Search results for "Derivative"

showing 10 items of 1074 documents

Biological activity of flucycloxuron, a novel benzoylphenylurea derivative, onTenebrio molitor: comparison with diflubenzuron and triflumuron

1993

Flucycloxuron, a novel benzoylphenylurea (BPU) derivative, exhibited insecticidal activity when injected into newly ecdysed pupae ofTenebrio molitor. Mortality occurs because of defective adult ecdysis. Treatment caused a reduction in both cuticle thickness and incorporation of14C-labelled precursor into chitin, although it had no significant effect on the protein synthesis. The potencies of other BPU compounds as inhibitors of chitin biosynthesis have been examined and results showed that diflubenzuron was less effective than either flucycloxuron or triflumuron.

PharmacologyBenzoylphenylureaCuticlefungiBiological activityCell BiologyBiologyCellular and Molecular Neurosciencechemistry.chemical_compoundDiflubenzuronBiochemistryChitinchemistryEcdysisBotanyProtein biosynthesisMolecular MedicineMolecular BiologyDerivative (chemistry)Experientia
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Comparative Structural Studies of 4-Diazopyrazole Derivatives by X-Ray Diffraction and Theoretical Investigation

2005

The X-Ray crystal and molecular structures of the 4-pyrazol derivatives 3-methyl-4-diazo-5-benzamido-1H-pyrazole (4) and 3-benzamido-5-methyl-1H-pyrazole (3) have been determined. A dimeric structure has been found for the first and polymeric for the second. A comparison of 4 with 1,3-dimethyl-4-diazo-5-benzamido-lH-pyrazole (2) shows differences in the geometrical parameters of the pyrazole ring due to electron delocalization in 2 consequent to the nitrogen negative charge in the latter. Theoretical investigation at the density functional theory (DFT) level shows difference in the molecular electronic distribution of 2 and 4, in agreement with the structural parameters and the IR stretchin…

PharmacologyChemistryOrganic ChemistryElectron delocalizationPyrazoleRing (chemistry)Analytical ChemistryCrystalCrystallographychemistry.chemical_compoundNegative chargeX-ray crystallographyX-Ray crystal molecular structures derivativesDensity functional theory
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Designing fluorous domains. Synthesis of a series of pyridinium salts bearing a perfluoroalkylated azole moiety

2006

The synthesis of a series of N-methylpyridinium salts bearing a perfluoroalkylated 1,2,4-oxadiazole or 1,2,4-triazole moiety is reported. X-Ray structures of representative perfluoroalkyl-triazolylpyridine (15) and methyl- pyridinium iodide salt (5a) are reported. Their crystal packing clearly shows segregation between the aromatic and parallel double layer fluorinated regions.

PharmacologyDouble layer (biology)chemistry.chemical_classificationMELTSCRYSTALChemistryDERIVATIVESPHOTOCHEMISTRYOrganic ChemistryFLUORINATED HETEROCYCLIC-COMPOUNDS124-TriazoleEXPEDIENT ROUTEAnalytical ChemistryCrystalIodide saltchemistry.chemical_compoundLIGHTIONIC LIQUIDSOXADIAZOLEPolymer chemistryMoietyOrganic chemistryAzolePyridiniumPOLYMERS
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The Cytotoxic Properties of Natural Coumarins Isolated from Roots ofFerulago campestris(Apiaceae) and of Synthetic Ester Derivatives of Aegelinol

2009

Grandivittin (1), agasyllin (2), aegelinol benzoate (3) and felamidin (20), four natural coumarins isolated from Ferulago campestris, and several synthetic ester derivatives of aegelinol (4) were tested against four tumor cell lines. Some of them were shown to be marginally cytotoxic against the A549 lung cancer cell line.

PharmacologyEster derivativesfood.ingredientApiaceaeStereochemistryPlant compositionPlant ScienceGeneral MedicineBiologybiology.organism_classificationFerulago campestrisFerulagofoodComplementary and alternative medicineDrug DiscoveryCytotoxic T cellOrganic chemistryNatural Product Communications
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Fluorinated Heterocyclic Compounds. A Photochemical Approach to a Synthesis of Polyfluoroaryl-1,2,4-triazoles.

2005

The reaction of some fluorinated 1,2,4-oxadiazoles in the presence of methylamine or propylamine has been investigated. The irradiation in methanol or acetonitrile leads with acceptable yields to the corresponding fluorinated 1- methyl- or 1-propyl-1,2,4-triazole.

PharmacologyFLUORO HETEROCYCLESMethylamineOrganic ChemistryQUINAZOLIN-4-ONES124-Triazole124-OXADIAZOLESPropylamineSettore CHIM/06 - Chimica OrganicaGeneral MedicineEXPEDIENT ROUTEPhotochemistryMedicinal chemistryAnalytical Chemistrychemistry.chemical_compound124-TRIAZOLESchemistryTriazole derivativesOrganic chemistry5-MEMBERED HETEROCYCLESIrradiationMethanolAcetonitrilePHOTOINDUCED MOLECULAR-REARRANGEMENTSChemInform
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�ber die Wirkung von Strophanthidin-3-bromacetat am Papillarmuskel des Meerschweinchens

1971

In experiments on isolated, electrically stimulated papillary muscles or auricles of guinea pig hearts some characteristics of the inotropic action of strophanthidin-3-bromaocetate (SBA), a derivative of k-strophanthidin which is supposed to be an irreversible inhibitor of the (Na+-K+)-activated ATPase, were studied and compared with the behaviour of k-strophanthidin and digitoxin.

PharmacologyInotropemedicine.medical_specialtybiologyDigitoxinATPasePharmacology toxicologyGeneral MedicineGuinea pigchemistry.chemical_compoundEndocrinologychemistryInternal medicinebiology.proteinmedicineDerivative (chemistry)medicine.drugNaunyn-Schmiedebergs Archiv f�r Pharmakologie
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Posaconazole concentrations in the central nervous system

2008

more susceptible to the killing activity of caspofungin. This study is the first comparing caspofungin killing activity against the closely related species C. parapsilosis, C. orthopsilosis and C. metapsilosis. Killing curves, regardless of the medium used, showed a decreasing order of susceptibility to caspofungin: C. metapsilosis . C. orthopsilosis . C. parapsilosis. Based on high echinocandin MICs for C. parapsilosis sensu stricto, in the case of isolates identified as C. parapsilosis sensu lato low MICs of echinocandins may be regarded as an indicator that an isolate is in fact C. orthopsilosis or C. metapsilosis; in the case of isolates with low echinocandin MICs, DNA-based identificat…

PharmacologyMicrobiology (medical)PosaconazoleEchinocandinBiologyPharmacologybacterial infections and mycosesBiological fluidMicrobiologychemistry.chemical_compoundInfectious Diseaseschemistryparasitic diseasespolycyclic compoundsTriazole derivativesmedicinePharmacology (medical)CaspofunginEchinocandinsSensu strictoSerum chemistrymedicine.drugJournal of Antimicrobial Chemotherapy
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Synthetic derivatives of aromatic abietane diterpenoids and their biological activities

2014

Naturally occurring aromatic abietane diterpenoids (dehydroabietanes) exhibit a wide range of biological activities. A number of synthetic studies aimed at modifying the abietane skeleton in order to obtain new potential chemotherapeutic agents have been reported. In this study, the biological activities of synthetic derivatives of aromatic abietane diterpenoids are reviewed.

PharmacologyMolecular StructureSynthetic derivativesOrganic ChemistryCarnosic acidGeneral MedicineTerpenoidFerruginolchemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryDehydroabietic acidDiterpenesAbietaneEuropean Journal of Medicinal Chemistry
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Ircinal E, a New Manzamine Derivative from the Indonesian Marine Sponge Acanthostrongylophora ingens

2015

Chemical investigation of the MeOH extract of the sponge Acanthostrongylophora ingens afforded the new manzamine derivative ircinal E (1), in addition to six known metabolites (2–7). The structure of the new compound was unequivocally elucidated using one- and two-dimensional NMR spectroscopy, as well as high-resolution mass spectrometry. Compounds 1–6 exhibited strong to moderate cytotoxicity against the murine lymphoma L5178Y cell line with IC50 values ranging from 2.8 to 21.7 μM.

PharmacologyMurine lymphomabiologyStereochemistryAcanthostrongylophora ingensPlant ScienceGeneral MedicineNuclear magnetic resonance spectroscopybiology.organism_classificationMass spectrometrySpongechemistry.chemical_compoundComplementary and alternative medicinechemistryDrug DiscoveryBotanyMoleculeCytotoxicityDerivative (chemistry)Natural Product Communications
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The Chemistry of [1,2,3]Triazolo[1,5- a] pyridines

2003

The reactivity of [1,2,3]triazolo[1,5-a]pyridines 1 is described. Triazolopyridines react with electrophiles in two contrasting ways, giving 3-substituted triazolopyridines 2, or products 3, resulting from triazolo ring opening with loss of molecular nitrogen. The triazolopyridines can be lithiated at -40 degrees C by lithium diisopropylamide in ether giving regiospecifically the 7-lithio derivative. Bromotriazolopyridines have activation towards nucleophilic substitution at position 5 and 7, and benzenoid inertness at position 6. The parent compound 1a is easily hydrogenated giving tetrahydrotriazolopyridine 11a in high yield; when the triazolopyridines have substituents, the hydrogenation…

PharmacologyPhotochemistryPyridinesSubstituentPyridinium CompoundsEtherGeneral MedicineTriazolesRing (chemistry)Lithium diisopropylamidechemistry.chemical_compoundchemistryCyclizationDrug DiscoveryElectrophileSolventsNucleophilic substitutionOrganic chemistryReactivity (chemistry)HydrogenationDerivative (chemistry)Journal of Enzyme Inhibition and Medicinal Chemistry
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