Search results for "natural product"

showing 10 items of 163 documents

Semisynthesis of the Antiviral Abietane Diterpenoid Jiadifenoic Acid C from Callitrisic Acid (4-Epidehydroabietic Acid) Isolated from Sandarac Resin

2014

The semisynthesis of the antiviral abietane diterpenoid (+)-jiadifenoic acid C starting from the available methyl ester of callitrisic acid (4-epidehydroabietic acid) isolated from sandarac resin is reported. A protocol for the isolation of methyl callitrisate (methyl 4-epidehydroabietate) in gram quantities from sandarac resin is also described. Allylic C-17 oxygenation was introduced by regioselective dehydrogenation of the isopropyl group of methyl callitrisate with DDQ followed by selenium-catalyzed allylic oxidation. Ester hydrolysis afforded (+)-jiadifenoic acid C in 22% overall yield from methyl callitrisate. This semisynthetic route provides a convenient source of this anti-Coxsacki…

PharmacologyAllylic rearrangementNatural productMolecular StructureChemistryOrganic ChemistrySandaracPharmaceutical ScienceRegioselectivityAntiviral AgentsSemisynthesisTerpenoidEnterovirus B HumanAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicineAbietanesDrug DiscoveryMolecular MedicineOrganic chemistryNuclear Magnetic Resonance BiomolecularOxidation-ReductionResins PlantIsopropylAbietaneJournal of Natural Products
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Structure and Biological Activity of the Furan-Diterpenoids from the Genera Leonotis and Leonurus

2007

The present review, covering the literature up to 2006, reports the chemistry and the biological activities of the diterpenoids occurring in the aerial parts of species belonging to the genera Leonotis and Leonurus, family Lamiaceae.

PharmacologyFamily Lamiaceaenatural productLeonurusLeonuruNatural productbiologyOrganic Chemistrybiological activityBiological activitybiology.organism_classificationAnalytical ChemistryLabdanechemistry.chemical_compoundchemistryFuranLeonotiBotanyLabdaneLeonotisHETEROCYCLES
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Acid Rearrangment of Epoxy-germacranolides and Absolute Configuration of 1β,10α-Epoxy-salonitenolide

2010

The acid-catalyzed cyclization of mono epoxides of cnicin acetonide (3) was investigated. Several 6,12-eudesmanolides were obtained, and their stereochemistry established by extensive spectroscopic analyses. Chemical correlations also led to the assignment of the absolute configuration of 1β,10α-epoxy-salonitenolide (13), a previously isolated natural product. The cytotoxic activities of some compounds were determined against A549 and MCF-7 tumor cell lines. The esterified germacranolides 2–6 were selectively cytotoxic against the MCF-7 breast cancer cell line.

PharmacologyNatural productStereochemistryAbsolute configurationSalonitenolidePlant ScienceGeneral MedicineEpoxyAcetonideCnicinchemistry.chemical_compoundComplementary and alternative medicineBreast cancer cell linechemistryvisual_artDrug Discoveryvisual_art.visual_art_mediumOrganic chemistryCytotoxicityNatural Product Communications
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Phytotoxic dioxolanone-type secondary metabolites from Guignardia bidwellii.

2012

Phenguignardic acid was recently described as a phytotoxic secondary metabolite from submerged cultures of the grape black rot fungus Guignardia bidwellii. Since the production rate of this natural product in submerged culture is very low, fermentation optimisation was carried out. The optimisation of cultivation conditions led to the identification of seven secondary metabolites, structurally related to guignardic acid, a known secondary metabolite from Guignardia species containing a dioxolanone moiety. All metabolites presented here have not been described to date and are presumably biosynthesised via deamination products of amino acids, such as phenylalanine, valine, tyrosine, and alani…

PhenylalanineGuignardiaPlant ScienceHorticultureBiologySecondary metaboliteBiochemistrychemistry.chemical_compoundAscomycotaValinemedicineVitisMolecular BiologyAlaninechemistry.chemical_classificationNatural productTemperatureDioxolanesGeneral MedicineHydrogen-Ion Concentrationbiology.organism_classificationAmino acidBiochemistrychemistryFermentationFermentationmedicine.drugPhytochemistry
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Phytochemical characterization and biological activities of green tea (Camellia sinensis) produced in the Azores, Portugal

2021

Abstract Background Green tea is not only one of the most widely consumed beverages worldwide, but is also known for its health promoting and therapeutic effects. Green tea is cultivated in areas with high humidity and acidic soils in China, Indonesia and Japan. Those places have well-marked dry and rainy seasons. In opposite, Azores have a climate with constant average annual rainfall and, unlike eastern regions, relatively constant air humidity throughout the year. While a brand implemented on the Portuguese market, the quality of green tea produced in Azores must be guaranteed. Quality control measures based on phytochemical determination of the chemical composition and biological activi…

PhytochemistryChemistryDPPHTheaceaeFunctional foodGeneral EngineeringEpigallocatechin gallateTheanineNatural productchemistry.chemical_compoundOther systems of medicineEpicatechin gallatePhytochemicalMaceration (wine)General Earth and Planetary SciencesCamellia sinensisFood scienceGallic acidAntioxidantRZ201-999General Environmental ScienceCancer
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PLA2-mediated catalytic activation of its inhibitor 25-acetyl-petrosaspongiolide M: serendipitous identification of a new PLA2 suicide inhibitor.

2004

Abstract25-Acetyl-petrosaspongiolide M (PMAc) (1), a mild non-covalent PLA2 inhibitor, unexpectedly recovers, after incubation with bvPLA2, the ability to covalently modify the enzyme target. This study demonstrates the catalytic effect of bvPLA2 in converting 1 in its deacetylated congener petrosaspongiolide M (PM) (2), a strong covalent PLA2 inhibitor whose molecular mechanism of inhibition has already been clarified. Moreover, our findings outline the potential role of PMAc as anti-inflammatory pro-drug, by virtue of its ability of delivering the active PM agent at the site of inflammation, functioning as a suicide inhibitor.

Protein ConformationMarine natural productLigandsBiochemistryMass SpectrometryProtein Structure SecondaryCIRCULAR-DICHROISMchemistry.chemical_compoundProtein structureStructural BiologyBINDINGEnzyme InhibitorsChromatography High Pressure Liquidchemistry.chemical_classificationbiologyMolecular StructureChemistryCircular DichroismHydrolysisTemperatureAcetylationHydrogen-Ion ConcentrationBEE VENOM PHOSPHOLIPASE-A2PoriferaPETROSASPONGIOLIDES M-RBiochemistryCovalent bondINACTIVATIONMANOALIDESpectrometry Mass Electrospray IonizationCYTOSOLIC PHOSPHOLIPASE A(2); BEE VENOM PHOSPHOLIPASE-A2; FLUORESCENCE DISPLACEMENT ASSAY; PETROSASPONGIOLIDES M-R; CIRCULAR-DICHROISM; NATURAL-PRODUCTS; INACTIVATION; MANOALIDE; POTENT; BINDINGStereochemistryBiophysicsGroup II Phospholipases A2CatalysisPhospholipases AAnti-inflammatory compoundManoalidePhospholipase A2NATURAL-PRODUCTSGeneticsTrifluoroacetic acidAnimalsBinding siteOleanolic AcidMolecular BiologyBinding SitesPOTENTCYTOSOLIC PHOSPHOLIPASE A(2)Cell BiologyMolecular WeightKineticsPhospholipases A2EnzymeAcetylationbiology.proteinFLUORESCENCE DISPLACEMENT ASSAYPhospholipase A2 inhibitionFEBS letters
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Antioxidant Bibenzyl Derivatives from Notholaena nivea Desv.

2011

Four new bibenzyl derivatives were isolated, together with other known bibenzyls, by bioassay-guided fractionation of a CHCl3-MeOH extract of Notholaena nivea Desv. (Pteridaceae) aerial parts. The structures were elucidated by NMR, ESIMS and other spectral analyses. Their antioxidative effects towards superoxide, lipidic peroxidation and the 2,2'- azino-bis-3- ethilbenzothiazoline-6-sulfonic acid (ABTS) radical were assayed. Results showed that the compound 3,12-dihydroxy-5-methoxybibenzyl (6) is the most active compound in the ABTS free-radical scavenging test, while in the coupled oxidation of ȕ-carotene and linoleic acid assay the compound 5,12-dihydroxy-3-methoxydibenzyl-6- carboxylic a…

PteridaceaeSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyAntioxidantStereochemistrymedicine.medical_treatmentLinoleic acidNatural products active principles oxidative stress.Pharmaceutical ScienceArticleAntioxidantsAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoverymedicineBibenzylPhysical and Theoretical Chemistrychemistry.chemical_classificationABTSbiologyPlant Extractsbibenzyl derivativesSuperoxideOrganic ChemistryNotholaenabiology.organism_classificationNMR<em>Notholaena nivea</em>; bibenzyl derivatives; NMR; antioxidants activityEnzymechemistryBiochemistryChemistry (miscellaneous)PteridaceaeMolecular MedicineNotholaena niveaantioxidants activityMolecules
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Development of a high performance thin layer chromatography method for the rapid qualification and quantification of phenolic compounds and abscisic …

2019

Honey is a natural product with a complex chemical composition consisting of sugars and other bioactive compounds. It is important in many traditional systems of medicine, exhibiting interesting bioactivities, in particular antimicrobial, anti-inflammatory and antioxidant effects. Authentication of botanical origin of honeys is particularly important in this context. Therefore, methods for quality control of honey and detection of its adulteration are very important. A HPTLC method for the quantitative determination of phenolic compounds in honey was developed for the first time. Seven phenolic compounds were detected and determined quantitatively in lime and acacia honey samples. The obtai…

Quality ControlAuthentication of monofloral honeysanimal structuresAcaciaContext (language use)engineering.material010402 general chemistry01 natural sciencesBiochemistryAntioxidantsAnalytical Chemistrychemistry.chemical_compoundPhenolsHigh performance thin layer chromatographyAbscisic acidLimeNatural productChromatographybiologyChromatographic fingerprintsOptimization of chromatographic conditionsHigh-performance thin-layer chromatographydigestive oral and skin physiologyfungi010401 analytical chemistryOrganic Chemistryfood and beveragesHoneyGeneral MedicineAntimicrobialbiology.organism_classificationPhenolic compoundsThin-layer chromatography0104 chemical scienceschemistrybehavior and behavior mechanismsengineeringChromatography Thin LayerFood AnalysisAbscisic AcidJournal of Chromatography A
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Perthamides C-F, potent human antipsoriatic cyclopeptides

2011

Abstract Two new cyclopeptides, perthamides E and F were isolated from the polar extracts of the sponge Theonella swinhoei . The new structures, featuring an unprecedented β-amino acid unit (AHMOA), were determined by interpretation of NMR and MS data. The absolute configuration of the AHMOA residue was proposed on the basis of quantum chemical calculation of NMR chemical shifts. Perthamides were proved to inhibit TNF-α and IL-8 release in primary human keratinocytes cells and therefore could represent potentially leads for the treatment of psoriasis.

Quantum chemicalchemistry.chemical_classificationTheonella swinhoeiStereochemistryChemical shiftOrganic ChemistryAbsolute configurationTheonella swinhoeicyclopeptidesBiochemistryCombinatorial chemistryCyclic peptideResidue (chemistry)Anti-Inflammatory activitychemistryinflammationDrug DiscoveryMarine compoundsCyclic peptidesmarine natural product
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Anodic Oxidation as an Enabling Tool for the Synthesis of Natural Products

2020

Electrochemistry provides a valuable toolbox for organic synthesis and offers an appealing, environmentally benign alternative to the use of stoichiometric quantities of chemical oxidants or reductants. Its potential to control current efficiency along with providing alternative reaction conditions in a classical sense makes electrochemistry a suitable method for large-scale industrial transformations as well as for laboratory applications in the synthesis of complex molecular architectures. Even though research in this field has intensified over the recent decades, many synthetic chemists still hesitate to add electroorganic reactions to their standard repertoire, and hence, the full poten…

Reaction conditionschemistry.chemical_compoundNatural productchemistryAnodic oxidationOrganic ChemistryNanotechnologyOrganic synthesisBond formationElectrochemistryCatalysisSynthesis
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