Search results for "Terpenoid"

showing 10 items of 221 documents

New Biologically Active Triterpene-Saponins fromRandia dumetorum

1990

Two new triterpene-saponins, 3-O-[O-beta-D-glucopyranosyl-(1----4)-O-beta-D-glucopyranosyl-(1----3)-( beta- D-glucuronopyranosyl)]oleanolic acid (1), 3-O-[O-beta-D-glucopyranosyl-(1----6)-O-beta-D-glucopyranosyl- (1----3)-(beta-D-glucuronopyranosyl)]oleanolic acid (2) together with five known saponins (3-7) were isolated from the methanolic extract of the fruits of Randia dumetorum (Retz) Lam. (Rubiaceae). Their structures were established on the basis of chemical and spectral data. The compounds 1, 3, 4, 5 were found to enhance significantly the proliferation of human lymphocytes in vitro. The crude saponin fraction showed haemolytic, molluscicidal, and immunostimulating activities.

MolluscacidesStereochemistryRandiaSaponinPharmaceutical SciencePharmacognosyLymphocyte ActivationAnalytical Chemistrychemistry.chemical_compoundTriterpeneDrug DiscoveryAnimalsLymphocytesMedicinal plantsOleanolic acidPharmacologychemistry.chemical_classificationPlants MedicinalRubiaceaeBiomphalariabiologyOrganic ChemistrySaponinsbiology.organism_classificationTriterpenesTerpenoidcarbohydrates (lipids)Complementary and alternative medicinechemistryMolecular MedicinePlanta Medica
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Volatile constituents of the aerial parts of Pulicaria sicula (L.) Moris growing wild in Sicily: Chemotaxonomic volatile markers of the genus Pulicar…

2015

Abstract The chemical composition of the essential oil isolated from the aerial parts of Pulicaria sicula (L.) Moris was characterized by GC-FID and GC/MS analyses. The oil was particularly rich in oxygenated terpenoids. Among the oxygenated monoterpenes (content of 44.5%), the most abundant were borneol (23.7%), bornyl acetate (6.5%), and isothymol isobutyrate (6.2%). Caryophyllene oxide (10.2%), caryophylladienol I (4.3%), and caryophylla-3,8(13)-dien-5β-ol (4.4%) were identified as the main constituents among the oxygenated sesquiterpenes. Furthermore, a complete literature review on the composition of the essential oils of all the Pulicaria taxa studied so far was performed and a princi…

MonoterpenePrincipal-component analysis (PCA)BioengineeringBiochemistryGas Chromatography-Mass SpectrometryEssential oilPulicarialaw.inventionBorneolchemistry.chemical_compoundGenuslawBotanyOils VolatileSettore BIO/15 - Biologia FarmaceuticaSicilyChemical compositionMolecular BiologyEssential oilPrincipal Component AnalysisMolecular StructurebiologyChemistry (all)General ChemistryGeneral MedicinePlant Components Aerialbiology.organism_classificationPulicariaTerpenoidChemotaxonomychemistryPulicaria siculaChemotaxonomyGC/MS AnalysiMolecular MedicineComposition (visual arts)
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Strictosidine—The Biosynthetic Key to Monoterpenoid Indole Alkaloids

1999

Monoterpenoid Indole AlkaloidsStereochemistryChemistryStrictosidineKey (lock)
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New Alkaloids of the Sarpagine Group from Rauvolfia serpentina Hairy Root Culture

2002

Three new monoterpenoid indole alkaloids, 19(S),20(R)-dihydroperaksine (1), 19(S),20(R)-dihydroperaksine-17-al (2), and 10-hydroxy-19(S),20(R)-dihydroperaksine (3), along with 16 known alkaloids 4-19 were isolated from hairy root culture of Rauvolfia serpentina, and their structures were elucidated by 1D and 2D NMR analyses. Taking into account the stereochemistry of the new alkaloids and results of preliminary enzymatical studies, the putative biosynthetical relationships between the novel alkaloids are discussed.

Monoterpenoid Indole AlkaloidsStereochemistryPharmaceutical SciencePharmacognosyPlant RootsRauwolfiaIndole AlkaloidsAnalytical ChemistryRauvolfia serpentinaDrug DiscoveryNuclear Magnetic Resonance BiomolecularPharmacologyFolk medicinePlants MedicinalMolecular StructurebiologyApocynaceaeChemistryAlkaloidOrganic ChemistryStereoisomerismbiology.organism_classificationSecologanin Tryptamine AlkaloidsTerpenoidComplementary and alternative medicineHairy root cultureMolecular MedicineChromatography Thin LayerRhizobiumJournal of Natural Products
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Compositional and morphological analyses of wax in northern wild berry species.

2019

Accepted manuscript version, licensed CC BY-NC-ND 4.0. Aerial surfaces of plants are covered by a waxy cuticle protecting plants from excessive water loss and UV light. In the present study, composition and morphology of cuticular waxes of northern wild berry species bilberry (Vaccinium myrtillus L.), lingonberry (V. vitis-idaea L.), bog bilberry (V. uliginosum L.) and crowberry (Empetrum nigrum L.) were investigated. Scanning electron microscopy (SEM) revealed differences in epicuticular wax morphology, and gas chromatography–mass spectrometry (GC–MS) analysis confirmed variation in chemical composition of cuticular waxes between the berry species. The dominant compounds in bilberry and li…

MorphologyBilberryUltraviolet RaysCuticleBlueberry PlantsChemical compositionVaccinium myrtillusBerryChemical FractionationVaccinium myrtillus01 natural sciencesGas Chromatography-Mass SpectrometryAnalytical ChemistryEpicuticular waxFruitsAnthocyaninsEmpetrum0404 agricultural biotechnologyBotanyVDP::Mathematics and natural science: 400::Zoology and botany: 480Vaccinium vitis-idaeaFinlandWaxbiologyChemistryVDP::Landbruks- og Fiskerifag: 900Plant Extracts010401 analytical chemistryFatty Acids04 agricultural and veterinary sciencesGeneral MedicineTriterpenoidsbiology.organism_classification040401 food science0104 chemical sciencesCuticular waxvisual_artFruitWaxesvisual_art.visual_art_mediumEmpetrum nigrumSun Protection FactorVacciniumFood ScienceVacciniumVDP::Matematikk og Naturvitenskap: 400::Zoologiske og botaniske fag: 480Food chemistry
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The biotransformation of the Diterpenoid, Rosenonolactone by Mucor Plumbeus

2003

The biotransformation of rosenonolactone by the fungus, Mucor plumbeus involves hydroxylation at C-2α C-6β C-12α and epoxidation of the Δ15-alkene.

Mucor plumbeusbiologyChemistryStereochemistryGeneral MedicineGeneral ChemistryFungusbiology.organism_classificationTerpenoidRosenonolactoneTerpeneHydroxylationchemistry.chemical_compoundBiotransformationOrganic chemistryJournal of Chemical Research
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Mycochemicals in wild and cultivated mushrooms: nutrition and health

2021

AbstractThe mushrooms have contributed to the development of active ingredients of fundamental importance in the field of pharmaceutical chemistry as well as of important tools in human and animal health, nutrition, and functional food. This review considers studies on the beneficial effects of medicinal mushrooms on the nutrition and health of humans and farm animals. An overview of the chemical structure and composition of mycochemicals is presented in this review with particular reference to phenolic compounds, triterpenoids and sterols, fatty acids and lipids, polysaccharides, proteins, peptides, and lectins. The nutritional value and chemical composition of wild and cultivated mushroom…

Mycochemical0106 biological sciencesCultivationPlant Science01 natural sciencesFungal diversity Cultivation Mycochemicals Chemical structures Nutrition0404 agricultural biotechnologyNutraceuticalTriterpenoidChemical structureFunctional food010608 biotechnologyFood scienceFungal diversityBeneficial effectsNutritionPleurotusAnimal healthbiologyMycochemicals04 agricultural and veterinary sciencesbiology.organism_classification040401 food scienceChemical structuresnervous systemFungal diversity; Cultivation; Mycochemicals; Chemical structures; NutritionSettore BIO/03 - Botanica Ambientale E Applicatapsychological phenomena and processesBiotechnologyPhytochemistry Reviews
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Neo-clerodane diterpenoids from Teucrium sandrasicum

1997

WOS: A1997XM24100019

Neo-Clerodane DiterpenoidsbiologyStereochemistryPlant ScienceGeneral MedicineLabiataeTeusandrins A-FHorticultureTeucrium Sandiasicumbiology.organism_classificationBiochemistryTeucriumchemistry.chemical_compoundOxetane DerivativeschemistryDiterpeneMolecular BiologyDerivative (chemistry)Phytochemistry
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Diterpenoids from Tetraclinis articulata that Inhibit Various Human Leukocyte Functions

2003

Ten new compounds, eight of them pimarane derivatives (1-8), together with a menthane dimer (9) and a totarane diterpenoid (10), were isolated from the leaves and wood of Tetraclinis articulata. The structures of 1-10 were established by using spectroscopic techniques, including 2D NMR spectra. Pimaranes 1-5 were found to possess an unusual cis interannular union of the B and C rings, which, from a biogenetic perspective, could be derived from the hydration of a carbocation at C-8. Compounds 4-6 and a mixture of 7 and 11 modulated different human leukocyte functions at a concentration of 10 microM, mainly the degranulation process measured as myeloperoxidase release and, to a lesser extent,…

NeutrophilsStereochemistryMonoterpenePharmaceutical ScienceTetraclinisAnalytical Chemistryboatschemistry.chemical_compoundboats.ship_classDrug DiscoveryLeukocytesArticulataHumansPhenolsNuclear Magnetic Resonance BiomolecularPeroxidasePharmacologyPlants MedicinalMolecular StructurePancreatic ElastasebiologyChemistryOrganic ChemistryCupressaceaeStereoisomerismBiological activitybiology.organism_classificationWoodTerpenoidPlant LeavesMoroccoComplementary and alternative medicineLuminescent MeasurementsMolecular MedicineDiterpenesDiterpeneTwo-dimensional nuclear magnetic resonance spectroscopyJournal of Natural Products
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Saponins from the Roots of Nylandtia spinosa

2007

From the roots of Nylandtia spinosa, four new triterpene saponins, 3- O-beta- d-glucopyranosylpresenegenin 28- O-beta- d-galactopyranosyl-(1-->4)-[alpha- l-arabinopyranosyl-(1-->3)]-beta- d-xylopyranosyl-(1-->4)-[beta- d-apiofuranosyl-(1-->3)]-alpha- l-rhamnopyranosyl-(1-->2)-beta- d-fucopyranosyl ester ( 1), 3- O-beta- d-glucopyranosylpresenegenin 28- O-beta- d-galactopyranosyl-(1-->4)-[alpha- l-arabinopyranosyl-(1-->3)]-beta- d-xylopyranosyl-(1-->4)-alpha- l-rhamnopyranosyl-(1-->2)-beta- d-fucopyranosyl ester ( 2), 3- O-beta- d-glucopyranosylpresenegenin 28- O-beta- d-apiofuranosyl-(1-->4)-[beta- d-galactopyranosyl-(1-->2)]-beta- d-xylopyranosyl-(1-->4)-alpha- l-rhamnopyranosyl-(1-->2)-be…

Nylandtia spinosaCoumaric AcidsSpermidineStereochemistrySaponinPharmaceutical SciencePharmacognosyPlant RootsAnalytical ChemistryInhibitory Concentration 50TriterpeneDrug DiscoveryHumansNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationPlants MedicinalMolecular StructureChemistryOrganic ChemistryGlycosideTenuifolinSaponinsTriterpenesTerpenoidPolygalaceaeHuman colon cancerComplementary and alternative medicineMolecular MedicineDrug Screening Assays AntitumorJournal of Natural Products
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