Search results for "diterpene"

showing 10 items of 139 documents

Arthrinins A–D: Novel diterpenoids and further constituents from the sponge derived fungus Arthrinium sp.

2011

Bioassay-guided fractionation of a methanolic extract of the fungus Arthrinium sp., isolated from the Mediterranean sponge Geodia cydonium, afforded 10 natural products including five new diterpenoids, arthrinins A-D (1-4) and myrocin D (5). In addition, five known compounds were obtained, which included myrocin A (6), norlichexanthone (7), anomalin A (8), decarboxycitrinone (9) and 2,5-dimethyl-7-hydroxychromone (10). The structures of all isolated compounds were unambiguously elucidated based on extensive 1D and 2D NMR and HR-MS analyzes. The absolute configuration of arthrinins A-D (1-4) was established by the convenient Mosher method performed in NMR tubes and by interpretation of the R…

Vascular Endothelial Growth Factor AClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsBiochemistryMiceAscomycotaCell Line TumorNeoplasmsDrug DiscoveryAnimalsHumansMTT assayCytotoxicityProtein Kinase InhibitorsMolecular BiologyNeovascularization PathologicKinaseChemistryOrganic ChemistryTerpenoidIn vitroPoriferaEndothelial stem cellVascular endothelial growth factor ABiochemistryCell cultureMolecular MedicineDiterpenesProtein KinasesBioorganic & Medicinal Chemistry
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Contribution of vitamin A to the oxidation resistance of human low density lipoproteins.

1995

This study investigated the antioxidant contribution of vitamin A in protecting human low density lipoprotein (LDL) against copper-stimulated oxidation. The presence of small amounts of retinol (0.033 ± 0.012 nmol/mol LDL) and retinyl palmitate (0.036 ± 0.021 nmol/mol LDL) was routinely ascertained in the LDL. A single oral supplementation with 20,000 IU vitamin A caused a two- to three-fold increase of retinol and retinyl palmitate in the LDL isolated 8 h after the supplementation. In comparison to autologous-control LDL, vitamin A-enriched LDL were more resistant to oxidation, as expressed both by a clear delay in the onset of lipid peroxidation and by a reduction of the rate of conjugate…

VitaminAdultMaleRetinyl EstersAntioxidantFree RadicalsArteriosclerosismedicine.medical_treatmentRetinyl esterIn Vitro Techniquesmedicine.disease_causeBiochemistryAntioxidantsLDLLipid peroxidationchemistry.chemical_compoundFree radicalIn vivoPhysiology (medical)Retinyl palmitatemedicineHumansVitamin ARetinolRetinolMiddle AgedLipoproteins LDLKineticsOxidative StresschemistryBiochemistryAtherosclerosiLow-density lipoproteinlipids (amino acids peptides and proteins)FemaleLipid PeroxidationAntioxidantDiterpenesOxidation-ReductionOxidative stressCopperFree radical biologymedicine
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Vitamin A in parenteral nutrition: uptake and distribution of retinyl esters after intravenous application.

1989

Short-term parenteral application of vitamin A was examined in rats. Retinyl margarinate, which is chemically similar to physiological retinyl esters, was used in vitamin A-depleted rats to study uptake, distribution, and storage of retinyl esters in tissues. Vitamin A-depleted and Vitamin A-sufficient rats were infused with a micellar suspension of retinyl margarinate for 7 h and then killed at different times. Retinyl margarinate was directly taken up by all tissues examined. It appears that infusion of retinyl esters in micellar form provides a direct way to supply vitamin A to peripheral, vitamin A-dependent tissues. Therefore, a short-term infusion of retinyl esters with an emulsifier …

VitaminMalemedicine.medical_specialtyRetinyl EstersMedicine (miscellaneous)Retinyl esterschemistry.chemical_compoundPharmacokineticsInfusion ProcedureInternal medicineTestismedicineDistribution (pharmacology)AnimalsTissue DistributionIntestinal MucosaVitamin ALungChromatography High Pressure LiquidChromatographyNutrition and Dieteticsbusiness.industryVitamin A DeficiencyRetinolMetabolismRatsTracheaEndocrinologyParenteral nutritionchemistryLiverParenteral Nutrition TotalDiterpenesbusinessSpleenThe American journal of clinical nutrition
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Long-Term Administration of High Dose Vitamin A to Rats Does Not Cause Fetal Malformations: Macroscopic, Skeletal and Physicochemical Finds

1996

A rat model was used to investigate whether high oral doses of vitamin A lead to fetal malformations and to what extent retinyl esters (RES) are transferred from the mother to the fetuses. Retinol and RES concentrations in plasma behave similarly in rats and humans. When high concentrations of vitamin A are administered, plasma retinol concentrations remain relatively constant, whereas plasma RES increased in parallel with the dose. To achieve an elevation from approximately 150 to > 1525 nmol x L(-1) in the experimental group before mating, female Ibm: RORO (spf) rats were fed a maintenance diet enriched with 15.2 x 10(3) retinol equivalents (RE) x kg(-1) at the start and increased stepwis…

VitaminRetinyl Estersmedicine.medical_specialtyChemical PhenomenaRetinoic acidMedicine (miscellaneous)Biologychemistry.chemical_compoundPregnancyOral administrationInternal medicinemedicineAnimalsVitamin AMaternal-Fetal ExchangeChromatography High Pressure LiquidFetusNutrition and DieteticsChemistry PhysicalRetinolAbnormalities Drug-InducedRetinol EquivalentEstersTeratologyRatsEndocrinologychemistryToxicityFemaleDiterpenesThe Journal of Nutrition
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Diterpenes from Euphorbia segetalis

1998

Numerous new diterpenes including several with new skeletons have been obtained from Euphorbia segetalis.

biologyEuphorbiaceaePlant ScienceGeneral MedicineHorticulturebiology.organism_classificationBiochemistryLabdanechemistry.chemical_compoundchemistryEuphorbia segetalisBotanyDiterpeneMolecular BiologyPhytochemistry
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Ucriol, an epoxy-diterpene from Sideritis syriaca

1983

Abstract The isolation of a new epoxy-diterpene from the inflorescence of Sideritis syriaca (S. sicula Ucria) is described. Its structure and stereochemistry were established by spectroscopy and partial synthesis.

biologyPlant ScienceGeneral MedicineEpoxyHorticulturebiology.organism_classificationBiochemistrychemistry.chemical_compoundInflorescencechemistryvisual_artBotanyvisual_art.visual_art_mediumSideritisDiterpeneMolecular BiologyPhytochemistry
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Spirocurcasone, a diterpenoid with a novel carbon skeleton from Jatropha curcas.

2010

Spirocurcasone (14), a diterpenoid possessing the unprecedented "spirorhamnofolane" skeleton, was isolated from the root barks of Jatropha curcas, a plant extensively cultivated throughout the world, along with 11 known and two other new diterpenoids. The stereostructure of spirocurcasone was established using HRESIMS, NMR, and quantum mechanical calculation of the electronic circular dichroic (ECD) spectrum. Some of the isolated diterpenoids showed a potent activity against L5178Y, a mouse lymphoma cell line.

biologyPlant rootsMolecular StructureChemistryMouse LymphomaOrganic ChemistryCarbon skeletonJatrophaJatrophabiology.organism_classificationBiochemistryAntineoplastic Agents PhytogenicPlant RootsTerpenoidMicePlant BarkOrganic chemistryAnimalsPhysical and Theoretical ChemistryDiterpenesDrug Screening Assays AntitumorJatropha curcasSpirocurcasoneOrganic letters
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Antifeedant activity of neo-clerodane diterpenoids from Teucrium fruticans and derivatives of fruticolone

1999

The antifeedant activity of three neo-clerodane diterpenoids, fruticolone, isofruticolone and fruticolide from Teucrium fruticans was assessed using larvae of Spodoptera littoralis. Isofruticolone was one of the most potent of the Teucrium derived neo-clerodanes. Chemical modification of functional groups on fruticolone showed that its activity could be enhanced.

biologyStereochemistryBiological activityPlant ScienceGeneral MedicineHorticulturebiology.organism_classificationBiochemistryTerpenoidTeucriumchemistry.chemical_compoundchemistryNoctuidaeDiterpeneSpodoptera littoralisMolecular BiologyPhytochemistry
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The C-12 and C-20 configurations of some neo-clerodane diterpenoids isolated from Teucrium species

1986

Abstract A convenient and conclusive method for determining the C-12 stereochemistry of neo-clerodan-20,12-olide derivatives, even when only one epimer is available, is by 1H NMR NOE measurements. The C-12 configuration of 26 neo-clerodane diterpenoids isolated from Teucrium species has been re-examined by using this type of experiment. The results indicated that all the previous assignments were correct, except for teupyreinin, where the previously assigned C-12(S) configuration must be amended to C-12(R). This was confirmed by chemical transformations and additional 1H and 13C NMR studies. Furthermore, the NOE experiments allowed the assignment of a C-20(S) configuration for teuflavin, th…

biologyStereochemistryPlant ScienceGeneral MedicineHorticultureCarbon-13 NMRbiology.organism_classificationBiochemistryTeucriumchemistry.chemical_compoundchemistryProton NMRMoleculeEpimerDiterpeneMolecular BiologyPhytochemistry
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Rearranged abietane diterpenoids from the root of two Teucrium species

1992

Abstract From the root of Teucrium fruticans , two new rearranged abietane diterpenoids, teuvincenones F and G, have been isolated together with the known diterpene teuvincenone E. The acetone extract of the root of T. polium subsp. expansum yielded three previously known compounds (ferruginol and teuvincenones A and B) and two new 17(15 → 16)- abeo -abietane derivatives (teuvincenones H and I). The structures of the new diterpenoids [12,16-epoxy-11,14-dihydroxy-17(15 → 16), 18(4 → 3)- diabeo -abieta-3,5,8,11,13,15-hexaene-2,7-dione (teuvincenone F), (16 S )-12,16-epoxy-11,14-dihydroxy-17(15 → 16)- abeo -abieta-8,11,13-triene-3,7-dione (teuvincenone G), 12,16-epoxy-6,11,14-trihydroxy-17(15 …

biologyStereochemistryPlant ScienceGeneral MedicineHorticulturebiology.organism_classificationBiochemistryTeucrium poliumfood.foodTeucriumFerruginolchemistry.chemical_compoundfoodchemistryDiterpeneMolecular BiologyAbietanePhytochemistry
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