Search results for "Natural Compound"

showing 10 items of 26 documents

Indicaxanthin, a multi-target natural compound from Opuntia ficus-indica fruit: From its poly-pharmacological effects to biochemical mechanisms and m…

2019

Abstract Over the latest years phytochemical consumption has been associated to a decreased risk of both the onset and the development of a number of pathological conditions. In this context indicaxanthin, a betalain pigment from Opuntia ficus-indica fruit, has been the object of sound research. Explored, at first, for its mere antioxidant potential, Indicaxanthin is now regarded as a redox-active compound able to exert significant poly-pharmacological effects against several targets in a number of experimental conditions both in vivo and in vitro. This paper aims to provide an overview on the therapeutical effects of indicaxanthin, ranging from the anti-inflammatory to the neuro-modulatory…

Models MolecularPyridinesOpuntia ficusPhytochemicalsContext (language use)Antioxidant potential01 natural sciencesMiceStructure-Activity Relationship03 medical and health scienceschemistry.chemical_compoundMulti targetCell Line TumorNeoplasmsSettore BIO/10 - BiochimicaBetalainDrug DiscoveryAnimalsHumansCell Proliferation030304 developmental biologyInflammationIndicaxanthin Multi-target compound Poly-pharmacology Antioxidant Antiinflammatory Antitumoral Antiproliferative Neuromodulator Molecular modellingPharmacologyBiological Products0303 health sciencesDose-Response Relationship DrugMolecular StructureTraditional medicine010405 organic chemistryNatural compoundOrganic ChemistryOpuntiaGeneral MedicineAntineoplastic Agents PhytogenicSettore CHIM/08 - Chimica FarmaceuticaBetaxanthins0104 chemical sciencesMice Inbred C57BLNeuroprotective AgentsPhytochemicalchemistryBlood-Brain BarrierFruitDrug Screening Assays AntitumorIndicaxanthinEuropean Journal of Medicinal Chemistry
researchProduct

Biomimetic Synthesis of the Apoptosis-Inducing Thiazinoquinone Thiaplidiaquinone A

2012

A concise total synthesis of the apoptosis-inducing, marine metabolite thiaplidiaquinone A is described. The key ring forming steps are both based on biosynthetic considerations and involve the construction of the central benzo[c]chromene quinone unit by an extremely facile oxa-6π-electrocyclic ring closure reaction of an ortho-quinone intermediate, derived by tautomerization of a bis-benzoquinone, readily accessed from two simple phenolic precursors. This is followed by the installation of the 1,4-thiazine-dioxide ring by reaction of the benzo[c]chromene quinone with hypotaurine.

Molecular StructureTerpenesStereochemistryMetaboliteOrganic ChemistryQuinonesTotal synthesisApoptosisHypotaurineThiaplidiaquinone A natural compoundsRing (chemistry)TautomerSettore CHIM/08 - Chimica FarmaceuticaQuinonechemistry.chemical_compoundchemistryBiomimetic MaterialsApoptosisBiomimetic synthesisThiaplidiaquinone A; natural compoundsnatural compoundsThiaplidiaquinone A
researchProduct

Ultrasound-assisted extraction for food and environmental samples

2013

Abstract In recent years, ultrasound-assisted extraction (UAE) has attracted growing interest, as it is an effective method for the rapid extraction of a number of compounds from food and environmental samples, with extraction efficiency comparable to that of classical techniques. In particular, recently, numerous analytical applications of this technique dealt with the extraction of natural compounds and pollutants from food and environmental samples. This review gives a brief presentation of the theory of UAE, discusses recent advances that influence its efficiency, and summarizes the main results in selected applications published in the period 2010–12. There is discussion of the advanta…

Natural compoundEnvironmental chemistryExtraction (chemistry)Environmental scienceFood sampleBiochemical engineeringUltrasound assistedSpectroscopyAnalytical ChemistryTrAC Trends in Analytical Chemistry
researchProduct

Photoinduced functionalization of diterpenes: photochemical behaviour of grandifloric acid in methanol and acetonitrile

2004

Abstract Irradiation of grandiflorolic acid (11) at λ=254 nm in acetonitrile gave the two epimers 13 and 14 through a photodecarboxylation reaction of the carboxylic group on C-4. Irradiation of compound 11 in methanol at λ=254 nm provided the transformation of the C-20 angular methyl into a carbomethoxymethyl group. In this case, unlike compounds 13 and 14, only one of the two possible isomers (15) was obtained (equatorial methyl at C-4). A mechanistic approach of this reaction in discussed, and the role of mutual stereochemistry between C-20 methyl and C-19 carboxylic group in determining the course of the reaction is pointed out.

PhotochemistryGeneral Chemical EngineeringCarboxylic groupGeneral Physics and AstronomyGeneral ChemistrySettore CHIM/06 - Chimica OrganicaNatural compoundPhotochemistrychemistry.chemical_compoundGrandiflorolic acidchemistrySurface modificationEpimerMethanolIrradiationGrandiflorolic acidAcetonitrileDiterpene
researchProduct

Synthesis of natural polyhydroxystilbenes

1986

Synthese en particulier de pinosylvine, isorhapontigenine, piceatannol et du methoxy-4 stilbenetetraol-3,3',5,5'

Piceatannolchemistry.chemical_compoundchemistryPolyphenolStereochemistryNatural compoundOrganic ChemistryDrug DiscoveryWittig reactionPhoenix dactyliferaOrganic chemistryBiochemistryTetrahedron
researchProduct

Countercurrent chromatography: People and applications

2009

The scientific literature was scanned for the published research articles dealing with countercurrent chromatography (CCC) over the time period 1980-May 2008. The search returned 1638 articles that were analyzed focussing on people and applications. Concerning the people, it was found that the geographical location of the CCC authors was relatively well balanced between USA, Asia with mainly China and Japan and Europe. Yoichiro Ito, the inventor of the technique, is by far the most productive author in the field with 331 articles or more than one over five CCC articles published in the time period. Without surprise, English is the dominant language with more than 82% of the articles. A sign…

PublishingBiological ProductsSubject HeadingsChromatographyImpact factorChemistryNatural compoundOrganic ChemistryGeneral MedicineScientific literatureBibliometricsBiochemistryAuthorshipAnalytical ChemistryImpact indexCountercurrent chromatographyBibliometricsJournal Impact FactorPeriodicals as TopicCountercurrent distributionCountercurrent DistributionJournal of Chromatography A
researchProduct

H(II) centers in natural silica under repeated UV laser irradiations

2004

We investigated the kinetics of H(II) centers (=Ge'-H) in natural silica under repeated 266nm UV irradiations performed by a Nd:YAG pulsed laser. UV photons temporarily destroy these paramagnetic defects, their reduction being complete within 250 pulses. After re-irradiation, H(II) centers grow again, and the observed recovery kinetics depends on the irradiation dose; multiple 2000 pulses re-irradiations induce the same post-irradiation kinetics of H(II) centers after each exposure cycle. The analysis of these effects allows us to achieve a deeper understanding of the dynamics of the centers during and after laser irradiation.

Pulsed laserKineticsTWOFOLD COORDINATED SIFOS: Physical sciencesATOMSParamagnetismMaterials ChemistryUv laserIrradiationEXPOSUREQuartzCondensed Matter - Materials ScienceSNChemistryNatural compoundRadiochemistryMaterials Science (cond-mat.mtrl-sci)Disordered Systems and Neural Networks (cond-mat.dis-nn)DEFECTSCondensed Matter - Disordered Systems and Neural NetworksCondensed Matter PhysicsDIFFUSIONElectronic Optical and Magnetic MaterialsWavelengthGE-DOPED SIO2MOLECULAR-HYDROGENGLASSESCeramics and Composites
researchProduct

Priming of plant resistance by natural compounds. Hexanoic acid as a model

2014

Some alternative control strategies of currently emerging plant diseases are based on the use of resistance inducers. This review highlights the recent advances made in the characterization of natural compounds that induce resistance by a priming mechanism. These include vitamins, chitosans, oligogalacturonides, volatile organic compounds, azelaic and pipecolic acid, among others. Overall, other than providing novel disease control strategies that meet environmental regulations, natural priming agents are valuable tools to help unravel the complex mechanisms underlying the induced resistance (IR) phenomenon. The data presented in this review reflect the novel contributions made from studyin…

Review ArticlePriming (agriculture)Plant ScienceBiologylcsh:Plant culturechemistry.chemical_compoundBotrytis cinereaAlternative controlHost plantsnatural inducersoxidative stresslcsh:SB1-1110primingPipecolic acidHexanoic acidbusiness.industryNatural compoundCalloseVitaminsvitaminsDisease controlBiotechnologychemistryBiochemistryPrimingOxidative stressHexanoic acidbusinesshexanoic acidNatural inducersFrontiers in Plant Science
researchProduct

Novel scaffold of natural compound eliciting sweet taste revealed by machine learning

2020

Abstract Sugar replacement is still an active issue in the food industry. The use of structure-taste relationships remains one of the most rational strategy to expand the chemical space associated to sweet taste. A new machine learning model has been setup based on an update of the SweetenersDB and on open-source molecular features. It has been implemented on a freely accessible webserver. Cellular functional assays show that the sweet taste receptor is activated in vitro by a new scaffold of natural compounds identified by the in silico protocol. The newly identified sweetener belongs to the lignan chemical family and opens a new chemical space to explore.

ScaffoldsweetenerComputer scienceIn silicoMachine learningcomputer.software_genre01 natural sciencesAnalytical ChemistryReceptors G-Protein-Coupled0404 agricultural biotechnologysweet tastenatural compoundsHumans[CHIM]Chemical Sciences[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biologysweet taste receptor2. Zero hungerbusiness.industryNatural compound010401 analytical chemistrydigestive oral and skin physiologySweet taste04 agricultural and veterinary sciencesGeneral Medicine040401 food scienceChemical space0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrymachine learningSweetening AgentsTasteArtificial intelligencebusinesscomputer[CHIM.CHEM]Chemical Sciences/CheminformaticsFood Science
researchProduct

Natural compounds as light stabilizer for a starch-based biodegradable polymer

2014

Abstract The photooxidation behavior of a commercial starch-based biodegradable polymer, i.e., new generation Mater-Bi, loaded with natural stabilizers was investigated in consideration for outdoor agricultural applications. The photooxidation behavior of the biodegradable films was monitored mainly by mechanical tests and spectroscopic analysis. In order to formulate biodegradable films without any synthetic compounds, suitable for outdoor applications and with good photooxidation stability, antioxidants such as α-tocopherol and quercetin (Q) were considered. The results obtained using natural compounds were compared with those obtained by using a synthetic antioxidant and a light stabiliz…

chemistry.chemical_classificationphoto-oxidation behaviorMaterials sciencePolymers and PlasticsPolymer scienceStarchGeneral Chemical EngineeringIndustrial chemistryPolymerBiodegradable polymerstarch-based biodegradable filmnatural compoundchemistry.chemical_compoundchemistryMaterials Chemistrylight stabilizerComposite materialMater-Bi®Stabilizer (chemistry)Journal of Polymer Engineering
researchProduct