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...
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| Format: | Electronic Book Chapter |
| Language: | English |
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MDPI - Multidisciplinary Digital Publishing Institute
2020
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| Online Access: | DOAB: download the publication DOAB: description of the publication |
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| 024 | 7 | |a 10.3390/books978-3-03928-153-4 |c doi | |
| 041 | 0 | |a eng | |
| 042 | |a dc | ||
| 072 | 7 | |a TB |2 bicssc | |
| 100 | 1 | |a Drasar, Pavel B. |4 auth | |
| 700 | 1 | |a Khripach, Vladimir A. |4 auth | |
| 245 | 1 | 0 | |a Synthesis, Study and Utilization of Natural Products |
| 260 | |b MDPI - Multidisciplinary Digital Publishing Institute |c 2020 | ||
| 300 | |a 1 electronic resource (234 p.) | ||
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| 506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
| 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 |4 https://creativecommons.org/licenses/by-nc-nd/4.0/ | ||
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| 650 | 7 | |a Technology: general issues |2 bicssc | |
| 653 | |a varioxiranol A | ||
| 653 | |a natural enantiomer | ||
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| 653 | |a ribosomally synthesized | ||
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| 653 | |a apo-CpcB | ||
| 653 | |a water resistance | ||
| 653 | |a radical scavenger | ||
| 653 | |a bardoxolone methyl | ||
| 653 | |a antioxidant activity | ||
| 653 | |a octadecanoid | ||
| 653 | |a derivatives | ||
| 653 | |a inhibitor | ||
| 653 | |a chlorogenic acid | ||
| 653 | |a biosynthesis | ||
| 653 | |a microbial biosynthesis | ||
| 653 | |a flow cytometry | ||
| 653 | |a adhesive | ||
| 653 | |a phycocyanin | ||
| 653 | |a antioxidant | ||
| 653 | |a anticancer drug | ||
| 653 | |a resource chemistry | ||
| 653 | |a ginkgolide | ||
| 653 | |a anti-inflammation | ||
| 653 | |a salt stress | ||
| 653 | |a polyphenol | ||
| 653 | |a synthesis of natural products | ||
| 653 | |a rheumatoid arthritis | ||
| 653 | |a PEGylated purpurin 18 | ||
| 653 | |a photosensitizer | ||
| 653 | |a RiPP | ||
| 653 | |a isosorbide | ||
| 653 | |a bioactivity | ||
| 653 | |a cell opening | ||
| 653 | |a stilbene | ||
| 653 | |a tea tussock moth | ||
| 653 | |a flavonoids | ||
| 653 | |a flexible polyurethane foam | ||
| 653 | |a gene expression | ||
| 653 | |a genetical transformation | ||
| 653 | |a research progress | ||
| 653 | |a oleic acid-elicited | ||
| 653 | |a pharmacokinetic features | ||
| 653 | |a phenolic acid | ||
| 653 | |a Plantago depressa | ||
| 653 | |a platelet-activating factor receptor | ||
| 653 | |a photodynamic therapy | ||
| 653 | |a fatty acid | ||
| 653 | |a soy protein isolate | ||
| 653 | |a apoptosis | ||
| 653 | |a HepG2 cells | ||
| 653 | |a cancer cells | ||
| 653 | |a live-cell fluorescence microscopy | ||
| 653 | |a tomato | ||
| 653 | |a caffeoylquinic acids | ||
| 653 | |a pinocembrin | ||
| 653 | |a insect sex pheromone | ||
| 653 | |a 4-epi-varioxiranol A | ||
| 653 | |a natural products | ||
| 653 | |a singlet oxygen | ||
| 653 | |a total synthesis | ||
| 653 | |a lipid-lowering effects | ||
| 653 | |a reversible urethane linkages | ||
| 653 | |a cytotoxicity | ||
| 653 | |a bromelain | ||
| 653 | |a Ramulus mori | ||
| 653 | |a polysaccharides | ||
| 653 | |a SlCOMT1 | ||
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| 653 | |a Emericella variecolor | ||
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| 653 | |a post-translationally modified peptides | ||
| 653 | |a phototoxicity | ||
| 653 | |a melatonin | ||
| 856 | 4 | 0 | |a www.oapen.org |u https://www.mdpi.com/books/pdfview/book/1975 |7 0 |z DOAB: download the publication |
| 856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/60411 |7 0 |z DOAB: description of the publication |