Search results for "LEAN"

showing 10 items of 3611 documents

Determination of soyasaponins I and βg in raw and cooked legumes by solid phase extraction (SPE) coupled to liquid chromatography (LC)-mass spectrome…

2013

Legumes contain a rich variety of phytochemicals as soyasaponins, triterpenoidal glycosides that possess multiple health-promoting properties, such as lowering of cholesterol. In this work, the quantification of soyasaponins I and βg in 60 raw and cooked legumes by using a solid phase extraction (SPE) coupled to a liquid chromatography (LC)-mass spectrometry (MS) method was carried out. Results showed that lentils are a good source of soyasaponins, with a content of soyasaponin I that ranged from 636 to 735 mg kg(-1) and of soyasaponin βg from 672 to 1807 mg kg(-1). The cooking process produced a small loss of soyasaponins in water, that is, 4.8-8.7%, and partially converted soyasaponin βg …

chemistry.chemical_classificationSoyasaponin IChromatographyCooking processSolid Phase ExtractionGlycosideBiological AvailabilityFabaceaeGeneral ChemistrySaponinsMass spectrometryIn vitro digestionMass SpectrometrychemistryLiquid chromatography–mass spectrometryHumansDigestionSolid phase extractionOleanolic AcidGeneral Agricultural and Biological SciencesDigestionChromatography High Pressure LiquidJournal of agricultural and food chemistry
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Polyacanthoside A, a new oleanane-type triterpenoid saponin with cytotoxic effects from the leaves of Acacia polyacantha (Fabaceae)

2018

The chemical investigation of the leaves and stem bark of Acacia polyacantha (Fabaceae) led to the isolation of a new oleanane-type triterpenoid saponin named polyacanthoside A 1 together with fifteen known compounds. Their structures were established from spectral , mainly HRESIMS, 1D NMR and 2D NMR and by comparison with literature data. The cytotoxicity of compound 1 and the analogues 8 as well as doxorubicin was determined in a panel of 9 cancer cell lines including sensitive and drug resistant phenotypes. Unlike the analogue 8, compound 1 as well as doxorubicin displayed cytotoxic effects in all the 9 tested cancer cell lines with IC50 values ranged from 8.90 μM (towards CCRF-CEM leuke…

chemistry.chemical_classificationStem barkbiologyTraditional medicine010405 organic chemistryChemistryOrganic ChemistryAcaciaPlant ScienceFabaceaebiology.organism_classification01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistry010404 medicinal & biomolecular chemistrychemistry.chemical_compoundCytotoxic T cell3-O-methyl-D-chiro-inositolOleananeTriterpenoid saponin
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Restricted rotation in unbridged sandwich complexes: rotational behavior of closo-[Co(eta 5-NC4H4)(C2B9H11)] derivatives.

2005

Rotation about the centroid/ metal/centroid axis in ferrocene is facile; the activation energy is 1-5 kcal mol - 1 . The structurally similar sandwich complexes derived from closo-[3-Co(η 5 -NC 4 H 4 )-1,2-C 2 B 9 H 1 1 ] (1) have a different rotational habit. In 1, the cis rotamer in which the pyrrolyl nitrogen atom bisects the carboranyl cluster atoms is 3.5 kcal mol - 1 more stable in energy than the rotamer that is second lowest in energy. This cis rotamer is wide, spanning 216°, and may be split into three rotamers of almost equal energy by substituting the N and the carboranyl carbon atoms adequately. To support this statement, closo-[3-Co(η 5 -NC 4 H 4 )-1,2-(CH 3 ) 2 -1,2-C 2 B 9 H …

chemistry.chemical_classificationSteric effects010405 organic chemistryStereochemistryOrganic ChemistryHeteroatomGeneral Chemistry010402 general chemistry7. Clean energy01 natural sciencesCatalysis0104 chemical sciencesRotational energyIonElectronegativitychemistry.chemical_compoundCrystallographychemistryFerroceneCounterionConformational isomerismChemistry (Weinheim an der Bergstrasse, Germany)
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Phytochemical analysis of two Weigela florida cultivars, “Pink Poppet” and “Jean’s Gold”

2020

Abstract Nine different oleanane-type glycosides were extracted and isolated by various chromatographic methods from two Weigela florida cultivars, “Pink Poppet” and “Jean’s Gold”. From the roots of W. florida “Pink Poppet”, three monodesmosidic oleanolic acid saponins 1, 4, 5 were obtained, together with one hederagenin ester 6 from the leaves, and six bidesmosidic saponins 2, 3, 6-9 were isolated from the leaves of W. florida “Jean’s Gold”. Among compounds 1-9, three were previously undescribed (1-3) and six (4-9) were already published in the literature. Their structures were assigned by spectroscopic analysis mainly 2D NMR and mass spectrometry (ESI-MS). The cytotoxicity of the isolated…

chemistry.chemical_classificationTraditional medicine010405 organic chemistryChemistryGlycosidePlant Science01 natural sciencesBiochemistry0104 chemical sciences010404 medicinal & biomolecular chemistrychemistry.chemical_compoundHederageninMouse ColonPhytochemicalWeigela floridaCultivarCytotoxicityAgronomy and Crop ScienceOleanolic acidBiotechnologyPhytochemistry Letters
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Triterpenoid saponins from Piptadeniastrum africanum (Hook. f.) Brenan

2013

One new triterpenoid saponin, named piptadeniaoside (1), along with two known saponins (2–3) have been isolated from the stem bark of Piptadeniastrum africanum. After previous isolation of flavone derivatives from this plant, new phytochemical investigations were performed for its saponin content. Their structures were established by direct interpretation of their spectral data, mainly HRESIMS, 1D NMR (1H, 13C NMR, DEPT) and 2D NMR (COSY, NOESY, HSQC and HMBC), and by comparison with the literature data.

chemistry.chemical_classificationTraditional medicineChemistryStereochemistrySaponinPlant ScienceDEPTCarbon-13 NMRBiochemistrychemistry.chemical_compoundPhytochemicalAgronomy and Crop ScienceTwo-dimensional nuclear magnetic resonance spectroscopyOleanolic acidHeteronuclear single quantum coherence spectroscopyBiotechnologyTriterpenoid saponinPhytochemistry Letters
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Triterpene saponins from Schefflera abyssinica

2006

chemistry.chemical_classificationchemistry.chemical_compoundHederageninbiologyTriterpenechemistryTraditional medicineAraliaceaebiology.organism_classificationBiochemistryOleanolic acidEcology Evolution Behavior and SystematicsScheffleraBiochemical Systematics and Ecology
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Biologically and Pharmacologically Active Saponins from Plants: Recent Advances

2000

Saponins as triterpene or steroid glycosides were well known in ancient times for their detergent, haemolytic and fish toxic activities, properties which are correlated with the amphiphilic character of the molecules and their ability to complex cholesterol.

chemistry.chemical_classificationchemistry.chemical_compoundchemistryBiochemistryTriterpeneCholesterolmedicine.medical_treatmentAmphiphilemedicineGlycosideFish <Actinopterygii>Oleanolic acidSteroid
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Structure elucidation of new oleanane-type glycosides from three species of Acanthophyllum

2010

From the roots of three species of Acanthophyllum (Caryophyllaceae), two new gypsogenic acid glycosides, 1 and 2, were isolated, 1 from A. sordidum and A. lilacinum, 2 from A. elatius and A. lilacinum, together with three known saponins, glandulosides B and C, and SAPO50. The structures of 1 and 2 were established mainly by 2D NMR techniques as 23-O-β-D-galactopyranosylgypsogenic acid-28-O-β-D-glucopyranosyl-(13)-[β-D-glucopyranosyl-(16)]-β-D-galactopyranoside (1) and gypsogenic acid-28-O-β-D-glucopyranosyl-(13)-[β-D-glucopyranosyl-(16)]-β-D-galactopyranoside (2). The cytotoxicity of several of these saponins was evaluated against two human colon cancer cell lines (HT-29 and HCT 116). Copyr…

chemistry.chemical_classificationfood.ingredientbiologyStereochemistryGlycosideCaryophyllaceaeGeneral Chemistrybiology.organism_classificationAcanthophyllumHuman colon cancerchemistry.chemical_compoundfoodchemistryGeneral Materials ScienceCytotoxicityTwo-dimensional nuclear magnetic resonance spectroscopyOleananeMagnetic Resonance in Chemistry
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Photovoltaic effect in bulk heterojunction system with glass forming indandione derivative DMABI-6Ph

2018

The aim of the work is to evaluate possible use of 2-[[4-(bis(2-trityloxyethyl)amino)phenyl]methylene]indane-1,3-dione (DMABI-6Ph) as light absorbing material for solar cells. DMABI-6Ph is a perspective material due to its good photoelectrical, thermal and chemical properties. The main advantage of DMABI-6Ph is its ability to form amorphous films by wet-casting methods thus allowing using the compound in organic solar cells made from solution. For now most popular materials for solution processable solar cells are polymer P3HT and fullerene derivative PCBM, but lot of investigations are in the field of new low molecular weight materials to replace the polymer. Photoelectrical measurements w…

chemistry.chemical_classificationglass forming structureFullereneMaterials scienceOrganic solar cellOpen-circuit voltage020209 energybulk heterojunction02 engineering and technologyPolymerPhotovoltaic effect021001 nanoscience & nanotechnology7. Clean energyPolymer solar cellpower conversion efficiencyAmorphous solidchemistryChemical engineeringElectron affinity:NATURAL SCIENCES:Physics [Research Subject Categories]0202 electrical engineering electronic engineering information engineeringenergy levels0210 nano-technologyindandione groupEnergy Procedia
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The role of paraoxonase 1 (PON1) as an oxidation marker, in muscle improvement after increased beta-hydroxybutyrate (BHB) in blood, in patients with …

2020

Various studies have concluded that in multiple sclerosis (MS) metabolic changes related to energy alterations are generated at the mitochondrial level. These changes produce loss of muscle mass and lead to high levels of oxidative stress related to low levels of the enzyme Paraoxonase 1 (PON1). The ketone bodies, mainly beta-hydroxybutyrate (BHB), restore this energetic alteration by improving muscular activity. This pilot study was conducted over 4 months with 51 patients diagnosed with MS, randomly divided into: an intervention group that received an isocaloric diet of a Mediterranean origin supplemented with 60 ml of coconut oil; and a control group that received the same base diet but …

chemistry.chemical_classificationmedicine.medical_specialtyfood.ingredientbiologybusiness.industryMultiple sclerosisCoconut oilParaoxonasemedicine.diseasemedicine.disease_causePON1EndocrinologyfoodEnzymechemistryInternal medicineKetone bodiesmedicineLean body massbiology.proteinbusinessOxidative stressProceedings of 1st International Electronic Conference on Brain Sciences
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