Book ; Online: Coumarin and Its Derivatives
2021
Keywords | Research & information: general ; Biology, life sciences ; coumarin ; hydroxyl-modified coumarin ; photophysical ; thermal and structural characterization ; Glycyrrhiza uralensis ; glycyrol ; liquiritigenin ; cholinesterases ; human monoamine oxidases ; kinetics ; docking simulation ; chalcone ; neurodegenerative diseases ; adenosine receptors ; binding affinity ; docking ; 4-hydroxy-7-methoxycoumarin ; macrophage ; inflammation ; NF-κB ; MAPK ; calanolides ; pseudocalanolides ; calanolide A ; Calophyllum ; Calophyllaceae ; anti-HIV ; reverse transcriptase ; non-nucleoside reverse transcriptase inhibitors (NNRTIs) ; osthole ; umbelliferone ; esculin ; 4-hydroxycoumarin ; sorafenib ; apoptosis ; autophagy ; Yin Chen Hao ; constitutive androstane receptor ; scoparone ; coumarins ; quorum sensing ; QS inhibitors ; plant-derived molecules ; Chromobacterium violaceum ; immunoproteasome ; psoralen core ; non-peptidic ; electrophilic compounds ; warhead scan ; inflammatory bowel disease ; isocoumarin ; Crohn's disease ; ulcerative colitis ; glutathione ; oxidative stress ; complementary therapies ; intestinal inflammation ; benzopyrones ; five-membered aromatic heterocycles ; furan ; pyrrole ; thiophene ; selenophen ; dihydrocoumarin-fused dihydropyranones ; 3-aroylcoumarines ; benzyl 2,3-butadienoate ; 6'-(4-biphenyl)-β-iso-cinchonine ; biological applications ; drug discovery ; fluorescent probes ; warfarin ; acenocoumarol ; mechanical valve ; time in therapeutic range ; anticoagulation ; Ruta chalepensis ; Rutaceae ; chalepin ; chalepensin ; bioactivity ; biosynthesis ; coumarin3-carboxamides ; pyranocoumarins ; anticancer activity ; antibacterial activity ; free radical polymerization ; LED ; photocomposites ; direct laser write ; analytical methods ; model plant ; natural genetic variation ; natural products ; simple coumarins ; chalcocoumarin ; MAO-B ; molecular dynamics ; in silico studies ; dye-sensitized solar cells ; coumarin dyes ; thieno [3,2-b] thiophene ; charge transfer ; ethynylaryl ; esculetin ; antiplatelet activity ; impedance aggregometry ; COX ; polyphenols ; pyrazole ; imidazole ; thiazole ; oxazole ; triazole ; thiadiazole ; curcumin ; curcumin-coumarin hybrids ; neuroprotection ; monoamine oxidase inhibition ; cholinesterase inhibition ; scavenging activity ; Escherichia coli ; biotransformation ; ferulenol ; structural annotation ; in silico tools ; n/a |
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Size | 1 electronic resource (406 pages) |
Publisher | MDPI - Multidisciplinary Digital Publishing Institute |
Publishing place | Basel, Switzerland |
Document type | Book ; Online |
Note | English ; Open Access |
HBZ-ID | HT021291115 |
ISBN | 9783036527741 ; 3036527745 |
Database | ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture |
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