Search results for "medicinal"

showing 10 items of 2966 documents

Aqua complex of iron(III) and 5-chloro-3-(2-(4,4-dimethyl-2,6- dioxocyclohexylidene) hydrazinyl)-2-hydroxybenzenesulfonate: Structure and catalytic a…

2013

Abstract A water-soluble iron(III) complex [Fe(H2O)3(L)]·5H2O (1) was prepared by reaction of iron(III) chloride with 5-chloro-3-(2-(4,4-dimethyl-2,6-dioxocyclohexylidene)hydrazinyl)-2-hydroxy-benzenesulfonic acid (H3L). The complex was characterized by IR, 1H NMR and ESI-MS spectroscopies, elemental and X-ray crystal structural analyses. The coordination environment of the central iron(III) is a distorted octahedron, three sites being occupied by L3− ligand, which chelates in O,N,O fashion, while three other sites are filled with the water molecules. The uncoordinated water molecules are held in the channels of the overall 3D supramolecular structure by the carbonyl and sulfonyl groups of …

Sulfonylchemistry.chemical_classificationNitroaldol reactionHalogen bondStereochemistryLigandHydrogen bondOrganic ChemistrySupramolecular chemistryMedicinal chemistryAnalytical ChemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryNitroethaneta116SpectroscopyJournal of molecular structure
researchProduct

ChemInform Abstract: Asymmetric Conjugate Addition of Malonate Esters to α,β-Unsaturated N-Sulfonyl Imines: An Expeditious Route to Chiral δ-Aminoest…

2014

The asymmetric conjugate addition of malonate esters to α,β-unsaturated N-sulfonyl imines is catalyzed by PyBOX/La(OTf)3 complexes in the presence of 4 A MS. The reaction gives the corresponding E enamines bearing a stereogenic center at the allylic position with good yields and enantiomeric ratios up to 97:3. This reaction provides a synthetic entry to chiral δ-aminoesters and piperidones.

Sulfonylchemistry.chemical_classificationchemistry.chemical_compoundAllylic rearrangementAddition reactionMalonatechemistryGeneral MedicineEnantiomerMedicinal chemistryStereocenterConjugateCatalysisChemInform
researchProduct

Methyl [4-methoxy-3-(methylsulfonyloxy)benzoyl]formate

2005

The crystal structure of the title compound, C11H12O7S, confirms an earlier proposal concerning the regioselectivity of electrophilic substitution reactions of mesyl guaiacol.

Sulfonylchemistry.chemical_classificationchemistry.chemical_compoundElectrophilic substitutionChemistryRegioselectivityGeneral Materials ScienceFormateGeneral ChemistryCrystal structureGuaiacolCondensed Matter PhysicsMedicinal chemistryActa Crystallographica Section E Structure Reports Online
researchProduct

Polyaza[n](1,4)naphthalenophanes and polyaza[n](9,10)anthracenophanes

2002

Abstract A series of polyaza[n](1,4)naphthalenophanes and polyaza[n](9,10)anthracenophanes have been prepared by using the Fukuyama's protecting group (2- or 4-nitrophenyl sulfonyl) in a one-pot cyclization–deprotection reaction. Global yields for the purified products are comparable with those obtained for other polyazacyclophanes using the tosyl group as the amine protecting group. Their structural study has been carried-out by NMR showing a high rigidity for the smaller cycles and a more dynamic behaviour for the largest member of the series. The free energy barrier for the rotational equilibrium for compound 25 is about 3 kcal/mol lower than that calculated for analogous N-tosylated mac…

Sulfonylchemistry.chemical_classificationchemistry.chemical_compoundTosylchemistryStereochemistryOrganic ChemistryDrug DiscoveryAmine gas treatingProtecting groupBiochemistryMedicinal chemistryTetrahedron
researchProduct

N‐Heterocyclic Carbene Catalyzed Asymmetric Synthesis of Pentacyclic Spirooxindoles via [3+3] Annulations of Isatin‐Derived Enals and Cyclic N‐Sulfon…

2019

Sulfonylchemistry.chemical_classificationkemiallinen synteesiIsatinasymmetric synthesisEnantioselective synthesisGeneral Chemistrycyclic ketiminesMedicinal chemistryCatalysischemistry.chemical_compoundisatin-derived enalschemistryN-heterocyclic carbenesta116pentacyclic spirooxindolesCarbeneorgaaniset yhdisteetAdvanced Synthesis & Catalysis
researchProduct

Discovering Copper for Methane C–H Bond Functionalization

2015

The copper complex Tp(CF3)2,BrCu(NCMe) (1, Tp(CF3)2,Br = hydrotris((3,5-bis(trifluoromethyl)-4-bromo)-pyrazol-1-yl)borate) catalyzes the insertion of the CHCO2Et group (from ethyl diazoacetate N2CHCO2Et, EDA) into the C–H bonds of methane, in a homogeneous process that uses supercritical carbon dioxide (scCO2) as the reaction medium. Other light alkanes such as ethane, propane, and butane have been also functionalized with this copper-based catalyst, in the first example of the derivatization of the series of C1–C4 alkanes with this metal and a soluble catalyst.

Supercritical carbon dioxideTrifluoromethylchemistry.chemical_elementButaneGeneral ChemistryMedicinal chemistryCopperCatalysisMethaneCatalysischemistry.chemical_compoundchemistryEthyl diazoacetatePropaneOrganic chemistryACS Catalysis
researchProduct

Catalytic and anticancer activities of sawhorse-type diruthenium tetracarbonyl complexes derived from fluorinated fatty acids

2013

The reaction of fluorinated fatty acids, perfluorobutyric acid (C3F7CO2H), and perfluorododecanoic acid (C11F23CO2H), with dodecacarbonyltriruthenium (Ru3(CO)12) under reflux in tetrahydrofuran, followed by addition of two-electron donors (L) such as pyridine, 1,3,5-triaza-7-phosphatricyclo[3.3.1.1]decane, or triphenylphosphine, gives stable diruthenium complexes Ru2(CO)4(μ2-η2-O2CC3F7)2(L)2 (1a, L = C5H5N; 1b, L = PTA; 1c, L = PPh3) and Ru2(CO)4(μ2-η2-O2CC11F23)2(L)2 (2a, L = C5H5N; 2b, L = PTA; 2c, L = PPh3). The catalytic activity of the complexes for hydrogenation of styrene under supercritical carbon dioxide has been assessed and compared to the analogous triphenylphosphine complexes w…

Supercritical carbon dioxidechemistry.chemical_elementDecaneMedicinal chemistryRutheniumCatalysisStyrenechemistry.chemical_compoundchemistryPyridineMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryTriphenylphosphineTetrahydrofuranJournal of Coordination Chemistry
researchProduct

Surface and volume non-invasive methods for the structural monitoring of the bass-relief ‘Madonna con Bambino’ (Gorizia, Northern Italy)

2016

Structural analysis of marble statues, carried out by non-invasive and in situ methods, is crucial to define the state of conservation of the artworks and to identify the deterioration phenomena that can affect them. In this work, we combined in situ non-destructive techniques, ultrasonic tomography (US), ultraviolet-induced visible fluorescence (UV-IF) and X-ray fluorescence (XRF) to study the bass-relief ‘Madonna con Bambino’ (Gorizia, Italy). The US revealed the presence of some metallic pivots, associated with areas of high sound velocity; moreover, a more degraded area has been identified in the lower part of the bass-relief. The acquired UV-IF image confirmed the presence of surface d…

Surface Propertiesultrasonic tomographyMineralogySculpturePlant Science01 natural sciencesBiochemistryFluorescenceCalcium CarbonateAnalytical ChemistryPlant scienceMethodsUV-IF010405 organic chemistryChemistrymarbleNon invasiveOrganic Chemistry0104 chemical sciencesNorthern italy010404 medicinal & biomolecular chemistryItalyNon-invasive methodUltrasonic TomographyInorganic materialsdeterioration phenomenaArtStructural monitoring
researchProduct

Cytotoxicity and inhibition of P-glycoprotein by selected medicinal plants from Thailand.

2014

Abstract Ethnopharmacological relevance Thai medicine has a long tradition of tonifying medicinal plants. In the present investigation, we studied the flower extracts of Jasminum sambac, Mammea siamensis, Mesua ferrea, Michelia alba, Mimusops elengi, and Nelumbo nucifera and speculated that these plants might influence metabolism and substance flow in the body. Materials and methods Isolation of porcine brain capillary endothelial cells (PBCECs) as well as multidrug-resistance CEM/ADR5000 leukemia cells, MDA-M;B-231 breast cancer, U-251 brain tumor, and HCT-116 colon cancer cells were used. The calcein-acetoxymethylester (AM) assay was used to measure inhibition of P-glycoprotein transport.…

SwineMesua ferreaMimusops elengiFlowersPharmacologyBlood–brain barrierchemistry.chemical_compoundCell Line TumorNeoplasmsDrug DiscoverymedicineAnimalsHumansATP Binding Cassette Transporter Subfamily B Member 1CytotoxicityP-glycoproteinPharmacologyMedicine East Asian TraditionalPlants MedicinalbiologyTraditional medicinePlant ExtractsMammeaBrainEndothelial Cellsmedicine.diseasebiology.organism_classificationThailandAntineoplastic Agents PhytogenicDrug Resistance MultipleLeukemiamedicine.anatomical_structurechemistryBlood-Brain BarrierDrug Resistance Neoplasmbiology.proteinEndothelium VascularGrowth inhibitionJournal of ethnopharmacology
researchProduct

Induction of apoptosis in a leukemia cell line by triterpene saponins from Albizia adianthifolia

2004

Abstract Triterpenoid saponins, which are present in plants and some marine animals, exert various important pharmacological effects. The present study examines the effects of adianthifoliosides A, B, and D (AdA, AdB, and AdD) together with two prosapogenins (Pro1 and Pro2) obtained from Albizia adianthifolia (Mimosaceae) on human leukemia T-cells (Jurkat cells) and on splenocytes. AdA, AdB, and AdD were found to exhibit a cytotoxic effect on Jurkat cells, whereas the prosapogenins were found to exert a lymphoproliferative effect on this cell type. Furthermore, all tested compounds were found to exert a synergistic lymphoproliferative activity with concanavalin A (ConA) on splenocytes. The …

T-LymphocytesClinical BiochemistryPharmaceutical ScienceAlbizziaApoptosisHemolysisBiochemistryJurkat cellsCell LineJurkat Cellschemistry.chemical_compoundDrug DiscoveryTumor Cells CulturedHumansCytotoxic T cellPropidium iodideOleanolic AcidCytotoxicityMolecular BiologyPlants MedicinalDose-Response Relationship DrugbiologyChemistryOrganic ChemistryBiological activitySaponinsbiology.organism_classificationAntineoplastic Agents PhytogenicTriterpenesBiochemistryConcanavalin ACell culturebiology.proteinMolecular MedicineAlbizia adianthifoliaBioorganic & Medicinal Chemistry
researchProduct