Search results for "HeLa"

showing 10 items of 738 documents

[2,6-Bis(di-tert-butylphosphinomethyl)phenyl-κ3P,C1,P′](trifluoroacetato)palladium(II)

2010

The Pd(II) atom in the title compound, [Pd(C(2)F(3)O(2))(C(24)H(43)P(2))], adopts a distorted square-planar geometry with the P atoms in a trans arrangement, forming two five-membered chelate rings. Four intra-molecular C-H⋯O hydrogen bonds occur. The crystal packing reveals one weak inter-molecular C-H⋯O hydrogen bond, which self-assembles the mol-ecules into infinite chains parallel to the b axis.

Metal-Organic PapersChemistryHydrogen bondchemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsBioinformaticspalladium ; pincer complexes ; hydrogen bonding ; X-ray structureCrystalCrystallographyAtomGeneral Materials ScienceChelationPalladiumActa Crystallographica Section E Structure Reports Online
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{2-[2,2-Bis(4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl- κN)propyl]pyridine}dichloridoiron(II)

2013

The title compound,[FeCl2(C18H25N3O2)], has a distorted tetra-hedral Cl2N2 coordination of the Fe(II) atom as a result of the constraints imposed by the 2-[2,2-bis-(4,4-dimethyl-4,5-di-hydro-1,3-oxazol-2-yl)prop-yl]pyridine ligand. The pyridine ring is almost perpendicular to the six-membered chelated ring containing the metal atom [dihedral angle between their mean planes = 88.5 (1)°].

Metal-Organic PapersGeneral ChemistryDihedral angleCondensed Matter PhysicsRing (chemistry)BioinformaticsMedicinal chemistryPyridine ligandMetalchemistry.chemical_compoundchemistryvisual_artPyridinevisual_art.visual_art_mediumGeneral Materials ScienceChelation
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Bis(cyclohexylammonium) tetrachlorido(oxalato)stannate(IV)

2013

The title salt, (C6H14N)2[Sn(C2O4)Cl4], was obtained as a by-product from the reaction between 2C6H14N+·C2O42−·1.5H2O and SnCl2·2H2O. The cyclohexylammonium cation has a chair conformation. The complex anion consists of an oxalate anion chelating the SnCl4 moiety, resulting in a distorted octahedral coordination sphere of the SnIV atom with the O atoms in equatorial cis positions. In the crystal, cations and anions are linked through N—H...O and N—H...Cl interactions into a layered arrangement parallel to (100).

Metal-Organic Paperschemistry.chemical_classificationCoordination sphereStannatebiologyCyclohexane conformationSalt (chemistry)General ChemistryCondensed Matter Physicsbiology.organism_classificationMedicinal chemistrylcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999TetraMoietyGeneral Materials ScienceAmmoniumChelationActa Crystallographica Section E
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Preparation and reactivity of 1,2-bis(imino)ethylpalladium(II) complexes

1982

Abstract The 1,2-bis(imino)ethylpalladium complex, t r a n s − [ P d C I { C ( = N R ) ︹ C H = N R } ( P P h 3 ) 2 ] (R =p-C6H4OMe, DABI) can be prepared by treatment of [Pd(PPh3)4] with two equivalents of CNC6H4OMe-p followed by slow addition of HCl at −70° C. The σ-bonded 1,2-bis(imino) group can be easily monoprotonated and undergoes acid hydrolysis to give the α-aldehydoimidoyl derivative t r a n s − [ P d C I { C ( = N R ) ︹ C H = O } ( P P h 3 ) 2 ] . Condensation of the aldehydic carbonyl group with methylamine yields the product t r a n s − [ P d C I { C ( = N C 6 H 4 O M e − p ) ︹ C H = N M e } ( P P h 3 ) 2 ] , DABII, with different substituents on the N-imino atoms. Substitution …

MethylamineStereochemistryOrganic ChemistryCenter (category theory)chemistry.chemical_elementBiochemistryAdductInorganic ChemistryMetalchemistry.chemical_compoundchemistryvisual_artMaterials Chemistryvisual_art.visual_art_mediumReactivity (chemistry)ChelationEthyl groupPhysical and Theoretical ChemistryPalladiumJournal of Organometallic Chemistry
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Inhibition of O6-Methylguanine-DNA Methyltransferase by Glucose-Conjugated Inhibitors: Comparison with Nonconjugated Inhibitors and Effect on Fotemus…

2004

The DNA repair protein O(6)-methylguanine-DNA methyltransferase (MGMT) is an important suicide enzyme involved in the defense against O(6)-alkylating mutagens. It also plays a role in the resistance of tumors to anticancer drugs targeting the O(6)-position of guanine, such as temozolomide and fotemustine. Several potent MGMT inhibitors have been developed sensitizing cells to O(6)-alkylating agents. Aimed at targeting MGMT inhibitors to tumor cells, we synthesized MGMT inhibitory compounds conjugated with glucose to improve uptake in tumor cells. Here, we compared O(6)-benzylguanine, O(6)-2-fluoropyridinylmethylguanine (O(6)FPG), O(6)-3-iodobenzylguanine, O(6)-4-bromothenylguanine, and O(6)…

MethyltransferaseGuanineAntineoplastic AgentsPharmacologyBiologyDNA methyltransferaseNitrosourea CompoundsO(6)-Methylguanine-DNA Methyltransferasechemistry.chemical_compoundOrganophosphorus CompoundsIn vivoTemozolomidemedicineHumansEnzyme InhibitorsneoplasmsPharmacologychemistry.chemical_classificationTemozolomideCell Deathdigestive system diseasesIn vitroDacarbazineGlucoseEnzymeBiochemistrychemistryMolecular MedicineFotemustineHeLa Cellsmedicine.drugJournal of Pharmacology and Experimental Therapeutics
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Michelangelon veistämisen muotokielen yhtäläisyyksistä eri mediumeissa - taiteenala mediumina

2007

Michelangelo Buonarrotimediumtilamuotoveisto
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Il Carteggio di Michelangelo. Una biografia attraverso le lettere.

2014

MichelangeloCarteggioSettore L-FIL-LET/10 - Letteratura ItalianaEpistolarioBuonarroti
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Virus-receptor interactions of coxsackie B viruses and their putative influence on cardiotropism

2003

Specific virus-receptor interactions are important determinants in the pathogenesis of viral infections, influencing the location and initiation of primary infection as well as the viral spread to other target organs in the postviremic phase. Coxsackieviruses of group B (CVB) specifically interact with at least two receptor proteins, the coxsackievirus-adenovirus receptor (CAR) and the decay-accelerating factor (DAF), and cause a broad spectrum of diseases, including acute and chronic myocarditis. In the human heart, CAR is predominantly expressed in intercalated discs, regions of utmost importance for the functional integrity of the heart. Since DAF is abundantly expressed in epithelial an…

Microbiology (medical)Coxsackie and Adenovirus Receptor-Like Membrane ProteinvirusesImmunologyCoxsackievirusmedicine.disease_causeVirusViral entryEnterovirus InfectionsmedicineHumansImmunology and AllergyReceptorDecay-accelerating factorCD55 AntigensbiologyMyocardiumVirus receptorGeneral Medicinebiology.organism_classificationVirologyEnterovirus B HumanAdenoviridaeMyocarditisReceptors VirusEnterovirusHeLa CellsMedical Microbiology and Immunology
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Specific DNA probes to detect Escherichia coli strains producing cytotoxic necrotising factor type 1 or type 2

1994

Cytotoxic necrotising factors type 1 (CNF1) and type 2 (CNF2) are produced by many Escherichia coli strains isolated from man and animals with intestinal or extra-intestinal colibacillosis. In most laboratories, CNF-producing strains are detected by a cell cytotoxicity assay and confirmed with a neutralisation assay or a mouse footpad assay. In this study, we sought to determine whether DNA probes could detect clinical isolates of E. coli producing CNF2 or CNF1, or both, without the need for cell cultures or animal assays. Two internal fragments of the gene encoding CNF2 were used as DNA probes: a 875-bp XhoI-PstI DNA fragment and an adjacent 335-bp PstI-ClaI fragment. A positive response w…

Microbiology (medical)DNA BacterialDiarrhea[SDV]Life Sciences [q-bio]Bacterial ToxinsRestriction MappingSEQUENCE GENIQUEmedicine.disease_causeMicrobiologyMicrobiologychemistry.chemical_compoundNucleic acid thermodynamicsRestriction mapmedicineEscherichia coliAnimalsHumansSONDE D'ADNEscherichia coliGeneVero CellsEscherichia coli InfectionsbiologyCytotoxinsHybridization probeEscherichia coli ProteinsNucleic Acid HybridizationGeneral Medicinebiology.organism_classificationEnterobacteriaceaeMolecular biology[SDV] Life Sciences [q-bio]chemistryGenes BacterialFACTEUR CYTOTOXIQUE NECROSANTAutoradiographyMolecular probeDNA ProbesDNAHeLa Cells
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Biological Profiling of Semisynthetic C19-Functionalized Ferruginol and Sugiol Analogues

2021

[EN] The abietane-type diterpenoids are significant bioactive compounds exhibiting a varied range of pharmacological properties. In this study, the first synthesis and biological investigation of the new abietane-diterpenoid (+)-4-epi-liquiditerpenoid acid (8a) together with several of its analogs are reported. The compounds were generated from the readily available methyl callitrisate (7), which was obtained from callitrisic acid present in Moroccan Sandarac resin. A biological evaluation was conducted to determine the effects of the different functional groups present in these molecules, providing basic structure-activity relationship (SAR) elements. In particular, the ferruginol and sugi…

Microbiology (medical)Pharmacology.KetoneStereochemistryCarboxylic acidFarmacología.Antiproliferative activity01 natural sciencesBiochemistryMicrobiologyArticleAntimalarial activityHeLachemistry.chemical_compoundDiterpenoidMoiety03.- Garantizar una vida saludable y promover el bienestar para todos y todas en todas las edadesPharmacology (medical)General Pharmacology Toxicology and PharmaceuticsAbietanechemistry.chemical_classificationMalaria - Chemotherapy.biology010405 organic chemistryChemistrylcsh:RM1-950Sandaracbiology.organism_classificationGABA<sub>A</sub> receptor modulatorsTerpenoidCallitrisic acid0104 chemical sciencesFerruginol010404 medicinal & biomolecular chemistrylcsh:Therapeutics. PharmacologyInfectious DiseasesPaludismo - Farmacoterapia.AbietaneGABAA receptor modulators
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