0000000000340923

AUTHOR

Marie-aleth Lacaille-dubois

showing 48 related works from this author

Triterpene glycosides from plants for antibody recognition

2016

PharmacologyAutoimmune diseasechemistry.chemical_classificationbiologybusiness.industryMultiple sclerosisOrganic ChemistryPharmaceutical ScienceGlycosidemedicine.diseaseAnalytical ChemistryComplementary and alternative medicineTriterpenechemistryDrug DiscoveryImmunologybiology.proteinmedicineMolecular MedicineAntibodybusinessPlanta Medica
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Effects of the flavonoids extracted from Spergularia purpurea Pers. on arterial blood pressure and renal function in normal and hypertensive rats

2001

The antihypertensive and diuretic effects of the flavonoids extracted from Spergularia purpurea Pers. (SP) were studied both in normotensive (NTR) and spontaneously hypertensive conscious rats (SHR). Daily oral administration of the flavonoid mixture (5 mg/kg for 1 week) exhibited a significant decrease in blood pressure with variation coefficient (Delta) of 20 in SHR rats and 11 in NTR rats. The systolic and diastolic blood pressure decreased significantly and respectively with 17 and 24% in SHR, and with 11 and 16% in NTR. The flavonoid mixture enhanced significantly the water excretion in hypertensive (P<0.001) and normal rats (P<0.001). Furthermore, oral administration of flavonoids mix…

Malemedicine.medical_specialtyUrinary systemmedicine.medical_treatmentAdministration OralRenal functionBlood PressureKidneyKidney Function Testslaw.inventionOral administrationlawRats Inbred SHRInternal medicineDrug DiscoveryHeart ratemedicineAnimalsRats WistarDiureticsAntihypertensive AgentsFlavonoidsPharmacologybiologyPlant Extractsbusiness.industryfood and beveragesbiology.organism_classificationRatsBlood pressureEndocrinologyHypertensionDiureticPhytotherapybusinessSpergulariaJournal of Ethnopharmacology
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Secondary metabolites from polar fractions of Piper umbellatum.

2012

Seven known secondary metabolites were isolated from the methanol extract of the branches of Piper umbellatum. The identification of these compounds was mainly achieved by 2D NMR spectroscopic techniques and FAB-MS. Among them, the known cepharadiones A and B can be considered as chemotaxonomic markers of the genus Piper.

PharmacologyPiperFlavone glycosidesChromatographybiologyChemistryPlant ExtractsPlant ScienceGeneral MedicinePiperaceaebiology.organism_classificationComplementary and alternative medicineDrug DiscoveryPiper umbellatumPiperNatural product communications
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New terpenoid glycosides from Eriocoelum microspermum

2017

chemistry.chemical_classificationchemistryTraditional medicineChemical engineeringbusiness.industryEriocoelum microspermumMedicineGlycosidebusinessTerpenoid65th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA 2017)
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New ursolic and betulinic derivatives as potential cytotoxic agents.

2003

Fifteen new ursolic and betulinic triterpenoids, bearing various functionalities at C-3 and C-28 were synthesized as potential cytotoxic agents. All compounds were obtained by a hemisynthetic route via ursolic and betulinic acids. Preliminary screening of these compounds on human HT 29 colon cancer cells revealed inhibitory activity for three of them. Beta-D-Glucopyranosyl-3beta-hydroxyurs-12(13)-en-28-oate 1c, 3beta-3-(3-pyridyl)-prop-2-enoyloxyurs-12(13)-en-28-oic acid 1i and the potassium salt of 3beta-cinnamoyloxylup-20(29)-en-28-oic acid 2d demonstrated cytotoxic activity in the micromolar range: 8.0, 45.0 and 8.0 microM, respectively.

PharmacologyMolecular StructureStereochemistryCell SurvivalAntineoplastic AgentsGeneral MedicineTriterpeneschemistry.chemical_compoundInhibitory Concentration 50Structure-Activity RelationshipTriterpenoidUrsolic acidchemistryBetulinic acidDrug DiscoveryCytotoxic T cellHumansDrug Screening Assays AntitumorBetulinic AcidCytotoxicityPentacyclic TriterpenesHT29 CellsJournal of enzyme inhibition and medicinal chemistry
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Triterpene Saponins from the Fruits of Phytolacca rugosa (Phytolaccaceae)

2010

Four known serjanic acid glycosides were isolated from the fruits of Phytolacca rugosa and characterized mainly by 2D NMR spectroscopy and mass spectrometry. This aglycon has a chemotaxonomic significance for the genus Phytolacca.

Pharmacologychemistry.chemical_classificationbiologyPlant compositionGlycosidePlant ScienceGeneral MedicinePhytolacca rugosabiology.organism_classificationPhytolaccaceaeComplementary and alternative medicineTriterpenechemistryChemotaxonomyDrug DiscoveryBotanyPhytolaccaNatural Product Communications
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Characterization of the biosynthesis of saponins during seed development in peas (Pisum sativum)

2019

National audience; The use of pulses as ingredients for the production of food products rich in plant proteins is increasing. However, protein fractions prepared from pea or other pulses contain significant amounts of saponins, glycosylated triterpenes which can impart a bitter taste to the final food product. Bitter flavours are currently either removed by energy-requiring physico-chemical treatments or masked by additives. We are in the process of identifying and characterizing the genes involved in saponin biosynthesis during pea seed development, with the objective of identifying mutants in which seed saponins no longer accumulate. To do this we have applied a saponin extraction protoco…

[SDV] Life Sciences [q-bio][SDE] Environmental Sciencescarbohydrates (lipids)[SDV]Life Sciences [q-bio]parasitic diseases[SDE]Environmental Sciencesfood and beverages[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[SDV.BV] Life Sciences [q-bio]/Vegetal Biologyoff-flavourproteincomplex mixturessaponin
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Triterpene Saponins from the Roots of Achyranthes bidentata

2001

Three saponins, oleanolic acid-28- O -s-D-glucopyranoside (1), chikusetsusaponin V (2), and 3- O -s-D-glucopyranosyl-oleanolic acid-28- O -s-D-glucopyranoside (3) were isolated from the roots of Achyranthes bidentata Blume (Amaranthaceae). No activity was shown in the granulocyte phagocytosis test nor in the test of the potentiation of the cytotoxicity of cisplatin in human colon cancer cells. This is the first report of compounds 1, 2 and 3 isolated from Achyranthes species. Furthermore, the NMR data of 2 completed the partially published data.

Pharmacologychemistry.chemical_classificationTraditional medicineSaponinPharmaceutical ScienceBiological activityGeneral MedicineAmaranthaceaeBiologybiology.organism_classificationIn vitroComplementary and alternative medicinechemistryTriterpeneDrug DiscoveryMolecular MedicineAchyranthesCytotoxicityAchyranthes bidentataPharmaceutical Biology
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Grain legumes for human consumption: management of off-flavours

2020

International audience

[SDV] Life Sciences [q-bio]ff-flavoursaponinsTILLING[SDV]Life Sciences [q-bio]peaComputingMilieux_MISCELLANEOUS[SHS]Humanities and Social Sciences
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Antinociceptive Effects of Turkish Endemic Eryngium kotschyi Boiss. Roots by Bioactivity Guided Fractionation

2010

Eryngium species (Apiaceae) are well known plants in ethnobotanical culture throughout world and also in Turkey. They are used as antitussive, diuretic as well as for analgesic and antiinflammatory purposes in traditional medicine. This study aimed to evaluate the antinociceptive activity of endemic Eryngium kotschyi Boiss. root extracts by bioguided fractionation. The antinociceptive activity of the extracts/fractions/compound was studied in mice using acetic acid induced writhing test and and hot plate test. The methanolic extract was sequentially partitioned with hexane, dichloromethane and water saturated n-butanol. Among the fractions, the n-BuOH fraction showed the most significant re…

lcsh:Chemistrylcsh:QD241-441Eryngium kotschyilcsh:QD1-999lcsh:Organic chemistrylcsh:BotanyErdem S. A. ARIHAN O. MITAINE-OFFER A. İSKİT A. B. Kartal M. LACAILLE-DUBOIS M. -Antinociceptive Effects of Turkish Endemic Eryngium kotschyi Boiss. Roots by Bioactivity Guided Fractionation- RECORDS OF NATURAL PRODUCTS cilt.10 ss.168-175 2016fractionationtriterpene saponinantinociceptiveApiaceaelcsh:QK1-989
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Antioxidant effect of Ajuga iva aqueous extract in streptozotocin-induced diabetic rats.

2009

The purpose of this study was to investigate the possible antioxidant effect of an aqueous extract of Ajuga iva (Ai) in streptozotocin (STZ)-induced diabetic rats. Twelve diabetic rats were divided into two groups fed a casein diet supplemented or not with Ai (0.5%), for 4 weeks. In vitro, the Ai extract possessed a very high antioxidant effect (1 mg/ml was similar to those of trolox 300 mmol/l). The results indicated that plasma thiobarbituric acid reactive substances (TBARS) values were reduced by 41% in Ai-treated compared with untreated diabetic rats. TBARS concentrations were lower 1.5-fold in liver, 1.8-fold in heart, 1.9-fold in muscle and 2.1-fold in brain in Ai-treated than untreat…

Blood GlucoseMalemedicine.medical_specialtyAntioxidantThiobarbituric acidmedicine.medical_treatmentGlutathione reductasePharmaceutical ScienceEnzyme-Linked Immunosorbent AssayNitric OxideThiobarbituric Acid Reactive SubstancesAntioxidantsStreptozocinLipid peroxidationchemistry.chemical_compoundInternal medicineDrug DiscoverymedicineTBARSAnimalsInsulinRats WistarPharmacologychemistry.chemical_classificationPlant ExtractsGlutathione peroxidaseBody WeightGlutathioneOrgan SizeCarotenoidsLipidsRatsEndocrinologyComplementary and alternative medicinechemistryBiochemistryMolecular MedicineTroloxLipid PeroxidationPhytomedicine : international journal of phytotherapy and phytopharmacology
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Updated insights into the mechanism of action and clinical profile of the immunoadjuvant QS-21: A review

2019

Background Vaccine adjuvants are compounds that significantly enhance/prolong the immune response to a co-administered antigen. The limitations of the use of aluminium salts that are unable to elicite cell responses against intracellular pathogens such as those causing malaria, tuberculosis, or AIDS, have driven the development of new alternative adjuvants such as QS-21, a triterpene saponin purified from Quillaja saponaria. Purpose The aim of this review is to attempt to clarify the mechanism of action of QS-21 through either receptors or signaling pathways in vitro and in vivo with special emphasis on the co-administration with other immunostimulants in new adjuvant formulations, called a…

InflammasomesT-Lymphocytesmedicine.medical_treatmentHerpes zosterPharmaceutical ScienceMonophosphoryl Lipid AAPCs antigen presenting cellsMiceCMI cell mediated immunity0302 clinical medicineDrug DiscoveryHerpes Zoster VaccineMedicineNSCLC non small cell lung carcinomaCancerImmunity CellularVaccines Synthetic0303 health sciencesImmunogenicityIl-2 interleukine 2HIV human immunodeficiency virusLipid A030220 oncology & carcinogenesisCytokinesMolecular MedicineDCs dendritic cellsNK natural killerAdjuvantTLR Toll-like receptorHerpes Zoster VaccineCD cluster of differentiationAntigen-Presenting CellsCTL cytotoxic T lymphocytesHZ herpes zosterMPL 3-deacylated monophosphoryl lipidVaccine adjuvantImmunoadjuvantArticleVZV varicella zoster virus03 medical and health sciencesImmune systemAdjuvants ImmunologicAntigenPAMPs pathogen-associated molecular patternsMalaria VaccinesPRRs pathogen recognition receptorsQS-21 Quillaja saponaria Molina-fraction 21AnimalsMHC major histocompatibility complexMtb Mycobacterium tuberculosis bacteriaSARS severe acute respiratory syndromeAntigen-presenting cellIFN-γ interferon-gamma030304 developmental biologyPharmacologybusiness.industryA-β amyloid-betaTNF-α tumor necrosis factor-alphaSaponinsQS-21MalariaQuillaja saponariaComplementary and alternative medicineTCR T-cell receptorLiposomesImmunologyKLH keyhole limpet hemocyaninbusinessdLN draining lymph nodesMAPK mitogen activated protein kinasePhytomedicine
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Steroidal saponins and flavan-3-ol glycosides from Dioscorea villosa

2006

chemistry.chemical_classificationchemistrybiologyDioscorea villosaDioscoreaceaeBotanyGlycosideFlavan-3-olbiology.organism_classificationBiochemistryEcology Evolution Behavior and SystematicsBiochemical Systematics and Ecology
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New Steroidal Alkaloids from Solanum Hypomalacophyllum

2010

Two new steroidal alkaloids (1-2) have been isolated from the leaves and roots of Solanum hypomalacophyllum Bitter, respectively. Their structures have been elucidated as deacetoxysolaphyllidine-3- O-β-D-glucopyranoside (1) and 4-keto-5,6-dihydro-(20 S)-verazine (2). Furthermore, two known steroidal alkaloids, 20 R-verazine and 20 S-verazine, and the common secondary metabolites oleanolic acid and β-sitosterol were isolated from the roots, whereas deacetoxysolaphyllidine was obtained from the leaves.

PharmacologybiologyPlant compositionChemical structurePlant ScienceGeneral Medicinebiology.organism_classificationchemistry.chemical_compoundComplementary and alternative medicinechemistryDrug DiscoveryBotanySolanumChemical compositionOleanolic acidSolanaceaeNatural Product Communications
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Effect of an aqueous extract of Ajuga iva on glycaemia, reverse cholesterol transport and atherogenic ratios in rats with streptozotocin-induced diab…

2008

Aqueous extractNutrition and DieteticsbiologyChemistryReverse cholesterol transportMedicine (miscellaneous)Pharmacologymedicine.diseaseStreptozotocinbiology.organism_classificationAjugaDiabetes mellitusmedicinemedicine.drugProceedings of the Nutrition Society
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ChemInform Abstract: Two Triterpene Saponins from Achyranthes bidentata.

2010

Bidentatoside II (1) and chikusetsusaponin V methyl ester (2) are two further triterpene saponins isolated from the roots of Achyranthes bidentata. Chemical and homo and heteronuclear two-dimensional (2D) NMR techniques have led to the structural elucidation of 1 which is a new seco-glycoside of oleanolic acid and the full 1H- and 13C-NMR assignments of 2. These compounds did not show any potentiation of the in vitro cytotoxicity of cisplatin in the HT 29 human colon cancer cell line.

Cisplatinchemistry.chemical_classificationbiologyGeneral Medicinebiology.organism_classificationTerpenechemistry.chemical_compoundchemistryBiochemistryHeteronuclear moleculeTriterpeneCell culturemedicineChikusetsusaponin VOleanolic acidAchyranthes bidentatamedicine.drugChemInform
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ChemInform Abstract: Two New Sesquiterpene Derivatives from the Tunisian Endemic Ferula tunetana Pom.

2010

A new sesquiterpene ester, tunetanin A (1), a new sesquiterpene coumarin, tunetacoumarin A (2), together with eight known compounds, i.e., coladin (3), coladonin (4), isosmarcandin (5), 13-hydroxyfeselol (6), umbelliprenin (7) propiophenone (8), beta-sitosterol (9), and stigmasterol (10), were isolated from the roots of Ferula tunetana. Their structures were elucidated on the basis of extensive spectroscopic methods, including 1D- and 2D-NMR experiments and MS analysis, as well as by comparison with published data. The cytotoxicity of compounds 1-7 towards two human colon cancer cell lines, HT-29 and HCT 116, was evaluated. Compounds 3, 4, and 6 showed weak cytotoxic activities.

Terpenechemistry.chemical_compoundStigmasterolchemistryPropiophenoneStereochemistryFerula tunetanaGeneral MedicineSesquiterpeneCytotoxicityCoumarinUmbellipreninChemInform
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Bioactive saponins from plants: An update

2000

Plant saponins are a group of naturally occuring triterpene or steroid glycosides which include a large number of biologically and pharmacologically active compounds. Saponins have been shown in both in vitroand in vivoexperimental test systems during the last decade to possess a broad spectrum of biological and pharmacological activities. This review will summarize some of the recent advances concerning cancer-related activity, immunostimulating, immunoadjuvant, antihepatotoxic, antiphlogistic, antiallergic, molluscicidal, hemolytic, antifungal, antiviral, and hypoglycemic activities. In addition, the effects on the cardiovascular system and the central nervous system will be discussed tog…

Antifungalchemistry.chemical_classificationBroad spectrumchemistryTriterpenemedicine.drug_classmedicine.medical_treatmentmedicineGlycosidePharmacologyBiologyImmunoadjuvantSteroid
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Effect of aqueous extract of Ajuga iva supplementation on plasma lipid profile and tissue antioxidant status in rats fed a high-cholesterol diet

2006

Abstract The present study was designed to explore the possible antioxidant and hypolipidemic effects of the aqueous extract of Ajuga iva (0.5% in the diet) in rats fed a high-cholesterol (1%) diet (HCD). The results indicated that the HCD-Ai versus HCD treatment led to many changes in biochemical parameters. They showed a decrease of plasma total cholesterol (TC) and VLDL-cholesterol but an increase of HDL2-cholesterol. The triacylglycerol contents were reduced in plasma and in VLDL. The lipid peroxidation determined by TBARS was decreased by 75% in plasma. TBARS in liver, heart and kidneys were highly reduced excepted in the adipose tissue. Ajuga iva treatment enhanced superoxide dismutas…

Malemedicine.medical_specialtyVery low-density lipoproteinAntioxidantLipoproteinsmedicine.medical_treatmentHypercholesterolemiaAdipose tissueAjugaThiobarbituric Acid Reactive SubstancesAntioxidantsAjugaCholesterol DietaryLipid peroxidationEatingchemistry.chemical_compoundInternal medicineDrug DiscoverymedicineTBARSAnimalsRats WistarPharmacologybiologyPlant ExtractsCholesterolBody WeightOrgan Sizebiology.organism_classificationLipidsDietEnzymesRatsEndocrinologychemistryDietary SupplementsIntestinal cholesterol absorptionlipids (amino acids peptides and proteins)Journal of Ethnopharmacology
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Steroidal Saponins from the Fruits of Cestrum ruizteranianum

2011

Seven spirostane and furostane-type glycosides were isolated from the aqueous methanolic extract of the fruits of Cestrum ruizteranianum and characterized mainly by 2D NMR spectroscopy and mass spectrometry. These known saponins belong to the Δ5-spirostene and Δ5-furostene series and are reported in this species for the first time.

Pharmacologychemistry.chemical_classificationChromatographybiologyChemistryCestrumGlycosidePlant ScienceGeneral MedicineNuclear magnetic resonance spectroscopyMass spectrometrybiology.organism_classificationComplementary and alternative medicineDrug DiscoverySpectroscopyTwo-dimensional nuclear magnetic resonance spectroscopyNatural Product Communications
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β-Amyrin Synthase1 Controls the Accumulation of the Major Saponins Present in Pea (Pisum sativum)

2021

Abstract The use of pulses as ingredients for the production of food products rich in plant proteins is increasing. However, protein fractions prepared from pea or other pulses contain significant amounts of saponins, glycosylated triterpenes that can impart an undesirable bitter taste when used as an ingredient in foodstuffs. In this article, we describe the identification and characterization of a gene involved in saponin biosynthesis during pea seed development, by screening mutants obtained from two Pisum sativum TILLING (Targeting Induced Local Lesions IN Genomes) populations in two different genetic backgrounds. The mutations studied are located in a gene designated PsBAS1 (β-amyrin s…

0106 biological sciencesTILLINGPhysiologyMutantNonsense mutationPlant Sciencemedicine.disease_cause01 natural sciencesPisum03 medical and health sciencesSpatio-Temporal AnalysisSativumGene Expression Regulation PlantLoss of Function Mutationmedicine[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyIntramolecular TransferasesGenePlant Proteins030304 developmental biology2. Zero hunger[SDV.EE]Life Sciences [q-bio]/Ecology environment0303 health sciencesMutationbiologyPeasfood and beveragesCell BiologyGeneral MedicineSaponinsbiology.organism_classificationBiochemistrySeedsFunctional genomics010606 plant biology & botany
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ChemInform Abstract: Two New Retigerane-Type Sesterterpenoids from the Lichen Leprocaulon microscopicum.

2016

Two new compounds (I) and (II) are isolated, possessing a rare pentacyclic carbon skeleton typical for lichen metabolism, and quite unusual in the vegetal kingdom.

Terpenestomatognathic diseasesType (biology)ChemistryStereochemistryLeprocaulon microscopicumCarbon skeletonOrganic chemistryGeneral MedicineLichenChemInform
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Constituents isolated from Polyscias fulva

2004

biologyChemotaxonomyBotanyPolyscias fulvaAraliaceaebiology.organism_classificationBiochemistryEcology Evolution Behavior and SystematicsPolysciasBiochemical Systematics and Ecology
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Dracoside, a New Steroidal Saponin fromHelleborus purpurascens

1994

Abstract A new steroidal saponin, 1-O-[6-O-acetyl-β-D-galactopyranosyl]-24-O-[β-D-apiofuranosyl-(1→3)-4-O-acetyl-α-L-rhamnopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-arabinopyranosyl]-dracogenin, was isolated from the roots of Helleborus purpurascens and named dracoside. Structure elucidation was performed by chemical transformations and various spectroscopic methods, mainly 2D NMR techniques (COSY, HMQC, HMBC).

chemistry.chemical_classificationStereochemistryChemistrySaponinMolecular MedicineHelleborus purpurascensTwo-dimensional nuclear magnetic resonance spectroscopyNatural Product Letters
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A new ecdysteroid and other constituents from two Dioscorea species

2008

Phytochemical investigation of the rhizome of Dioscorea dumetorum has led to the isolation by several chromatographic steps on normal and reversed phase silica gel of a new ecdysteroid, (20R)-5β,11α,20-trihydroxyecdysone (1), and two known ecdysteroids, ajugasterone C (2) and herkesterone (3). Their structures were determined by spectroscopic methods including 1D- and 2D-NMR (COSY, TOCSY, HSQC and HMBC). This is the first report on the occurrence of phytoecdysteroids in the Dioscoreaceae family. These compounds were devoid of antifungal activity against three Candida species (Candida albicans, Candida glabrata and Candida tropicalis, MIC > 200 μg/ml).

Dioscoreaceae01 natural sciencesBiochemistryCandida tropicalischemistry.chemical_compoundDioscoreaceaeCandida albicansDioscorea schimperianaDioscorea dumetorumEcology Evolution Behavior and SystematicsEcdysteroidChromatographybiologyCandida glabrata010405 organic chemistryEcdysteroidsbiology.organism_classification0104 chemical sciences3. Good healthRhizome010404 medicinal & biomolecular chemistrychemistryPhytochemicalBiochemistry[SDV.SP.PHARMA]Life Sciences [q-bio]/Pharmaceutical sciences/PharmacologyDioscorea2D-NMR
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Triterpene Saponins from Wisteria floribunda “macrobotrys” and “rosea”

2017

Five oleanane-type saponins were isolated from two cultivars of Wisteria floribunda (Willd.) DC. (Fabaceae): From the roots of Wisteria floribunda “macrobotrys”, one new oleanane derivative elucidated as 3- O-β-D-xylopyranosyl-(1→2)-β-D-glucuronopyranosyl-22- O-acetyl-3p,22p,24-trihydroxyolean-12-en-30-oic acid, and two known glycosides, and from the roots of Wisteria floribunda “rosea”, two known ones. Their structures were elucidated by a detailed 600 MHz NMR analysis including 1D and 2D NMR (1H, 13C, COSY, TOCSY, ROESY, HSQC, HMBC) experiments and mass spectrometry. Chemotaxonomic conclusions were proposed.

Pharmacologychemistry.chemical_classificationTraditional medicinebiology010405 organic chemistryPlant ScienceGeneral MedicineFabaceaeWisteria floribundabiology.organism_classification01 natural sciences0104 chemical sciences010404 medicinal & biomolecular chemistrychemistry.chemical_compoundPlant scienceComplementary and alternative medicinechemistryTriterpeneDrug DiscoveryOleananeDerivative (chemistry)Natural Product Communications
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Supporting information - Supplemental material for Triterpenoid Saponins From the Stem Bark of Pentaclethra eetveldeana

2019

Supplemental material, Supporting information for Triterpenoid Saponins From the Stem Bark of Pentaclethra eetveldeana by David Pertuit, Mpuza Kapundu, Anne-Claire Mitaine-Offer, Tomofumi Miyamoto, Chiaki Tanaka, Clément Delaude, and Marie-Aleth Lacaille-Dubois in Natural Product Communications

FOS: Clinical medicine111599 Pharmacology and Pharmaceutical Sciences not elsewhere classified
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Cytotoxic glycosides from the roots of Weigela x “Bristol Ruby”

2019

International audience; Seven oleanane-type glycosides were extracted and isolated by various chromatographic methods from the roots of Weigela x "Bristol Ruby" (1-7), six previously undescribed (1-6) and a known one (7). Their structures were assigned by spectroscopic analysis mainly 2D NMR and mass spectrometry (ESIMS). Selected triterpenoid glycosides (1-3, 6, 7) displayed a good cytotoxic activity against a mouse colon cancer cell line CT26.

WeigelaCytotoxicityPhytochemicalsOleanolic acid glycosidesMass spectrometryPlant Roots01 natural sciencesCaprifoliaceaeMiceTriterpenoidCell Line TumorDrug Discovery[SDV.IDA]Life Sciences [q-bio]/Food engineeringAnimalsCytotoxic T cellGlycosidesOleanolic AcidCytotoxicityCaprifoliaceaePharmacologychemistry.chemical_classificationChromatographyMolecular Structurebiology010405 organic chemistryGlycosideGeneral MedicineWeigela x “Bristol Ruby”biology.organism_classificationAntineoplastic Agents PhytogenicTriterpenesNMR3. Good health0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryTwo-dimensional nuclear magnetic resonance spectroscopy
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Steroidal saponins from the aerial parts of Cordyline fruticosa L. var. strawberries.

2019

A new sulfated steroidal derivative (fruticogenin A: 1-sulfo-australigenin-3-sodium sulphate, 1) and three new steroidal saponins named fruticoside K (3-sulfo-spirostan-25(27)-ene-1β,3β-diol-1-O-[α-L-rhamnopyranosyl-(1 → 4)-β-D-fucopyranoside], 2), fruticoside L (3-sulfo-spirostan-25(27)-ene-1β,3β,6α-triol-1-O-[α-L-rhamnopyranosyl-(1 → 4)-β-D-fucopyranoside], 3) and fruticoside M (spirostan-25(27)-ene-1β,3α-diol-1-O-[α-L-rhamnopyranosyl-(1 → 2)-α-L-rhamnopyranoside], 4) were isolated from the aerial parts of Cordyline fruticosa L. var. strawberries. Their structures were established on the basis of 1D and 2D NMR data, mass spectrometry and chemical methods. Compounds 2 and 4 exhibited weak …

Cordyline fruticosaCordylineStereochemistryPhytochemicalsBreast AdenocarcinomaMass spectrometrychemistry.chemical_compoundSulfationColon carcinomaCell Line TumorDrug DiscoveryHumansCameroonCytotoxicityPharmacologybiologyMolecular StructurePhytosterolsGeneral MedicinePlant Components AerialSaponinsbiology.organism_classificationAntineoplastic Agents PhytogenicchemistryTwo-dimensional nuclear magnetic resonance spectroscopyDerivative (chemistry)Fitoterapia
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Antinociceptive and anti-inflammatory activities of Acacia pennata wild (Mimosaceae)

2005

The butanolic fraction of dried leaves of Acacia pennata (Mimosaceae) was tested for analgesic and anti-inflammatory activities in animal models. It showed significant protective effects against chemical stimuli (acetic acid and formalin) in the mouse. It also produced a significant increase of the threshold of sensitivity to pressure-induced pain in the rats. The extract revealed an inhibitory effect in carrageenin-induced rat paw oedema in the late phase. The results suggested that a peripheral mechanism is involved in the analgesic, associated to anti-inflammatory effect (NSAIDs-like). Among the class of compounds characterized in this fraction, flavonoids may be mainly responsible for t…

MaleMimosamedicine.drug_classButanolsAnalgesicDrug Evaluation PreclinicalAdministration OralPainAcacia pennataAcaciaPharmacognosyCarrageenanAnti-inflammatoryMiceAcetic acidchemistry.chemical_compoundFormaldehydeDrug DiscoveryPressuremedicineAnimalsEdemaRats WistarTramadol5-HT receptorAcetic AcidFlavonoidsPharmacologyDose-Response Relationship DrugbiologyTraditional medicinePlant ExtractsAnti-Inflammatory Agents Non-SteroidalAnalgesics Non-Narcoticbiology.organism_classificationStimulation ChemicalHindlimbRatsPlant LeavesDisease Models AnimalNociceptionchemistryFemaleJournal of Ethnopharmacology
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Changes in antioxidant defense status in hypercholesterolemic rats treated with Ajuga iva.

2007

Abstract The aim of the study was to investigate the effect of aqueous extract of Ajuga iva ( Ai ) on serum and tissues lipid peroxidation as well as antioxidant enzymes activities in red blood cells (RBC) and tissues, in high hypercholesterolemic rats (HC). Male Wistar rats ( n =12) were fed on 1% cholesterol-enriched diet for 15 d. After this adaptation phase, hypercholesterolemic rats (total cholesterol=6.5±0.6 mol/l) were divided into two groups fed the same diet and treated or not with Ai for 15 d. Thiobarbituric acid reactive substances (TBARS) concentrations in serum, LDL-HDL 1 , HDL 2 and HDL 3 were respectively, 5-, 7.8-, 2.3- and 5-fold lower in Ai treated than untreated hyperchol…

Malemedicine.medical_specialtyAntioxidantErythrocytesThiobarbituric acidmedicine.medical_treatmentGlutathione reductaseHypercholesterolemiaPharmaceutical ScienceAdipose tissueAjugaNitric OxideAjugaAntioxidantsLipid peroxidationCholesterol Dietarychemistry.chemical_compoundEatingInternal medicineDrug DiscoverymedicineTBARSAnimalsRats WistarPharmacologychemistry.chemical_classificationbiologyPlant ExtractsGlutathione peroxidaseBody WeightVitaminsbiology.organism_classificationGlutathioneRatsEndocrinologyCholesterolComplementary and alternative medicinechemistryBiochemistryMolecular MedicineLipid PeroxidationPhytotherapyPhytomedicine : international journal of phytotherapy and phytopharmacology
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A review of the biological and pharmacological activities of saponins.

1996

Summary This paper reviews the important biological and pharmacological activities of saponins reported over the last few years. These include cancer-related activity, as well as antiphlogistic and antiallergic, immunomodulating, antihepatotoxic, antiviral, hypoglycemic, antifungal and molluscicidal activities. The action of saponins on the cardiovascular, central nervous, and endocrine systems and other miscellaneous effects are also discussed.

carbohydrates (lipids)PharmacologyAntifungalTriterpenoidComplementary and alternative medicinemedicine.drug_classDrug DiscoverymedicinePharmaceutical ScienceMolecular MedicineBiological activityBiologyPharmacologyPhytomedicine : international journal of phytotherapy and phytopharmacology
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Portulaca oleracea reduces triglyceridemia, cholesterolemia, and improves lecithin: cholesterol acyltransferase activity in rats fed enriched-cholest…

2014

Abstract Purpose The effects of Portulaca oleracea ( Po ) lyophilized aqueous extract were determined on the serum high-density lipoproteins (HDL 2 and HDL 3 ) amounts and composition, as well as on lecithin: cholesterol acyltansferase (LCAT) activity. Methods Male Wistar rats ( n  = 12) were fed on 1% cholesterol-enriched diet for 10 days. After this phase, hypercholesterolemic rats (HC) were divided into two groups fed the same diet supplemented or not with Portulaca oleracea ( Po -HC) (0.5%) for four weeks. Results Serum total cholesterol (TC) and triacylglycerols (TG), and liver TG values were respectively 1.6-, 1.8-, and 1.6-fold lower in Po -HC than in HC group. Cholesterol concentrat…

Malemedicine.medical_specialtyfood.ingredientHypercholesterolemiaPharmaceutical SciencePortulacaPortulacaLecithinCholesterol DietaryPhosphatidylcholine-Sterol O-Acyltransferasechemistry.chemical_compoundfoodInternal medicineDrug DiscoverymedicineAnimalsRats WistarTriglyceridesHypolipidemic AgentsPharmacologychemistry.chemical_classificationHypertriglyceridemiaChromatographybiologyCholesterolPlant ExtractsReverse cholesterol transportbiology.organism_classificationPlant LeavesEnzymeEndocrinologyCholesterolComplementary and alternative medicinechemistryLiverLecithin—cholesterol acyltransferasebiology.proteinMolecular Medicinelipids (amino acids peptides and proteins)Composition (visual arts)Acyl groupPhytomedicine : international journal of phytotherapy and phytopharmacology
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Beneficial effects of a methanolic extract of Globularia alypum on glycaemia, lipid peroxidation and antioxidant enzymes activities in rats with stre…

2008

chemistry.chemical_classificationAntioxidantNutrition and Dieteticsmedicine.medical_treatmentMedicine (miscellaneous)PharmacologyStreptozotocinmedicine.diseaseGlobularia alypumLipid peroxidationchemistry.chemical_compoundEnzymeBiochemistrychemistryDiabetes mellitusmedicineBeneficial effectsmedicine.drugProceedings of the Nutrition Society
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Activation of a Sweet Taste Receptor by Oleanane-Type Glycosides from Wisteria sinensis

2022

The phytochemical study of Wisteria sinensis (Sims) DC. (Fabaceae), commonly known as the Chinese Wisteria, led to the isolation of seven oleanane-type glycosides from an aqueous-ethanolic extract of the roots. After successive purifications by various chromatographic methods, like solid/liquid chromatographic methods, vacuum liquid chromatography (VLC), medium pressure liquid chromatography (MPLC), on normal and reverse phase (RP-18 silica gel), and size exclusion chromatography on Sephadex L, their structures were elucidated by an extensive 600 MHz NMR analysis including 1D and 2D NMR experiments as well as ESI-MS. Among the seven isolated saponins, two have never been reported before : 3…

Organic ChemistryPharmaceutical ScienceFabaceaeSweet taste receptorsWisteria sinensisTAS1R2/TAS1R3Analytical ChemistryChemistry (miscellaneous)Drug Discovery[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyMolecular Medicine<i>Wisteria sinensis</i>; Fabaceae; triterpene glycosides; sweet taste; TAS1R2/TAS1R3Physical and Theoretical Chemistry2D-NMRMolecules
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Oleanane-type saponins from the roots of Wisteria floribunda macrobotrys

2016

PharmacologybiologyTraditional medicineWisteriaOrganic ChemistryPharmaceutical ScienceFabaceaeWisteria floribundabiology.organism_classificationDiagnostic toolsAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicinechemistryDrug DiscoveryMolecular MedicineOleananePlanta Medica
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Hypoglycaemic effect of Spergularia purpurea in normal and streptozotocin-induced diabetic rats

2000

Single and repeated oral administration of the water extracts of Spergularia purpurea (SP) at a dose of 10 mg/kg were tested on hypoglycaemic activity in normal and streptozotocin-induced diabetic rats. In normal rats, the water extract of SP decreased significantly the plasma glucose levels 4 h after single oral administration (P0.01), and one week after repeated oral administration (P0.05). A significant decrease of plasma glucose levels was observed 6 h after a single oral administration of the water extract of S. purpurea in severe hyperglycaemic rats (n=6) from 22.78+/-0.60 to 11.21+/-0.49 mmol/l (P0.001). On other hand, water extract of S. purpurea normalised plasma glucose levels aft…

Blood GlucoseMalemedicine.medical_specialtyBlood sugarPharmacognosyDiabetes Mellitus Experimentallaw.inventionLethal Dose 50MicelawOral administrationInternal medicineDiabetes mellitusDrug DiscoverymedicineAnimalsHypoglycemic AgentsInsulinRats WistarPharmacologyPlants MedicinalBehavior AnimalPlant Extractsbusiness.industryBody Weightmedicine.diseaseStreptozotocinRatsMoroccoEndocrinologyPhytochemicalToxicityPhytotherapybusinessmedicine.drugJournal of Ethnopharmacology
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A review on the phytopharmacological studies of the genus Polygala

2020

Abstract Ethnopharmacological relevance The genus Polygala, the most representative genus of the Polygalaceae family, comprises more than 600 species from all over the world of which around 40 are distributed in China, some of them, being used in the Traditional Chinese Medicine system. Aim of the review We intend to discuss the current knowledge about the traditional uses, and the newest phytochemical and pharmacological achievements with tentative elucidation of the mechanism of action on the genus Polygala covering the period 2013–2019 to provide a scientific support to the traditional uses, and to critically analyze the reported studies to obtain new insights for further researches. Mat…

ChinaPolygala[SDV]Life Sciences [q-bio]Traditional Chinese medicine03 medical and health sciences0302 clinical medicineGenusDrug DiscoveryAnimalsHumansMedicine Chinese Traditional030304 developmental biologyPharmacology0303 health sciencesbiologyTraditional medicinebiology.organism_classificationPolygala3. Good healthDisease Models AnimalPhytochemical030220 oncology & carcinogenesisEthnopharmacologyElectronic dataPolygalaceaePlant PreparationsEnzyme inhibitoryPhytotherapyJournal of Ethnopharmacology
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Saponins as immunoadjuvants and immunostimulants

1999

Saponins are either triterpene or steroid glycosides widely distributed in the plant and animal kingdom and include a large number of biologically active compounds. Most of them have surface-active and cholesterol-binding properties.

chemistry.chemical_classificationbiologyTraditional medicineQuillaja saponariaChemistrymedicine.medical_treatmentGlycosideBiological activitySimian immunodeficiency virusmedicine.disease_causebiology.organism_classificationSteroidTriterpenemedicine
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Chemical constituents from Phlomis bovei Noë and their chemotaxonomic significance

2020

Abstract A phytochemical investigation of the leaves and roots of Phlomis bovei Noe (Lamiaceae) led to the isolation of sixteen compounds, including iridoids (1, 2, 3), megastigmanes (4, 5), phenylpropanoids (6, 7, 8, 9, 10), lignans (11, 12, 13, 14), a nortriterpene (15), and a phenyl glucoside (16). Compounds (1, 2, 4, 5, 6, 10) were obtained from the leaves and compounds (1, 2, 3, 7, 8, 9, 11, 12, 13, 14, 15, 16) were isolated from the roots. Compounds 1 and 2 were found both in the leaves and in roots. The compounds were identified by analysis of 1D- (1H, 13C), 2D-NMR (1H–1H COSY, TOCSY, ROESY, HSQC, HMBC) spectroscopic data, mass spectrometry (ESI- and HR-ESI-MS), and by comparison wit…

biology010405 organic chemistryStereochemistrybiology.organism_classification01 natural sciencesBiochemistry0104 chemical sciences010404 medicinal & biomolecular chemistryMegastigmaneschemistry.chemical_compoundPhlomisPhytochemicalGlucosidechemistryChemical constituentsLamiaceaeSpectral dataEcology Evolution Behavior and SystematicsPhlomis boveiBiochemical Systematics and Ecology
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A dammarane-type saponin from the roots of Ampelozizyphus amazonicus.

1993

A new C31 dammarane-type triterpenoid saponin has been isolated from the roots of Ampelozizyphus amazonicus. Its structure was elucidated to be ampelozigenin-15 alpha-O-acetyl- 3-O-alpha-L-rhamnopyranosyl-(1--2)-beta-D-glucopyranoside by 1D and 2D NMR spectroscopic methods, and by chemical transformations. Ampelozigenin is a novel triterpene, (20R,22R)-16 beta,22:16 alpha, 30-diepoxydammar-24(24')- methylene-3 beta, 15 alpha, 20-triol.

chemistry.chemical_classificationAmpelozizyphusMagnetic Resonance SpectroscopyPlants MedicinalbiologyStereochemistryDammaraneMolecular Sequence DataSaponinPlant ScienceGeneral MedicineHorticultureSaponinsbiology.organism_classificationBiochemistryTriterpeneschemistry.chemical_compoundTriterpenechemistryCarbohydrate SequenceRhamnaceaeMolecular BiologyTwo-dimensional nuclear magnetic resonance spectroscopyTriterpenoid saponinPhytochemistry
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Triterpenoid saponins from the cultivar “Green Elf” of Pittosporum tenuifolium

2021

Four oleanane-type glycosides were isolated from a horticultural cultivar “Green Elf” of the endemic Pittosporum tenuifolium (Pittosporaceae) from New Zealand: three acylated barringtogenol C glycosides from the leaves, with two previously undescribed 3-O-β-d-glucopyranosyl-(1→2)-[α-l-arabinopyranosyl-(1→3)]-β-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C, 3-O-β-d-galactopyranosyl-(1→2)-[α-l-arabinopyranosyl-(1→3)]-β-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C, and the known 3-O-β-d-glucopyranosyl-(1→2)-[α-l-arabinopyranosyl-(1→3)]-β-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C (Eryngioside L). From the roots, the known 3-O-β-d-glucopyra…

PittosporaceaeSaponinPittosporaceaePharmaceutical ScienceOrganic chemistry01 natural sciencesTAS1R2/TASR3Analytical ChemistryTriterpenoidTAS1R3QD241-441sweet tasteDrug Discovery[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyCultivarPhysical and Theoretical Chemistrytaste inhibitor2. Zero hungerchemistry.chemical_classificationbiologyTraditional medicine010405 organic chemistryPittosporum tenuifoliumbarringtogenol CGlycosideSweet tastebiology.organism_classification0104 chemical sciencesPittosporum tenuifolium010404 medicinal & biomolecular chemistry<i>Pittosporum tenuifolium</i>chemistryChemistry (miscellaneous)Molecular Medicine[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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Induction of Neuronal Differentiation in Neurosphere Stem Cells by Ellagic Acid Derivatives

2009

A bioassay-guided fractionation of methanol extracts of stem barks, combined with screening based on Epidermal Growth Factor (EGF)-responsive neural stem cells (erNSCs) differentiation assay, has been used. This study resulted in the isolation of 3,3′-di- O-methylellagic acid 1, 3,3′-di- O-methyl ellagic acid-4- O-β-D-xylopyranoside 2, ellagic acid 3, and arjunolic acid 4. Among them, compounds 1 and 2 exhibit potent induction of neuronal differentiation in neurosphere stem cells with no cytotoxic effect. These results indicate that compounds 1 and 2 may be useful as pharmacological agents for the treatment of neurodegenerative diseases. These compounds may account, for the use of T. super…

Nervous systemPlant ScienceChemical FractionationBiologyPharmacologyMicechemistry.chemical_compoundEllagic AcidEpidermal growth factorNeurosphereDrug DiscoveryBotanymedicineAnimalsCytotoxic T cellCells CulturedNeuronsPharmacologyStem CellsCell DifferentiationGeneral MedicineIn vitroNeural stem cellmedicine.anatomical_structureComplementary and alternative medicinechemistryTerminaliaStem cellEllagic acidNatural Product Communications
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Glycoside derivatives of scopoletin and β-sitosterol from Hymenodictyon floribundum

2003

chemistry.chemical_classificationchemistry.chemical_compoundRubiaceaeTraditional medicinechemistryScopoletinGlycosideHymenodictyon floribundumBiologybiology.organism_classificationBiochemistryEcology Evolution Behavior and SystematicsBiochemical Systematics and Ecology
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La génétique au service du goût : caractérisation de mutants pour l'accumulation de saponines et l'activité lipoxygènase dans la graines de pois (Pis…

2018

International audience

[SDV] Life Sciences [q-bio][SDE] Environmental Sciences[SDV]Life Sciences [q-bio][SDE]Environmental Sciences[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[SDV.BV] Life Sciences [q-bio]/Vegetal BiologyComputingMilieux_MISCELLANEOUS
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Secoiridoids and Xanthones fromGentianella nitida

1996

From Gentianella nitida twelve known metabolites were isolated and identified by HPLC-UV and/or by spectroscopic methods as secologanoside, amaroswerin, amarogentin (secoiridoids), isoorientin (C-glucosylflavone), mangiferin, demethylbellidifolin 8-O-glucoside, norswertianine 1-O-glucoside, swertianine 1-O-primeveroside, swertianine 8-O-glucoside, norswertianine, demethylbellidifolin, and swertianine (xanthone glycosides and aglycones). Secologanoside is reported here for the first time in Gentianaceae species ; the antioxidant mangiferin was obtained as the major compound in good yield.

Pharmacologychemistry.chemical_classificationGentianaceaeTraditional medicinebiologyIsoorientinOrganic ChemistryPharmaceutical ScienceGlycosidePharmacognosyAmarogentinbiology.organism_classificationAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicinechemistryGlucosideDrug DiscoveryBotanyXanthoneMolecular MedicineMangiferinPlanta Medica
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Natural Triterpene Glycosides for Antibody Recognition

2016

Multiple sclerosis is an autoimmune disease that affects the central nervous system. The key role of the glycosylation in disease pathogenesis has been previously studied and the synthetic N-glucosylated peptide CSF114(Glc) proved its efficiency in autoantibody recognition in the sera of multiple sclerosis patients. Herein, pure natural triterpene glycosides containing different glycosyl moieties were isolated and tested in multiple sclerosis patientsʼ sera to better understand the role of glycosylation. They were selected taking into account the nature and complexity of their osidic part. Five triterpene glycosides were isolated from several plants with more than 95 % purity. The interacti…

Autoimmune diseasechemistry.chemical_classificationGlycosylationMultiple sclerosisAutoantibodyGlycosidemacromolecular substancesBiologymedicine.diseasecarbohydrates (lipids)chemistry.chemical_compoundAntigenTriterpenechemistryBiochemistryImmunologymedicinebiology.proteinAntibodybiomarkers • autoantibody recognition autoimmune disease multiple sclerosis triterpene glycosidesPlanta Medica Letters
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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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