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showing 10 items of 1466 documents

Chemical Composition and Antibacterial Activity of Extracts of Helleborus bocconei Ten. subsp. intermedius

2007

Helleborus bocconei Ten. subsp. intermedius (Ranunculaceae) is a Sicilian medicinal plant used for the treatment of pneumonia affecting cows and horses and for the removal of human decayed molars. The goal of our study was to assess the biological activity of Helleborus bocconei subsp. intermedius by testing its extracts for their activity against bacteria known to cause respiratory diseases. The two more active extracts (light petroleum from roots and aerial parts), as well as the dichloromethane extracts, were analyzed by GC/MS and their composition is reported.

PharmacologyTraditional medicine010405 organic chemistryHelleborusRanunculaceaePlant ScienceGeneral MedicineBiologymedicine.diseasebiology.organism_classification01 natural sciences0104 chemical sciences010404 medicinal & biomolecular chemistryComplementary and alternative medicineDrug DiscoverymedicineAntibacterial activityChemical compositionPneumonia (non-human)Natural Product Communications
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Essential Oil from Sideritis funkiana

1986

PharmacologyTraditional medicineOrganic ChemistryPharmaceutical ScienceBiologybiology.organism_classificationAnalytical Chemistrylaw.inventionComplementary and alternative medicinelawDrug DiscoverySideritisMolecular MedicineEssential oilPlanta Medica
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Spirostane-Type Saponins from Dracaena fragrans Yellow Coast

2015

Three steroidal glycosides were isolated from the bark of Dracaena fragrans (L.) Ker Gawl. « Yellow Coast », and a fourth from the roots and the leaves. Their structures were characterized on the basis of extensive 1D and 2D NMR experiments and mass spectrometry, and by comparison with NMR data of the literature. These saponins have the spirostane-type skeleton and are reported in this species for the first time.

PharmacologyTraditional medicineSteroidal glycosidesDracaena fragransPhytosterolsPlant ScienceGeneral MedicineSaponinsBiologybiology.organism_classificationComplementary and alternative medicinevisual_artDrug Discoveryvisual_art.visual_art_mediumBarkDracaena
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GC and GC/MS analysis of the essential oil of Salvia hierosolymitana boiss. Growing wild in Lebanon

2007

The essential oil of the aerial parts of Salvia hierosolymitana Boiss. (Lamiaceae), growing wild in Lebanon, was obtained by hydrodistillation and analysed by GC and GC-MS. Ninety-two compounds, representing 92.7% of the oil, were identified. The major components were hexadecanoic acid (15.5%), phytol (5.4%), hexahydrofarnesyl acetone (4.6%), (Z,Z)-9,12-octadecadienoic acid (4.5%) and 4-vinylguaiacol (4.4%).

PharmacologyTraditional medicinebiology010405 organic chemistryPlant ScienceGeneral Medicinebiology.organism_classification01 natural sciencesSalvia hierosolymitana0104 chemical scienceslaw.invention010404 medicinal & biomolecular chemistryComplementary and alternative medicinelawDrug DiscoveryGas chromatography–mass spectrometryEssential oil
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Effect of Marrubium globosum ssp libanoticum on intestinal motility

2007

PharmacologyTraditional medicinebiologybusiness.industryOrganic ChemistryPharmaceutical Sciencebiology.organism_classificationAnalytical ChemistryIntestinal motilityComplementary and alternative medicineDrug DiscoveryMolecular MedicineMedicinebusinessMarrubium
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Anti-Inflammatory Activity of a Flavone from Sideritis leucantha.

1986

PharmacologyTraditional medicinemedicine.drug_classOrganic ChemistryPharmaceutical ScienceBiologybiology.organism_classificationAnti-inflammatoryAnalytical ChemistryComplementary and alternative medicineDrug DiscoverymedicineMolecular MedicineSideritis leucanthaPlanta medica
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Cytotoxic Bufadienolides from the Leaves of Melianthus major

2020

Melianthus major is a medicinal plant endemic to South Africa. Its leaf extract led to the isolation of five new bufadienolides, 2β-acetoxy-3,5-di-O-acetylhellebrigenin (1), 2β-acetoxy-3-O-acetylhellebrigenin (2), 2β-acetoxy-14-deoxy-15β,16β-epoxymelianthugenin (4), 2β-acetoxy-14-deoxy-15β,16β-epoxymelianthusigenin (5), and 2β-hydroxymelianthusigenin (6), and four known analogues. The structures of the compounds were elucidated using NMR and HRESIMS data analyses. The relative configurations were defined by single-crystal X-ray crystallography and NOESY correlations. The isolated compounds exhibited strong cytotoxicity against MCF-7 breast cancer cells and sensitive CCRF-CEM and multidrug-r…

Pharmacologybiology010405 organic chemistryChemistryCcrf cemOrganic ChemistryPharmaceutical Sciencemedicine.diseasebiology.organism_classification01 natural sciencesMolecular biologyMelianthus major0104 chemical sciencesAnalytical Chemistry010404 medicinal & biomolecular chemistryLeukemiaComplementary and alternative medicineDrug DiscoverymedicineIc50 valuesMolecular MedicineCytotoxic T cellBreast cancer cellsCytotoxicityTwo-dimensional nuclear magnetic resonance spectroscopyJournal of Natural Products
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The Diterpenoids of the Genus Marrubium (Lamiaceae)

2006

The occurrence and chemical structures of labdane diterpenoids from the genus Marrubium are reviewed and the published 13C NMR spectroscopic data for these compounds is presented. The pharmacological activities and biogenesis of these diterpenoids are also reported.

Pharmacologybiology010405 organic chemistryPlant ScienceGeneral Medicinebiology.organism_classification01 natural sciences0104 chemical sciencesLabdane010404 medicinal & biomolecular chemistrychemistry.chemical_compoundComplementary and alternative medicinechemistryGenusDrug DiscoveryBotanyLamiaceaeMarrubiumNatural Product Communications
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Dioncophyllines C2, D2, and F and related naphthylisoquinoline alkaloids from the Congolese liana Ancistrocladus ileboensis with potent activities ag…

2017

Dioncophylline F (1), the first 5,8'-coupled dioncophyllaceous alkaloid (i.e., lacking an oxygen function at C-6 and possessing an R-configuration at C-3), was isolated from the recently described Congolese liana Ancistrocladus ileboensis. Two further, likewise Dioncophyllaceae-type, alkaloids, the dioncophyllines C2 (2) and D2 (3), were identified, along with the Ancistrocladaceae-type compound ancistrocladisine B (4), which is oxygenated at C-6 and S-configured at C-3. The structures of the new compounds were determined by spectroscopic, chemical, and chiroptical methods. The stereostructure of 1 was further confirmed by total synthesis. As a consequence of the lack of a methyl group orth…

Pharmacologybiology010405 organic chemistryStereochemistryAlkaloidOrganic ChemistryPharmaceutical ScienceTotal synthesisPlasmodium falciparum010402 general chemistrybiology.organism_classification01 natural sciencesLeukemia cell line0104 chemical sciencesAnalytical ChemistryAncistrocladus ileboensischemistry.chemical_compoundComplementary and alternative medicineLianachemistryDrug DiscoveryMolecular MedicineAncistrocladaceaeMethyl group
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New Eudesmanolides Related to Torrentin from Artemisia herba-alba subsp. valentina.

1991

The reinvestigation of aerial parts of A. herba- alba subsp. valentina afforded four new eudesmanolides, all of them closely related to torrentin. Their structures were deduced by spectroscopic and chemical methods

PharmacologybiologyArtemisia herba-albaChemistryOrganic ChemistryPharmaceutical SciencePharmacognosybiology.organism_classificationAnalytical ChemistryComplementary and alternative medicineDrug DiscoveryBotanyMolecular MedicineArtemisiaPlanta medica
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