Search results for "Triazole"

showing 10 items of 347 documents

CCDC 293619: Experimental Crystal Structure Determination

2007

Related Article: E.Aznar, S.Ferrer, J.Borras, F.Lloret, M.Liu-Gonzalez, H.Rodriguez-Prieto, S.Garcia-Granda|2006|Eur.J.Inorg.Chem.||5115|doi:10.1002/ejic.200600711

bis(mu~2~-Chloro)-tetrakis(mu~2~-35-diamino-124-triazole)-tetraaqua-disulfato-tri-copper(ii) hydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Overcoming Imatinib resistance using CAI, a calcium-mediated signal transduction inhibitor: A new therapeutic strategy for chronic myelogenous leucem…

2008

carboxyamdotriazoleImatinib resistanceChronic Myelogenous Leukemia
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carboxyamidotriazole-orotate inhibits the growth of imatinib resistant chronic myeloid leukaemia cells and modulates exosomes-stimulated angiogenesis

2012

The Bcr/Abl kinase has been targeted for the treatment of chronic myelogenous leukaemia (CML) by imatinib mesylate. Although more common in solid tumors, increased microvessel density was also reported in chronic myelogenous leukaemia and was associated with a significant increase of angiogenic factors, suggesting that vascularity in haematologic malignancies is a controlled process and may play a role in the leukaemogenic process thus representing an alternative therapeutic target. Carboxyamidotriazole-orotate (CTO) is the orotate salt form of carboxyamidotriazole (CAI), an orally bioavailable signal transduction inhibitor that in vitro has been shown to possess antileukaemic activities (1…

carboxyamidotriazole-orotateimatinib resistance
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CCDC 705805: Experimental Crystal Structure Determination

2010

Related Article: G.Dupouy, S.Triki, M.Marchivie, N.Cosquer, C.J.Gomez-Garcia, S.Pillet, E.-E.Bendeif, C.Lecomte, S.Asthana, J.-F.Letard|2010|Inorg.Chem.|49|9358|doi:10.1021/ic101038z

catena-[(mu~2~-2-Dicyanomethylene-1133-tetracyanopropanediide-NN')-bis(4-amino-35-bis(pyridin-2-yl)-124-triazole-NN')-iron(ii)]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 705803: Experimental Crystal Structure Determination

2010

Related Article: G.Dupouy, S.Triki, M.Marchivie, N.Cosquer, C.J.Gomez-Garcia, S.Pillet, E.-E.Bendeif, C.Lecomte, S.Asthana, J.-F.Letard|2010|Inorg.Chem.|49|9358|doi:10.1021/ic101038z

catena-[(mu~2~-2-Dicyanomethylene-1133-tetracyanopropanediide-NN')-bis(4-amino-35-bis(pyridin-2-yl)-124-triazole-NN')-iron(ii)]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 705804: Experimental Crystal Structure Determination

2010

Related Article: G.Dupouy, S.Triki, M.Marchivie, N.Cosquer, C.J.Gomez-Garcia, S.Pillet, E.-E.Bendeif, C.Lecomte, S.Asthana, J.-F.Letard|2010|Inorg.Chem.|49|9358|doi:10.1021/ic101038z

catena-[(mu~2~-2-Dicyanomethylene-1133-tetracyanopropanediide-NN')-bis(4-amino-35-bis(pyridin-2-yl)-124-triazole-NN')-iron(ii)]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Design, Synthesis and Biological Evaluation of Novel Pyrazolo[1,2,4]triazolopyrimidine Derivatives as Potential Anticancer Agents

2021

Three novel pyrazolo-[4,3-e][1,2,4]triazolopyrimidine derivatives (1, 2, and 3) were designed, synthesized, and evaluated for their in vitro biological activity. All three compounds exhibited different levels of cytotoxicity against cervical and breast cancer cell lines. However, compound 1 showed the best antiproliferative activity against all tested tumor cell lines, including HCC1937 and HeLa cells, which express high levels of wild-type epidermal growth factor receptor (EGFR). Western blot analyses demonstrated that compound 1 inhibited the activation of EGFR, protein kinase B (Akt), and extracellular signal-regulated kinase (Erk)1/2 in breast and cervical cancer cells at concentrations…

cervical cancercrystal X-ray analysisPharmaceutical ScienceAntineoplastic AgentsArticleAnalytical ChemistryHeLa03 medical and health sciencesbreast cancerQD241-4410302 clinical medicineDrug DiscoveryHumansEpidermal growth factor receptorPhysical and Theoretical Chemistrypyrazolo[124]triazolopyrimidineCytotoxicityProtein Kinase InhibitorsProtein kinase BCell Proliferation030304 developmental biologyMitogen-Activated Protein Kinase 1pyrazolo[124]triazolopyrimidine; EGF-receptor inhibitor; breast cancer; cervical cancer; molecular docking; crystal X-ray analysis0303 health sciencesBinding SitesMitogen-Activated Protein Kinase 3biologyChemistryKinaseOrganic ChemistryBiological activitymolecular dockingTriazolesbiology.organism_classificationMolecular biologyIn vitroErbB ReceptorsMolecular Docking SimulationPyrimidinesChemistry (miscellaneous)Docking (molecular)030220 oncology & carcinogenesisbiology.proteinMolecular MedicineProto-Oncogene Proteins c-aktEGF-receptor inhibitorHeLa CellsProtein BindingMolecules
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P-Chirogenic Triazole-Based Phosphine: Synthesis, Coordination Chemistry, and Asymmetric Catalysis

2020

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryEnantioselective synthesisTriazole010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCoordination complexchemistry.chemical_compoundchemistryTransition metalPhysical and Theoretical ChemistryPhosphineEuropean Journal of Organic Chemistry
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Synthesis of conformationally restricted 1,2,3-triazole-substituted ethyl β- and γ-aminocyclopentanecarboxylate stereoisomers. Multifunctionalized al…

2010

Abstract Stereoisomers of 1,2,3-triazole-functionalized, conformationally restricted β- or γ-amino esters with a cyclopentane skeleton were efficiently synthetized from the bicyclic β-lactam 6-azabicyclo[3.2.0]hept-3-en-7-one (1) and Vince γ-lactam (15) in five or six steps involving the azide–alkyne 1,3-dipolar cycloaddition of azido-substituted amino ester stereoisomers with nonsymmetric acetylenes. The azide–alkyne click reactions were investigated under thermal and Cu(I)-catalyzed conditions. Surprisingly, the thermally induced cycloaddition furnished the corresponding 1,4-triazoles regioselectively, which also took place selectively in response to Cu(I) catalysis.

chemistry.chemical_classification123-TriazoleAmino estersBicyclic moleculeStereochemistryOrganic ChemistryBiochemistryChemical synthesisCycloadditionchemistry.chemical_compoundAlicyclic compoundchemistryDrug Discovery13-Dipolar cycloadditionClick chemistryTetrahedron
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Synthesis, crystal structure and magnetic properties of bis[μ-bis(3-(pyridin-2-yl)-1,2,4-triazole-N′,N1,N2)] bis[triaqua nickel(II)] tetranitrate

1998

Abstract A new dinuclear nickel(II) coordination compound of formula Ni2(Hpt)2(H2O)6(NO3)4 (Hpt=3-(pyridin-2-yl)-1,2,4-triazole) was synthesized. The structure was solved at 298 K by single-crystal X-ray analysis. Bisμ-bis(3-(pyridin-2-yl)-1,2,4-triazole-N′,N1,N2) bistriaqua nickel(II) tetranitrate (C14H24N12O18Ni2) crystallizes in the triclinic space group P-1, a=7.2266(1), b=9.9144(1), c=11.2647(1) A, α=66.854(1)°, β=74.000(1)°, γ=86.400(2)°, V=712.42(1) A3, Z=1 (dinuclear units), 2823 reflections (1 > 2σ(I)), R1=0.0442, wR2=0.1197. The Ni(II) ions are bridged by two neutral Hpt ligands coordinating via N1 and N2 in the equatorial plane, Ni(1)-Ni(1)′=4.098(1) A. The Hpt bridging mode is a…

chemistry.chemical_classification124-Triazolechemistry.chemical_elementCrystal structureTriclinic crystal systemCoordination complexInorganic Chemistrychemistry.chemical_compoundNickelCrystallographychemistryOctahedronSuperexchangeMaterials ChemistryMoleculePhysical and Theoretical ChemistryInorganica Chimica Acta
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