Search results for "bark"

showing 10 items of 137 documents

Chemical constituents from leaves and root bark of Trichilia monadelpha (Meliaceae)

2018

Abstract Two new limonoid derivatives designated, monadelphin A (1) and monadelphin B (2) and two new sesquiterpene derivatives named trichins A (3) and B (4) were isolated together with six known compounds (5–10) from the mixture of methylene chloride/methanol (1:1) extract of leaves and root bark of Trichilia monadelpha (Meliaceae) collected in Cameroon. The structures of the new compounds were unambiguously established by detailed spectroscopic analysis including 1D and 2D NMR data in conjunction with high resolution mass spectrometry data and by comparison of these data with those of related compounds described in the literature. Compounds 1–4 were screened for their cytotoxic potential…

Meliaceaebiology010405 organic chemistryStereochemistryPlant ScienceSesquiterpenebiology.organism_classificationLimonoidTrichilia monadelpha01 natural sciencesBiochemistryChloride0104 chemical sciences010404 medicinal & biomolecular chemistrychemistry.chemical_compoundchemistryvisual_artmedicinevisual_art.visual_art_mediumBarkMethyleneAgronomy and Crop ScienceTwo-dimensional nuclear magnetic resonance spectroscopyBiotechnologymedicine.drugPhytochemistry Letters
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Styryl-pyrones from Goniothalamus arvensis

1998

Two novel styrl-pyrones, (+)-garvensintriol and (+)-etharvendiol, together with a known cytotoxic furano-furone, (+)-goniofufurone, have been isolated from the stem bark of Goniothalamus arvensis. A different relative configuration, cis-erythro-erythro for garvensintriol and cis-threo-erythro for etharvendiol, is established, and their absolute stereochemistry is discussed.

Models MolecularStem barkMagnetic Resonance SpectroscopyEtharvendiolMolecular StructurebiologyStereochemistryChemistryGarvensintriolPlant ScienceGeneral MedicinePlantsHorticulturebiology.organism_classificationBiochemistryMass SpectrometryPyronesAnnonaceaevisual_artvisual_art.visual_art_mediumBarkMolecular BiologyGoniothalamusPhytochemistry
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3-acetylaltholactone and related styryl-lactones, mitochondrial respiratory chain inhibitors.

2000

A novel furano-pyrone, 3-acetylaltholactone, and two other known styryl-lactones, altholactone and 5-acetoxyisogoniothalamin oxide, have been isolated from Goniothalamus arvensis (Annonaceae) stem bark. We report here the isolation and structural elucidation of these compounds with furane-pyrone and styryl-pyrone skeletons, postulating also for the first time their mechanism of cytotoxicity based on inhibition on mammalian mitochondrial respiratory chain.

Models MolecularStereochemistryChemical structureSubmitochondrial ParticlesMolecular ConformationPlant ScienceHorticultureBiochemistryMitochondria HeartStyrenesLactonesOxygen ConsumptionAnimals3-acetylaltholactoneCytotoxicityFuransMolecular BiologyGoniothalamusStem barkPlants MedicinalbiologyMolecular StructurePlant StemsUncoupling AgentsGeneral Medicinebiology.organism_classificationNADKineticsMitochondrial respiratory chainAnnonaceaePyronesvisual_artvisual_art.visual_art_mediumBarkCattlePhytochemistry
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Polyphasic identification of yeasts isolated from bark of cork oak during the manufacturing process of cork stoppers.

2003

A two-step protocol was used for the identification of 52 yeasts isolated from bark of cork oak at initial stages of the manufacturing process of cork stoppers. The first step in the identification was the separation of the isolates into groups by their physiological properties and RFLPs of the ITS-5.8S rRNA gene. The second step was the sequencing of the D1/D2 domains of the 26S rRNA gene of selected isolates representing the different groups. The results revealed a predominance of basidiomycetous yeasts (11 species), while only two species represented the ascomycetous yeasts. Among the basidiomycetous yeasts, members representing the species Rhodosporidium kratochvilovae and Rhodotorula n…

MycologyCorkengineering.materialRhodotorulaApplied Microbiology and BiotechnologyMicrobiologyDNA RibosomalPolymerase Chain ReactionRhodotorula mucilaginosaQuercusYeastsDebaryomyces hanseniiBotanyTrichosporon mucoidesDNA FungalMycological Typing TechniquesRibosomal DNAbiologyBase SequenceFungal geneticsGeneral Medicinebiology.organism_classificationPhenotypevisual_artvisual_art.visual_art_mediumengineeringPlant BarkBarkPolymorphism Restriction Fragment LengthFEMS yeast research
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Höchstgerichtsbarkeit in den südlichen Niederlanden (16./17. Jahrhundert) : Nicolas du Fief und die Praxis des Grossen und des Geheimen Rates

2008

Nicolas du fief[SHS.DROIT]Humanities and Social Sciences/Law[SHS.DROIT] Humanities and Social Sciences/Law[ SHS.DROIT ] Humanities and Social Sciences/Lawsüdlichen NiederlandenHöchstgerichtsbarkeit
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First measurement of e+e−→pKS0n¯K−+c.c. above open charm threshold

2018

The process e(+)e(-) -> pK(S)(0)(n) over barK(-) + c.c. and its intermediate processes are studied for the first time, using data samples collected with the BESIII detector at BEPCII at center-o ...

Nuclear physicsPhysics010308 nuclear & particles physicsvisual_artElectron–positron annihilation0103 physical sciencesvisual_art.visual_art_mediumBarkOpen charmBorn approximation010306 general physics01 natural sciencesPhysical Review D
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Cytotoxicity of isoflavones and biflavonoids from Ormocarpum kirkii towards multi-factorial drug resistant cancer.

2019

Abstract Background While incidences of cancer are continuously increasing, drug resistance of malignant cells is observed towards almost all pharmaceuticals. Several isoflavonoids and flavonoids are known for their cytotoxicity towards various cancer cells. Purpose The aim of this study was to determine the cytotoxicity of isoflavones: osajin (1), 5,7-dihydroxy-4ˈ-methoxy-6,8-diprenylisoflavone (2) and biflavonoids: chamaejasmin (3), 7,7″-di-O-methylchamaejasmin (4) and campylospermone A (5), a dimeric chromene [diphysin(6)] and an ester of ferullic acid with long alkyl chain [erythrinasinate (7)] isolated from the stem bark and roots of the Kenyan medicinal plant, Ormocarpum kirkii. The m…

Pharmaceutical ScienceApoptosisPlant Roots03 medical and health scienceschemistry.chemical_compound0302 clinical medicineCell Line TumorDrug DiscoveryCytotoxic T cellBiflavonoidsHumansddc:610Cytotoxicity030304 developmental biologyPharmacologychemistry.chemical_classificationMembrane Potential Mitochondrial0303 health sciencesBiflavonoidsPlants MedicinalPlant ExtractsCell CycleBiflavonoidFabaceaeIsoflavonesMolecular biologyAntineoplastic Agents PhytogenicIsoflavonesKenyaDrug Resistance MultipleComplementary and alternative medicinechemistryCell cultureApoptosisDrug Resistance Neoplasm030220 oncology & carcinogenesisCaspasesCancer cellPlant BarkMolecular MedicineInstitut für ChemieReactive Oxygen SpeciesPhytomedicine : international journal of phytotherapy and phytopharmacology
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2019

Phytochemical investigations of ethanol root bark and stem bark extracts of Cleistochlamys kirkii (Benth.) Oliv. (Annonaceae) yielded a new benzopyranyl cadinane-type sesquiterpene (cleistonol, 1) alongside 12 known compounds (2–13). The structures of the isolated compounds were established from NMR spectroscopic and mass spectrometric analyses. Structures of compounds 5 and 10 were further confirmed by single crystal X-ray crystallographic analyses, which also established their absolute stereochemical configuration. The ethanolic crude extract of C. kirkii root bark gave 72% inhibition against the chloroquine-sensitive 3D7-strain malaria parasite Plasmodium falciparum at 0.01 μg/mL. The is…

Pharmaceutical ScienceSesquiterpene01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryCytotoxic T cellPhysical and Theoretical ChemistryCytotoxicityIC50biologyTraditional medicine010405 organic chemistryOrganic ChemistryPlasmodium falciparumbiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryPhytochemicalChemistry (miscellaneous)Annonaceaevisual_artvisual_art.visual_art_mediumMolecular MedicineBarkMolecules
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COX-2 and sPLA2 inhibitory activity of aqueous extract and polyphenols of Rhizophora mangle (red mangrove)

2006

The aqueous extract of Rhizophora mangle bark and its polyphenolic fractions showed remarkable in vitro antiinflammatory activity in a preliminary study. The low molecular weight fraction exhibited cyclooxygenase-2 inhibitory activity while the total aqueous extract and the low molecular weight fraction showed secretory phospholipase A(2) inhibitory activity.

PharmacognosyPhospholipases Alaw.inventionchemistry.chemical_compoundPhenolslawDrug DiscoveryPlant BarkHumansPhenolsEnzyme InhibitorsRhizophora mangleFlavonoidsPharmacologyCyclooxygenase 2 InhibitorsDose-Response Relationship DrugTraditional medicinebiologyPlant ExtractsChemistryMembrane ProteinsPolyphenolsRhizophoraceaeGeneral Medicinebiology.organism_classificationCyclooxygenase 2Polyphenolvisual_artPlant Barkvisual_art.visual_art_mediumRhizophoraceaeBarkPhytotherapyPhytotherapyFitoterapia
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Steroidal saponins from Dracaena marginata

2013

Three new steroidal saponins and ten known ones were isolated from the bark of Dracaena marginata, along with two known steroidal saponins from the roots. Their structures were elucidated on the basis of extensive 1D and 2D NMR experiments and mass spectrometry as (25R)-26-(beta-D-glucopyranosyloxy)3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 --> 2)-[alpha-L-rhamnopyranosyl-(1 --> 4)]-beta-D-glucopyranoside (1), (25R)-26-(beta-D-glucopyranosyloxy)-3beta,22alpha-dihydroxyfurost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 --> 2)-4-O-sulfo-alpha-L-arabinopyranoside (2), and (25S)-3beta-hydroxyspirost-5-en-1beta-yl O-alpha-L-rhamnopyranosyl-(1 --> 2)-4-O-sulfo-alpha-L…

PharmacologyMagnetic Resonance SpectroscopyTraditional medicinebiologyChemistryDracaena marginataPlant ScienceGeneral MedicineNuclear magnetic resonance spectroscopySaponinsMass spectrometrybiology.organism_classificationMiceAsparagaceaeComplementary and alternative medicinevisual_artCell Line TumorDrug Discoveryvisual_art.visual_art_mediumAnimalsHumansBarkTwo-dimensional nuclear magnetic resonance spectroscopyDracaenaDracaena
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