Search results for "PYRAZOL"

showing 10 items of 720 documents

CCDC 651664: Experimental Crystal Structure Determination

2007

Related Article: J.S.Costa, K.Lappalainen, G.de Ruiter, M.Quesada, Jinkui Tang, I.Mutikainen, U.Turpeinen, C.M.Grunert, P.Gutlich, H.Z.Lazar, J.-F.Letard, P.Gamez, J.Reedijk|2007|Inorg.Chem.|46|4079|doi:10.1021/ic0624017

Space GroupCrystallographytrans-bis(Dicyanamide)-(66'-bis(35-dimethyl-N-pyrazolylmethyl)-22'-bipyridine-NN'N''N''')-iron(ii)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 651667: Experimental Crystal Structure Determination

2007

Related Article: J.S.Costa, K.Lappalainen, G.de Ruiter, M.Quesada, Jinkui Tang, I.Mutikainen, U.Turpeinen, C.M.Grunert, P.Gutlich, H.Z.Lazar, J.-F.Letard, P.Gamez, J.Reedijk|2007|Inorg.Chem.|46|4079|doi:10.1021/ic0624017

Space GroupCrystallographytrans-bis(Methanol)-(66'-bis(35-dimethyl-N-pyrazolylmethyl)-22'-bipyridine-NN'N''N''')-iron(ii) bis(tetrafluoroborate)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 824722: Experimental Crystal Structure Determination

2012

Related Article: L.Lopez-Banet, M.D.Santana, G.Garcia, J.Perez, L.Garcia, L.Lezama, M.Liu|2012|Polyhedron|31|575|doi:10.1016/j.poly.2011.10.014

Space GroupCrystallographytriaqua-(hydrogen tris(35-dimethyl-1H-pyrazol-1-yl)borate)-nickel(ii) dibutyl phosphate hemihydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1942681: Experimental Crystal Structure Determination

2019

Related Article: Júlia Mayans, Mercé Font-Bardia, Albert Escuer|2019|Dalton Trans.|48|16158|doi:10.1039/C9DT03600H

Space GroupCrystallographytriethylammonium lithium tris(mu-hydroxybis(pyridin-2-yl)methanolato)-(mu-carbonato)-tris(mu-pyrazolato)-hexakis(mu-azido)-hexa-nickel(ii) hydrate unknown solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 182938: Experimental Crystal Structure Determination

2003

Related Article: R.Lescouezec, J.Vaissermann, F.Lloret, M.Julve, M.Verdaguer|2002|Inorg.Chem.|41|5943|doi:10.1021/ic020374o

Space GroupCrystallographytris(mu~2~-Cyano)-triaqua-hexacyano-tris(hydrogen tris(pyrazol-1-yl)borate)-tetra-iron(iii) hexahydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Syntheses, X-ray structures, and physicochemical properties of phenoxo-bridged dinuclear nickel(II) complexes: kinetics of transesterification of 2-h…

2009

Four dinuclear nickel(II) complexes [Ni(II)(2)(L(1))(O(2)CMe)(2)(H(2)O)(2)][PF(6)].MeOH.3H(2)O (1), [Ni(II)(2)(L(1))(O(2)CMe)(2)(NCS)] (2), [Ni(II)(2)(L(2))(O(2)CMe)(2)(MeOH)(H(2)O)][ClO(4)] (3), and [Ni(II)(2)(L(2))(O(2)CMe)(2)(MeOH)(H(2)O)][BPh(4)].3MeOH.H(2)O (4) have been synthesized [HL(1): 2,6-bis[N-methyl-N-(2-pyridylethyl)amino]-4-methylphenol; HL(2): 2,6-bis[3-(pyridin-2-yl)pyrazol-1-ylmethyl]-4-methylphenol]. Complexes 1, 3, and 4 are new while complex 2 was reported previously by Fenton and co-workers (the structure of 2 was presented but no physicochemical properties of this complex were reported; in this work such studies have been completed). X-ray crystallographic analyses of…

Spectrophotometry InfraredStereochemistryKineticschemistry.chemical_elementPyrazoleCrystallography X-RayMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundMagneticsOrganophosphorus CompoundsBiomimeticsNickelOrganometallic CompoundsMoietyChelationPhysical and Theoretical ChemistryEsterificationHydrolysisX-rayTitrimetryEstersTransesterificationHydrogen-Ion ConcentrationOrganophosphatesNickelKineticschemistryPotentiometryEthylamineOxidation-ReductionInorganic chemistry
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Substituent effects on the spin equilibrium in iron(II) pyrazolylborate complexes

1995

Abstract Two new complexes of the iron(II) pyrazolylborate system, [Fe(HB(pz)(dmpz) 2 ) 2 ] and [Fe(HB(pz) 2 (dmpz)) 2 ] (pz = pyrazole, dmpz = 3,5-dimethylpyrazole), have been prepared and found to exhibit thermal spin crossover in toluene solutions by means of optical spectroscopy and magnetic susceptibility measurements. Comparison with the published magnetic behaviour of the complexes [Fe(HB(dmpz) 3 ) 2 ] and [Fe(HB(pz) 3 ) 2 ] shows that the high spin state is stabilized with an increasing number of methyl substituents.

Spin statesInorganic chemistrySubstituentPyrazoleTolueneMagnetic susceptibilityInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrySpin crossoverMaterials ChemistryPhysical and Theoretical ChemistrySpin (physics)SpectroscopyInorganica Chimica Acta
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4-Diazopyrazole Derivatives as Potential New Antibiofilm Agents

2008

<i>Background:</i> The recognition that chronic infections and infections associated with medical devices are biofilm related has been the impulse for investigating the antibiofilm properties of some diazopyrazoles biologically active as antimicrobials. <i>Methods:</i> The susceptibility of staphylococcal biofilms was determined at concentrations ranging from 25 to 1.5 µg/ml using crystal violet and methylthiazotetrazolium (MTT) staining. In the case of <i>Candida albicans,</i> we first assessed the anti-germ tube formation effect of 4-NO<sub>2</sub> (compound 1c) and then we evaluated its antibiofilm activity at concentrations ranging from 10…

StaphylococcusGerm tubeMicrobiologychemistry.chemical_compoundCandida albicansDrug DiscoveryPharmacology (medical)Crystal violetCandida albicansPharmacologyTube formationAza CompoundsMolecular StructurebiologyStaphylococcus biofilms Candida Albicans biofilms Antibiofilms activity DiazopyrazolesBiofilmBiological activityGeneral Medicinebiology.organism_classificationAntimicrobialSettore CHIM/08 - Chimica FarmaceuticaCorpus albicansInfectious DiseasesOncologychemistryBiofilmsPyrazoles
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Synthesis and in vitro antileukemic activity of new 4-triazenopyrazole derivatives

2003

Several new 4-(3,3-dimethyltriazeno)-5-benzamidopyrazole derivatives were prepared by reacting 4-diazo-5-benzamidopyrazole derivatives with dimethylamine. The compounds were tested at 10 microM for their vitro antileukemic activity against K562 (Human chronic myelogenous leukemia) and Raji (human Burkitt limphoma ) cell lines. Dacarbazine and methotrexate were used for comparative purpose. The 3-methyl-4-(3,3-dimethyltriazeno)-5-(substituted benzamido)pyrazoles, bearing the pyrazole nucleus free at 1 position, resulted more active than the 1-(substituted phenyl)-3-methyl-4-(3,3-dimethyltriazeno)-5-benzamidopyrazoles. Dacarbazine at 10 microM showed no activity in the above tests. The observ…

StereochemistryDacarbazinePharmaceutical ScienceAntineoplastic AgentsPyrazoleSettore BIO/19 - Microbiologia GeneraleInhibitory Concentration 50Structure-Activity Relationshipchemistry.chemical_compoundCytochrome P-450 Enzyme SystemCell Line TumorLeukemia Myelogenous Chronic BCR-ABL PositiveDrug DiscoverymedicineHumansDimethylamine4-Triazenopyrazoles Antiproliferative activity In vitro antileukemic acitivityDemethylationTriazinesGeneral MedicineBurkitt LymphomaSettore CHIM/08 - Chimica FarmaceuticaIn vitroRaji cellchemistryMechanism of actionPyrazolesGrowth inhibitionmedicine.symptommedicine.drugIl Farmaco
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New complex polycyclic compounds: Synthesis, antiproliferative activity and mechanism of action

2020

Abstract Polycyclic or O-glycoconiugate polycyclic compounds 1a-g were previously tested for their in vitro antiproliferative activity. In this series of compounds, activity increases as log P decreases. Specifically, compounds 1d and 1g showed lower log P values together with the best antiproliferative profiles. With the aim of extending our understanding of the structure–activity relationship (SAR) of this class of compounds, we prepared new polycyclic derivatives 2a-c, which bear on each of the two phenyl rings hydrophilic substituents (OH, SO2NH2 or NHCOCH3). These substituents are able to form hydrogen bonds and to decrease the partition coefficient value as compared with compound 1d. …

StereochemistryO-glycoconjugate polycyclic compoundsApoptosisAntiproliferative activityCrystallography X-Ray01 natural sciencesBiochemistryStructure-Activity RelationshipBreast cancer cell lineCell Line TumorDrug DiscoverymedicineAutophagyMDA-MB231 breast cancer cellsHumansPolycyclic CompoundsCytotoxicityMolecular BiologyCell Proliferation010405 organic chemistryHydrogen bondChemistryOrganic ChemistryHydrogen BondingIn vitro0104 chemical sciencesPartition coefficient010404 medicinal & biomolecular chemistryMechanism of actionApoptosisPyrazolo[34-b]pyrazolo[3′4′:23]azepino[45-f]azocinemedicine.symptom
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