Search results for "Complement"

showing 10 items of 2113 documents

Chemical Composition of the Essential Oil of Zingiber Zerumbet Var. Darcyi

2012

The chemical composition of essential oil obtained by hydrodistillation method from the rhizomes of Z. zerumbet var. darcyi was determined by GC and GC-MS. Thirty-three compounds, accounting for 93.6% of the oil were identified including twenty compounds in minor (0.1-0.6%) and eight in trace (<0.05%) amounts. The main compounds were zerumbone (69.9%) α-humulene (12.9%), humulene epoxide II (2.5%), caryophyllene oxide (1.1%) and camphene (1.9%). In this analysis, it has been found that the variety could be used as an additional new source of natural zerumbone besides Zingiber zerumbet. This is a first report on the analysis of Z. zerumbet var. darcyi oil.

PharmacologybiologyHumuleneTraditional medicinePlant ScienceGeneral Medicinebiology.organism_classificationlaw.inventionRhizomechemistry.chemical_compoundComplementary and alternative medicinechemistryZingiber zerumbetlawDrug DiscoveryBotanyCampheneZingiberaceaeGas chromatography–mass spectrometryChemical compositionEssential oilNatural Product Communications
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Expression of the human complement C8 subunits is independently regulated by interleukin 1β, interleukin 6, and interferon γ

1998

The eighth component of human complement (C8) is composed of two subunits which are products from three separate genes. The alpha-gamma- and the beta-subunit of C8 are expressed independently, and are part of the membrane attack complex. C8 is primarily synthesized in the liver. It has been shown in previous studies that the human hepatoma cell line HepG2 constitutively expresses C8, and thus is a suitable model system for studying C8 biosynthesis in vitro. Expression is modulated by the cytokines IL-1 beta, IL-6 and IFN-gamma. The effect of the different cytokines on the expression of these subunits was examined using biosynthetical labelling and immunoprecipitation methods. C8 alpha-gamma…

PharmacologybiologyInterleukin-6ImmunoprecipitationAntineoplastic AgentsSulfur RadioisotopesComplement C8Precipitin TestsMolecular biologyIn vitroComplement systemInterferon-gammaGene expressionTumor Cells Culturedbiology.proteinHumansSecretionInterleukin 6Beta (finance)Complement membrane attack complexInterleukin-1Immunopharmacology
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Minor diterpenoids from Scutellaria polyodon.

2000

Four minor neoclerodane diterpene constituents were isolated from the aerial parts of Scutellaria polyodon. These compounds were characterized as the new scupolins J (1) and K (2) and the previously known scutalpin O (3) and scutalsin.

PharmacologybiologyMolecular StructureChemistryStereochemistrySpectrum AnalysisOrganic ChemistryPharmaceutical SciencePlantsbiology.organism_classificationTerpenoidAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicineDrug DiscoveryScutellariaMolecular MedicineHemiacetalDiterpeneDiterpenesJournal of natural products
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Volatile Components from Aerial parts of Centaurea gracilenta and C. ovina ssp. besserana Growing Wild in Bulgaria

2011

The essential oils of Centaurea gracilenta Velen. (CG) and C. ovina Pall. ex Willd. ssp. besserana (DC.) Dostál (COB) growing wild in Bulgaria, were studied by GC and GC-MS. Forty-five compounds for CG, representing the 90.1% of the oil, and 68 compounds for COB, representing the 91.9% of the oil, were identified. The oils were rich in sesquiterpenoids (33.4% for CG and 27.3% for COB), hydrocarbons (28.3% for CG and 10.7% for COB) and carbonylic compounds (12.7% for CG and 13.1% for COB). Fatty acids were abundant only for COB (31.3%). β-Eudesmol (12.8%), nonacosane (11.8%) and p-vinyl guiacol (7.5%) were recognized as the main constituents for CG, while hexadecanoic acid (21.4%), spathule…

PharmacologybiologyNonacosanePlant ScienceGeneral Medicinebiology.organism_classificationSpathulenolchemistry.chemical_compoundComplementary and alternative medicineCaryophyllene oxidechemistryCentaureaDrug DiscoveryBotanyNatural Product Communications
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Volatile components and antifeedant activity of the essential oil from Scutellaria hastifolia L.

2009

PharmacologybiologyOrganic ChemistryPharmaceutical ScienceSettore CHIM/06 - Chimica Organicabiology.organism_classificationAnalytical Chemistrylaw.inventionComplementary and alternative medicineScutellaria hastifolia L.essential oil antifeedant activitylawDrug DiscoveryBotanyScutellariaMolecular MedicineEssential oil
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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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Triterpenoid Saponins From the Root Bark of Haplocoelum congolanum

2019

Two undescribed triterpenoid saponins together with 5 known ones were isolated from the root bark of Haplocoelum congolanum Hauman. Their structures were elucidated by spectroscopic methods including one-dimensional and two-dimensional nuclear magnetic resonance experiments in combination with mass spectrometry as 3- O-(4- O-[3-hydroxy-3-methylglutaryl])-α-l-arabinopyranosyl-(1→3)-α-l-rhamnopyranosyl-(1→2)-[β-d-glucopyranosyl-(1→4)]-α-l-arabinopyranosyloleanolic acid and 3- O-α-l-arabinofuranosyl-(1→3)-α-l-rhamnopyranosyl-(1→2)-[β-d-glucopyranosyl-(1→4)]-α-l-arabinopyranosyloleanolic acid.

PharmacologybiologyTraditional medicine010405 organic chemistryChemistryPlant ScienceGeneral MedicineSapindaceaebiology.organism_classification01 natural sciences0104 chemical sciences010404 medicinal & biomolecular chemistryHaplocoelumTriterpenoidComplementary and alternative medicinevisual_artDrug Discoveryvisual_art.visual_art_mediumBarkNatural Product Communications
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Volatile constituents of Scutellaria rubicunda Hornem subsp. linnaeana (Caruel) Rech. (Lamiaceae) endemic in Sicily

2006

PharmacologybiologyTraditional medicineCaryophylleneOrganic ChemistryVolatileScutellaria rubicunda HornemPharmaceutical Sciencebiology.organism_classificationBiochemistrylaw.inventionAnalytical Chemistrychemistry.chemical_compoundLinaloolchemistryComplementary and alternative medicinelawDrug DiscoveryBotanyScutellariaMolecular MedicineLamiaceaeSpodoptera littoralisEcology Evolution Behavior and SystematicsEssential oilPlanta Medica
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Cytotoxic properties of Marrubium globosum ssp. libanoticum and its bioactive components

2013

Marrubium globosum Montbr. et Auch. ex Benth. ssp. libanoticum Boiss. (Lamiaceae) is a medicinal plant used in Lebanon for the treatment of inflammatory diseases, asthma, coughs and other pulmonary and urinary problems. The goal of our study was to assess the biological activity of M. globosum by testing different extracts of the aerial parts for their antiproliferative activity against human melanoma cells using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The chloroform fraction showed the greatest activity. The compounds isolated from the extracts were also tested: the mixture of (13 S)-9α,13α-epoxylabda-6β(19),16(15)-diol dilactone and (13 R)-9α,13α-epo…

PharmacologybiologyTraditional medicineChemistryCytotoxicityPlant ScienceGeneral MedicineSettore CHIM/06 - Chimica OrganicaMarrubium globosum Lebanon antiproliferative activitybiology.organism_classificationLabdane diterpenoidPhenolic compoundsComplementary and alternative medicineDrug DiscoveryMarrubium globosum libanoticumCytotoxic T cellSettore BIO/15 - Biologia FarmaceuticaMelanomaMarrubium
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Two New Eudesmanolides from Artemisia caerulescens subsp. gargantae.

1990

PharmacologybiologyTraditional medicineOrganic ChemistryArtemisia caerulescensPharmaceutical SciencePharmacognosybiology.organism_classificationIsolation (microbiology)Analytical ChemistryComplementary and alternative medicineDrug DiscoveryBotanyMolecular MedicineArtemisiaPlanta medica
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