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Biological Activity and Applications of Natural Compounds
| Biological Activity and Applications of Natural Compounds |
| Autore | Seca Ana M. L |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 online resource (206 p.) |
| Soggetto topico | Medicine |
| Soggetto non controllato |
5-pentylcyclohexa-1,3-diene
alantolactone aldol condensation almond amino acid metabolism anti-aging anti-inflammatory antibacterial activity anticancer anticholinesterase antidiabetic antidiabetic activity antimicrobial antioxidant antitumor apoptosis arglabin Aspergillus niger Asteraceae biological activity byproducts Caenorhabditis elegans Candida Candida albicans cardioprotective carvacrol celastroloids chalcones chlorogenic acid colorectal cancer Cryptococcus neoformans cytotoxic design of experiment essential oils flavanones flavonoid fungistatic effect GC/MS Helianthus annuus Helianthus strumosus honey in vivo study inhibition of dimorphism longevity Maytenus metabolomics data natural compounds NHDF cells oleracone osthole oxidative stress parthenolide Penicillium digitatum phenolic acids phenolic compounds pimenta d'água Portulaca oleracea L. Prangos pabularia Lindl propolis PTP-1B rosemary rosmarinic acid Salviae miltiorrhizae radix SAR semisynthesis sesquiterpene lactones structure-activity relationship thapsigargin therapeutic applications total synthesis ultrasound-assisted extraction volatile oil wound-healing activity α-pinene |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557291403321 |
Seca Ana M. L
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Catalyzed Synthesis of Natural Products
| Catalyzed Synthesis of Natural Products |
| Autore | Díez David |
| Pubbl/distr/stampa | MDPI - Multidisciplinary Digital Publishing Institute, 2019 |
| Descrizione fisica | 1 online resource (82 p.) |
| Soggetto topico | Chemistry |
| Soggetto non controllato |
?-amination
3-hydroxyoxindole acidolysis aminocatalysis antcin K anticancer Antrodia cinnamomea asymmetric catalysis asymmetric organocatalysis benzimidazole biotransformation carvone chiral ?-hydroxyamide deep eutectic solvents egg-yolk phosphatidylcholine epoxidation epoxide green chemistry immobilized lipases interesterification isatin mandelamides myristic acid n/a natural products organocatalysis phaeosphaeride A phaeosphaeride B proline Psychrobacillus STAT3 structural revision structured phosphatidylcholine total synthesis trimyristin triterpenoid zinc |
| ISBN | 3-03921-949-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910367737103321 |
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Díez David
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| MDPI - Multidisciplinary Digital Publishing Institute, 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Discovery and Total Synthesis of Bio-functional Natural Products from Traditional Medicinal Plants
| Discovery and Total Synthesis of Bio-functional Natural Products from Traditional Medicinal Plants |
| Autore | Wang Tao |
| Pubbl/distr/stampa | Frontiers Media SA, 2020 |
| Descrizione fisica | 1 online resource (99 p.) |
| Soggetto topico | Science: general issues |
| Soggetto non controllato |
bioorganic chemistry
isolation natural products chemistry phytochemistry structural determination total synthesis |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557582603321 |
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Wang Tao
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| Frontiers Media SA, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Lignans / David Barker
| Lignans / David Barker |
| Autore | Barker David |
| Pubbl/distr/stampa | MDPI - Multidisciplinary Digital Publishing Institute, 2019 |
| Descrizione fisica | 1 electronic resource (384 p.) |
| Soggetto topico | Chemistry |
| Soggetto non controllato |
taste-active compound
heilaohu 9-norlignans antioxidant activity drug-like human health chemometrics lignan bitterness red-flowered Chinese magnolia vine antioxidant ruminant secoisolariciresinol diglucoside quantification intermolecular interactions cattle anti-inflammatory activity acyl-Claisen LOX seed food groups microtubules anti-proliferative acetylcholinesterase inhibitors flax arylnaphthalene lignan epiboly aryldihydronaphthalene lignan multiple bioactive components enterolignan total synthesis genetic synthesis cultivated cell cycle chronic diseases national databases oxidation chemical components molecular dynamics COX lignans hydroxycinnamic acid chemical structures Chinese magnolia vine stereoselective synthesis sPLA2 Bursera fagaroides in silico studies antibacterial activity semisynthesis dibenzyl butyrolactones flavonoid glycoside lignan glycoside chemical characterization hydroxymatairesinol podophyllotoxin Lespedeza cuneata Bursera oak ageing Schisandrae Chinensis Fructus F-actin cultivar UHPLC-MS/MS bioactivity podophyllotoxin-type lignans harmonized databases graph theory antioxidants health promotion simultaneous quantitation natural products dietary intake cell migration Lignan chemical space diet Lauraceae pharmacokinetic cytotoxicity tujia ethnomedicine flavonolignans flavonol adipocyte and osteoblast differentiation Burseraceae environment dietary lignans phytochemical analysis Schisandra chinensis animal health neolignans Schisandra rubriflora cancer norlignans wild |
| ISBN |
9783038979098
3038979090 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910346692503321 |
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Barker David
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| MDPI - Multidisciplinary Digital Publishing Institute, 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Marine Natural Products as Anticancer Agents
| Marine Natural Products as Anticancer Agents |
| Autore | Alves Celso |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (150 p.) |
| Soggetto topico | Medicine and Nursing |
| Soggetto non controllato |
alga
anti-cancer antitumor aplysinopsin analogs apoptosis astaxanthin BH3 mimetics bioactive compounds biscembranoid-type metabolites BT20 cancer stem cells cancer therapy chronic myeloid leukemia colony formation cytotoxicity Ehlich's tumor environment epigenetic signaling epigenome epithelial-mesenchymal transition flaccidoxide-13-acetate gram-scale hepatocellular carcinoma hydroxyphenylacetic acid indole alkaloids inflammation inflammatory factor production invasion LPS-stimulated murine macrophage marine source marine species marine-derived fungus meroterpenoids migration mutp53 n/a nannocystin Nanog natural product Oct4 P. purpurogenum Penicillium chrysogenum polyketide pontin proliferation prostate cancer Sarcophyton digitatum secondary metabolites siRNA STAT3 T47D total synthesis |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557595603321 |
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Alves Celso
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Modern Strategies for Heterocycle Synthesis
| Modern Strategies for Heterocycle Synthesis |
| Autore | Favi Gianfranco |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (372 p.) |
| Soggetto topico | Medicine |
| Soggetto non controllato |
1-oxa-triene
1,2,3-triazol 1,3-oxazines 1H-imidazole-2(3H)-thione 2H-imidazo[2,1-b][1,3,4]thiadiazine 2H-pyran 3-trifluoroacetyl coumarins 3,2':6',3"-terpyridine 4-bromo quinolines 5-acylamino-1,3-thiazoles acylhydrazone group alkynes alkynoic acids amine nucleophiles antifungal activities antitumor aromatic substitution arylation asymmetric dimeric β-carboline aza-Wittig azides cascade cyclization cascade reaction CF3CO-acetylenes cinnolines click reaction condensation copper-catalyzed azide-alkyne cycloaddition coumarin CuAAC cyclic ethers cycloalkynes cyclohexanol derivative cycloisomerization cytotoxic cytotoxicity dienone dihydrocoumarins enol ethers fluorescence fluorinated heterocycles fluoroalcohol fused N-heterocycles gold catalysis Hantzsch reaction heterocycles heterocyclic inter-molecular approach intra-molecular approach ketone Knoevenagel multicomponent reaction multicomponent reactions n/a natural products nucleobase organic dyes organocatalysis oxa-electrocyclization phenols photocatalysis photoredox photoredox cyclization propargyl Claisen propargylic alcohols purine pyrazolo[3,4-b]pyridine pyridine pyrrolidones Richter cyclization saturated oxygen heterocycles silica sulfuric acid solid-phase synthesis Staudinger reaction structure-activity relationship Suzuki coupling synthesis synthesis of benzofurans terpyridines TMSBr total synthesis traceless synthesis triazoles triazolylmethyl phosphate triazolylmethyl phosphinate valence isomerism visible-light-induced catalysis α-chloroglycinates α-halohydrazones γ-lactam |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557409903321 |
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Favi Gianfranco
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Nitro Compounds and Their Derivatives in Organic Synthesis
| Nitro Compounds and Their Derivatives in Organic Synthesis |
| Autore | Nishiwaki Nagatoshi |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 online resource (120 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
1-methyl-2-quinolone
1,3-dicarbonyl compound 1,3-Dipole 1,4-dihydropyridines 8-nitro-5-RO-indolizines anchimeric assistance aromaticity C-H functionalization conjugate addition cycloaddition dearomatization Diels-Alder reaction dihydrofuran direct functionalization electron-withdrawing ability electrophilicity enolate epimerization hexapyrrolohexaazacoronene ICT character isoxazoline N-oxide isoxazolo[4,3-b]pyridines nitration nitro nitro group nitroketone nitronate nitropyridines nucleophilic addition nucleophilic substitution nucleophilicity organic materials oxazole-pyrrole ring transformation PDE4 inhibitors perylenediimide Phenacylation of beta-nitropyridin-2-ones pyridone pyrrolidines SNAr substitution total synthesis |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557494003321 |
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Nishiwaki Nagatoshi
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances
| Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances |
| Autore | Manzo Emiliano |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (147 p.) |
| Soggetto topico | Language and Linguistics |
| Soggetto non controllato |
7-deazapurine nucleoside
alkylglycerol (AKG) amides/esters antibacterial iminosugars antibiotics (gentamicin antimicrobial activity antiproliferative activity apoptosis aureol bioactive diterpenes bis-indoles breast cancer carbohydrates cholesterol ciprofloxacin and ampicillin) COVID-19 cytostatic disaccharide nucleoside fluoro olefin fucose fucosylated chondroitin sulfate G0/G1 cell-cycle arrest glycosylation HDAC inhibitors labdane scaffold largazole lipophilic iminosugars marine natural product marine-inspired meroterpenoids modification n/a natural product natural products synthesis organic synthesis polymer-supported triphenyl phosphine polysaccharides ricinoleic acid (RA) SARS-CoV-2 sclareolide semi-synthesis solid tumor cell lines structure-activity relationship (SAR) studies structure-activity relationships sulfation synthesis tetracyclic meroterpenoids tetracycline thiazinoquinones total synthesis TRPV4 channel tubercidin |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557681103321 |
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Manzo Emiliano
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances II
| Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances II |
| Autore | Manzo Emiliano |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (111 p.) |
| Soggetto topico |
Chemistry
Research & information: general |
| Soggetto non controllato |
(−)-majusculoic acid
ADMET animal studies anti-inflammation aureol Avicennia alba biological activity biosynthesis cancer cardiovascular diseases CCK-8 chemical synthesis cyclomarins cyclopeptides divergent total synthesis gag polyprotein homology modeling ilamycins In-silico drug design inflammation LPS malaria marine alkaloids marine natural products molecular dynamics simulation n/a natural products rufomycins tetracyclic meroterpenoids total synthesis tuberculosis virtual screening |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557724503321 |
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Manzo Emiliano
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Synthesis, Study and Utilization of Natural Products
| Synthesis, Study and Utilization of Natural Products |
| Autore | Drasar Pavel B |
| Pubbl/distr/stampa | MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 online resource (234 p.) |
| Soggetto topico | Technology: general issues |
| Soggetto non controllato |
4-epi-varioxiranol A
absolute structure adhesive anti-inflammation anticancer drug antioxidant antioxidant activity apo-CpcB apoptosis bardoxolone methyl bioactivity biosynthesis bromelain caffeoylquinic acids cancer cells cell opening chlorogenic acid cytotoxicity derivatives Emericella variecolor fatty acid flavonoids flexible polyurethane foam flow cytometry gene expression genetical transformation ginkgolide HepG2 cells inhibitor insect sex pheromone isosorbide lipid-lowering effects live-cell fluorescence microscopy melatonin microbial biosynthesis mitochondria n/a natural enantiomer natural product natural products octadecanoid oleic acid-elicited PEGylated purpurin 18 pharmacokinetic features pharmacological activities phenolic acid photodynamic therapy photosensitizer phototoxicity phycocyanin pinocembrin Plantago depressa platelet-activating factor receptor polyphenol polysaccharides post-translationally modified peptides radical scavenger Ramulus mori research progress resource chemistry reversible urethane linkages rheumatoid arthritis ribosomally synthesized RiPP salt stress singlet oxygen SlCOMT1 soy protein isolate Spirulina stilbene synthesis of natural products tea tussock moth tomato total synthesis triglycidylamine triterpenoids varioxiranol A viscosity water resistance |
| ISBN | 3-03928-153-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910372783503321 |
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Drasar Pavel B
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| MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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