Isolation, Structure Elucidation and Biological Activity of Natural Products

This Issue focuses on processes related to the research of natural products dereived from plants (Bauhinia forficata, Placolobium vietnamense, Tamarix chinensis, Peperomia obtusifolia, Cymbidium ensifolium, Dendrobium delacourii, Turnera subulata, Eruca sativa, Miconia chamissois and Persea american...

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Other Authors: Takahashi, Jacqueline Aparecida (Editor)
Format: Electronic Book Chapter
Language:English
Published: Basel MDPI - Multidisciplinary Digital Publishing Institute 2023
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DOAB: description of the publication
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245 1 0 |a Isolation, Structure Elucidation and Biological Activity of Natural Products 
260 |a Basel  |b MDPI - Multidisciplinary Digital Publishing Institute  |c 2023 
300 |a 1 electronic resource (386 p.) 
336 |a text  |b txt  |2 rdacontent 
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520 |a This Issue focuses on processes related to the research of natural products dereived from plants (Bauhinia forficata, Placolobium vietnamense, Tamarix chinensis, Peperomia obtusifolia, Cymbidium ensifolium, Dendrobium delacourii, Turnera subulata, Eruca sativa, Miconia chamissois and Persea americana) and microorganisms (Streptomyces tricolor, Lacticaseibacillus rhamnosus, Gonatophragmium triuniae, Penicillium bissettii and P. glabrum) as well as spectroscopic data from a significant number of natural products, 13C-NMR data from 504 pentacyclic triterpenoids isolated from plants of the Celastraceae family and UV, IR, 1H and 13C-NMR data of the 192 chromones. 
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 Technology: general issues  |2 bicssc 
650 7 |a Biotechnology  |2 bicssc 
653 |a chromone glycosides 
653 |a chemical structure 
653 |a activity 
653 |a benzo-γ-pyrone 
653 |a 13C-NMR data 
653 |a antimicrobial 
653 |a penicillium 
653 |a metabolite 
653 |a fungi 
653 |a natural products 
653 |a Gonatophragmium triuniae 
653 |a pigments 
653 |a bioactivity 
653 |a dyeing 
653 |a chemical characterization 
653 |a biosynthesis 
653 |a macrolides 
653 |a peptides 
653 |a polyketides 
653 |a secondary metabolites 
653 |a Streptomyces 
653 |a structure elucidation 
653 |a terpenoids 
653 |a Celastraceae 
653 |a triterpenes 
653 |a quinonemethide 
653 |a 13C-NMR 
653 |a plant 
653 |a natural compounds 
653 |a chromatography 
653 |a anti-inflammatory 
653 |a Miconia chamissois Naudin 
653 |a seasonality 
653 |a standardized extract 
653 |a Cerrado 
653 |a Dendrobium delacourii 
653 |a Orchidaceae 
653 |a α-glucosidase 
653 |a anti-adipogenic 
653 |a densifloral B 
653 |a phoyunnanin E 
653 |a phoyunnanin C 
653 |a glucosinolate 
653 |a glucosylated flavonols 
653 |a rocket 
653 |a validation 
653 |a NMR 
653 |a UHPLC/ESI/QTOF 
653 |a hyperuricaemia 
653 |a avocado biomass 
653 |a Alzheimer's disease 
653 |a neuroprotective effect 
653 |a avocado seed 
653 |a avocado peel 
653 |a paper spray mass spectrometry 
653 |a Lacticaseibacillus rhamnosus 
653 |a yak yoghurt 
653 |a antibacterial activity 
653 |a purification 
653 |a bacteriocin 
653 |a Cymbidium ensifolium 
653 |a dihydrophenanthrene 
653 |a dihydrophenanthrenequinone 
653 |a anticancer 
653 |a Streptomyces tricolor 
653 |a siderophore 
653 |a iron-deficiency-induced anemia 
653 |a Piperaceae 
653 |a Peperomia obtusifolia 
653 |a isolation 
653 |a cytotoxicity 
653 |a antibacterial 
653 |a Tamarix chinensis Lour. 
653 |a flavonoid substituted polysaccharides 
653 |a structural characterization 
653 |a anticomplement activity 
653 |a quercetin 
653 |a Placolobium vietnamense 
653 |a placovinones A-D 
653 |a benzil and isoflavone derivatives 
653 |a NO production inhibition 
653 |a "pata-de-vaca" 
653 |a phytochemical profile 
653 |a bioactive compounds 
653 |a antioxidant capacity 
653 |a α-amylase inhibition 
653 |a SPME technique 
653 |a n/a 
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856 4 0 |a www.oapen.org  |u https://directory.doabooks.org/handle/20.500.12854/128645  |7 0  |z DOAB: description of the publication