Search results for "ZINC"

showing 10 items of 1081 documents

CCDC 1916086: Experimental Crystal Structure Determination

2019

Related Article: María Cabrero-Antonino, Sonia Remiro-Buenamañana, Manuel Souto, Antonio A. García-Valdivia, Duane Choquesillo-Lazarte, Sergio Navalón, Antonio Rodríguez-Diéguez, Guillermo Mínguez Espallargas, Hermenegildo García|2019|Chem.Commun.|55|10932|doi:10.1039/C9CC04446A

catena-[bis(mu-1H-benzotriazolato-5-carboxylato)-bis(mu-hydroxo)-tri-zinc(ii) NN-dimethylformamide solvate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1916083: Experimental Crystal Structure Determination

2019

Related Article: María Cabrero-Antonino, Sonia Remiro-Buenamañana, Manuel Souto, Antonio A. García-Valdivia, Duane Choquesillo-Lazarte, Sergio Navalón, Antonio Rodríguez-Diéguez, Guillermo Mínguez Espallargas, Hermenegildo García|2019|Chem.Commun.|55|10932|doi:10.1039/C9CC04446A

catena-[bis(mu-1H-benzotriazolato-5-carboxylato)-bis(mu-hydroxo)-tri-zinc(ii) NN-dimethylformamide solvate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 910392: Experimental Crystal Structure Determination

2013

Related Article: Y.Inokuma,S.Yoshioka,J.Ariyoshi,T.Arai,Y.Hitora,K.Takada,S.Matsunaga,K.Rissanen,M.Fujita|2013|Nature (London)|495|461|doi:10.1038/nature11990

catena-[bis(mu~3~-246-tris(Pyridin-4-yl)-135-triazine)-hexakis(iodo)-tri-zinc(ii) 2-(34-dimethoxyphenyl)-35678-pentamethoxy-4H-chromen-4-one clathrate unknown solvate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 910391: Experimental Crystal Structure Determination

2013

Related Article: Y.Inokuma,S.Yoshioka,J.Ariyoshi,T.Arai,Y.Hitora,K.Takada,S.Matsunaga,K.Rissanen,M.Fujita|2013|Nature (London)|495|461|doi:10.1038/nature11990

catena-[bis(mu~3~-246-tris(Pyridin-4-yl)-135-triazine)-hexakis(iodo)-tri-zinc(ii) hemikis(2-(34-dimethoxyphenyl)-5678-tetramethoxy-4H-chromen-4-one) clathrate unknown solvate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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The Status of EGFR Modulates the Effect of miRNA-200c on ZEB1 Expression and Cell Migration in Glioblastoma Cells

2020

Migration of glioblastoma cells into surrounding tissue is one of the main features that makes this tumor incurable. We evaluated whole-genome miRNA expression profiling associated with different EGFR amplification patterns in 30 cases of primary glioblastoma. From the 64 miRNAs that showed differential expression between tumors with a high level of EGFR amplification and tumors without EGFR amplification, 40% were related with cell migration, being miR-200c the most differentially expressed between these two groups. We investigated the effect of miR-200c on ZEB1 expression and cell migration in an in vitro transfection model with a miR-200c mimic, a miR-200c inhibitor and siRNA targeting E…

cell migrationEGFR AmplificationApoptosisBiologyArticleCatalysismiR-200clcsh:ChemistryInorganic ChemistryDownregulation and upregulationCell MovementmicroRNABiomarkers TumorTumor Cells CulturedmedicineZEB1HumansGene silencingEGFR amplificationPhysical and Theoretical Chemistrylcsh:QH301-705.5Molecular BiologySpectroscopyCell ProliferationOrganic ChemistryglioblastomaGene AmplificationZinc Finger E-box-Binding Homeobox 1Cell migrationGeneral MedicineTransfectionPrognosismedicine.diseaseComputer Science ApplicationsErbB ReceptorsGene Expression Regulation NeoplasticMicroRNAslcsh:Biology (General)lcsh:QD1-999Cell cultureMutationCancer researchGlioblastomaInternational Journal of Molecular Sciences
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ChemInform Abstract: New Porphycene Ligands: Octaethyl- and Etioporphycene (OEPc and EtioPc) - Tetra- and Pentacoordinated Zinc Complexes of OEPc.

2010

chemistrybiologychemistry.chemical_elementTetraGeneral MedicineZincbiology.organism_classificationMedicinal chemistryPyrrole derivativesChemInform
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Dialysability of Calcium, Iron, and Zinc in Beans, Chick Peas, and Lentils

2002

chemistrylawchemistry.chemical_elementZincCalciumAtomic absorption spectroscopyNuclear chemistrylaw.invention
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Enantioselective addition of Et2Zn to seven‐membered cyclic imines catalyzed by a (R)-VAPOL-Zn(II) complex

2017

Various substituted dibenzo[b,f][1,4]oxazepines underwent an enantioselective alkylation with Et2Zn catalyzed by a (R)-VAPOL-Zn(II) complex. The corresponding chiral 11-ethyl-10,11-dihydrodibenzo[b,f][1,4]oxazepine derivatives were obtained with good yields and moderate enantioselectivities. This represents the first example of enantioselective addition of Et2Zn to cyclic aldimines.

chemistry.chemical_classificationAldimine010405 organic chemistryChemistryStereochemistryOrganic ChemistryEnantioselective synthesischemistry.chemical_elementZincAlkylation010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesCatalysischemistry.chemical_compoundCatàlisiDrug DiscoveryOxazepineQuímica orgànicaTetrahedron Letters
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ChemInform Abstract: Enantioselective Addition of Terminal Alkynes to N-(Diphenylphosphinoyl)imines Catalyzed by Zn-BINOL Complexes.

2012

Abstract Chiral nonracemic N-(diphenylphosphinoyl)-protected propargylic amines have been prepared by addition of terminal alkynes to N-(diphenylphosphinoyl)aldimines in the presence of dimethylzinc and 3,3′-dibromo-BINOL as catalyst. The reaction works with a variety of aromatic and heteroaromatic aldimines and with different alkynes, providing the expected products in generally good yields and enantiomeric excesses (up to 96%).

chemistry.chemical_classificationAldimineAddition reactionchemistry.chemical_compoundchemistryDimethylzincEnantioselective synthesisOrganic chemistryGeneral MedicineEnantiomerMedicinal chemistryCatalysisChemInform
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Enantioselective addition of terminal alkynes to N-(diphenylphosphinoyl)imines catalyzed by Zn–BINOL complexes

2012

Abstract Chiral nonracemic N-(diphenylphosphinoyl)-protected propargylic amines have been prepared by addition of terminal alkynes to N-(diphenylphosphinoyl)aldimines in the presence of dimethylzinc and 3,3′-dibromo-BINOL as catalyst. The reaction works with a variety of aromatic and heteroaromatic aldimines and with different alkynes, providing the expected products in generally good yields and enantiomeric excesses (up to 96%).

chemistry.chemical_classificationAldiminechemistry.chemical_compoundchemistryOrganic ChemistryDrug DiscoveryDimethylzincEnantioselective synthesisEnantiomerBiochemistryMedicinal chemistryCatalysisTetrahedron
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