Search results for "Hydrocotyle"

showing 5 items of 5 documents

Light Conditions Affect NaCl-Induced Physiological Responses in a Clonal Plant Species Hydrocotyle vulgaris

2020

Abstract In order to understand if differences in light conditions can affect responses of a clonal plant species to increased soil salinity, the long-term effect of two substrate concentrations of NaCl on leaf growth, clonal plasticity and oxidative enzyme (peroxidase and polyphenol oxidase) activity in Hydrocotyle vulgaris L. plants grown at low, moderate and high light conditions was studied. H. vulgaris appeared to be a shade-tolerant species, since both leaf blade and petiole growth was inhibited at low light intensity. At low light intensity, H. vulgaris plants represented characteristics of halophytes with significant stimulation of leaf blade and petiole growth by NaCl, especially a…

0106 biological sciencesMultidisciplinarybiologyGeneral interestSciencefungiQfood and beveragesoxidative enzymesperoxidasebiology.organism_classificationAffect (psychology)010603 evolutionary biology01 natural sciencesclonal growthPhysiological responsessalinitycoastal habitatsBotanyPlant speciesHydrocotylepolyphenol oxidase010606 plant biology & botanyProceedings of the Latvian Academy of Sciences. Section B, Natural Sciences
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Physiological Performance of a Coastal Marsh Plant Hydrocotyle vulgaris in Natural Conditions in Relation to Mineral Nutrition and Mycorrhizal Symbio…

2020

Abstract Fluctuating soil salinity and competition for light are the main factors affecting plant distribution and performance in coastal salt marshes. The aim of the present study was to assess plant performance by means of non-destructive instrumental methods in a highly heterogeneous natural habitat. More specifically, environmental factors affecting growth and physiological performance of a clonal plant Hydrocotyle vulgaris L. were investigated. Changes in soil salinity, soil mineral characteristics, leaf nutrient concentrations, morphological parameters, chlorophyll fluorescence, and mycorrhizal symbiosis were analysed in different experimental plots of naturally growing H. vulgaris pl…

0106 biological sciencesgeographyMultidisciplinaryMarshgeography.geographical_feature_categorybiologynatural conditionsgrowthScienceQ04 agricultural and veterinary sciencesbiology.organism_classificationchlorophyll a fluorescence040401 food science01 natural sciencesNatural (archaeology)salinity0404 agricultural biotechnologySymbiosisBotanyHydrocotylechlorophyll010606 plant biology & botanyphotosynthetic performanceProceedings of the Latvian Academy of Sciences. Section B, Natural Sciences
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Two New Oleanane-type Saponins from Hydrocotyle multifida

2018

A phytochemical study of a Venezuelan species Hydrocotyle multifida led to the isolation of five oleanane-type glycosides: two previously undescribed and three known ones. Their structures were established by 2D NMR spectroscopic techniques and mass spectrometry as 3- O-β-D-galactopyranosyl-(1→2)-[α-L-arabinopyranosyl-(1→3)]-β-D-glucuronopyranosyloleanolic acid and 3- O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→2)-β-D-glucuronopyrano-syloleanolic acid. These results represent a significative contribution to the chemotaxonomy of the Hydrocotyle genus.

Pharmacologychemistry.chemical_classificationbiologyTraditional medicine010405 organic chemistryChemistryGlycosidePlant ScienceGeneral Medicinebiology.organism_classification01 natural sciences0104 chemical sciences010404 medicinal & biomolecular chemistrychemistry.chemical_compoundType (biology)Complementary and alternative medicinePhytochemicalDrug DiscoveryHydrocotyleAraliaceaeOleananeNatural Product Communications
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Triterpenoid saponins from Hydrocotyle bonariensis Lam

2011

Abstract Phytochemical investigation of the under-ground parts of Hydrocotyle bonariensis led to the isolation of five oleanane-type triterpenoid saponins, 3- O -{β- d -glucopyranosyl-(1 → 2)-[α- l -arabinopyranosyl-(1 → 3)]-β- d -glucuronopyranosyl}-21- O -(2-methylbutyroyl)-22- O -acetyl-R 1 -barrigenol, 3- O -{β- d -glucopyranosyl-(1 → 2)-[α- l -arabinopyranosyl-(1 → 3)]-β- d -glucuronopyranosyl}-21- O -(2-methylbutyroyl)-28- O -acetyl-R 1 -barrigenol, 3- O -{β- d -glucopyranosyl-(1 → 2)-[α- l -arabinopyranosyl-(1 → 3)]-β- d -glucuronopyranosyl}-21- O -acetyl-R 1 -barrigenol, 3- O -{β- d -glucopyranosyl-(1 → 2)-[α- l -arabinopyranosyl-(1 → 3)]-β- d -glucuronopyranosyl}-R 1 -barrigenol, a…

StereochemistryPlant ScienceHorticultureBiochemistryHydrocotyle bonariensisTriterpenoidHumansCameroonNuclear Magnetic Resonance BiomolecularMolecular BiologyMolecular StructurebiologyChemistryStereoisomerismGeneral MedicineSaponinsHCT116 Cellsbiology.organism_classificationAntineoplastic Agents PhytogenicTriterpenesHuman colon cancerDrug Screening Assays AntitumorHT29 CellsTwo-dimensional nuclear magnetic resonance spectroscopyRhizomeApiaceaePhytochemistry
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New Triterpenoid and Ergostane Glycosides from the Leaves of Hydrocotyle umbellata L.

2011

Two new triterpenoid glycosides, together with two new ergostane glycosides, umbellatosides A–D (1–4, resp.), have been isolated from the leaves of Hydrocotyle umbellata L. Their structures were established by 2D-NMR spectroscopic techniques (1H,1H-COSY, TOCSY, NOESY, HSQC, and HMBC) and mass spectrometry as 3β,22β-dihydroxy-3-O-[α-L-rhamnopyranosyl-(12)-β-D-glucuronopyranosyl]olean-12-en-28-oic acid 28-O-β-D-glucopyranosyl ester (1), 3-O-[α-L-rhamnopyranosyl-(12)-β-D-glucuronopyranosyl]oleanolic acid 28-O-β-D-glucopyranosyl ester (2), (3β,11α,26)-ergosta-5,24(28)-diene-3,11,26-triol 3-O-(β-D-glucopyranosyl)-11-O-(α-L-rhamnopyranosyl)-26-O-β-D-glucopyranoside (3), and (3β,11α,21,26)-ergosta…

chemistry.chemical_classificationErgostanebiologyStereochemistryOrganic ChemistryGlycosideHydrocotyle umbellataMass spectrometrybiology.organism_classificationBiochemistryCatalysisInorganic ChemistryTerpenechemistry.chemical_compoundTriterpenoidchemistryDrug DiscoveryOrganic chemistryPhysical and Theoretical ChemistryOleanolic acidTwo-dimensional nuclear magnetic resonance spectroscopyHelvetica Chimica Acta
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