triterpenoids | ||
653 | |a varioxiranol A | ||
653 | |a viscosity | ||
653 | |a water resistance | ||
793 | 0 | |a DOAB Library. | |
856 | 4 | 0 | |u https://directory.doabooks.org/handle/20.500.12854/60411 |7 0 |z Open Access: DOAB: description of the publication |
856 | 4 | 0 | |u https://www.mdpi.com/books/pdfview/book/1975 |7 0 |z Open Access: DOAB, download the publication |