Search results for "4-O"

showing 10 items of 457 documents

CCDC 285889: Experimental Crystal Structure Determination

2006

Related Article: B.Frackowiak, K.Ochalik, A.Bialonska, Z.Ciunik, C.Wawrzenczyk, S.Lochynski|2006|Tetrahedron:Asymm.|17|124|doi:10.1016/j.tetasy.2005.11.025

(1S3S7S9R)-(+)-1010-Dimethyl-3-iodomethyl-4-oxatricyclo(7.1.0^19^.0^37^)decan-5-oneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 285890: Experimental Crystal Structure Determination

2006

Related Article: B.Frackowiak, K.Ochalik, A.Bialonska, Z.Ciunik, C.Wawrzenczyk, S.Lochynski|2006|Tetrahedron:Asymm.|17|124|doi:10.1016/j.tetasy.2005.11.025

(1S3S7S9R)-(+)-3-Bromomethyl-1010-dimethyl-4-oxatricyclo(7.1.0^19^.0^37^)decan-5-oneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1952561: Experimental Crystal Structure Determination

2020

Related Article: Gianluca Ambrosi, M. Paz Clares, Isabel Pont, Mauro Formica, Vieri Fusi, Angela Ricci, Paola Paoli, Patrizia Rossi, Enrique García-España, Mario Inclán|2020|Dalton Trans.|49|1897|doi:10.1039/C9DT04764F

(N-{[6-(5-phenyl-134-oxadiazol-2-yl)pyridin-2-yl]methyl}-2-[36915-tetra-azabicyclo[9.3.1]pentadeca-1(15)1113-trien-6-yl]ethan-1-amine)-copper diperchlorateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Unexpected Substituent Effects in the Iso-Heterocyclic Boulton-Katritzky Rearrangement of 3-Aroylamino-5-methyl-1,2,4-oxadiazoles: A Mechanistic Stud…

2019

The kinetics of the iso-heterocyclic mononuclear rearrangement of some 3-aroylamino-5-methyl-1,2,4-ozadiazoles was carefully examined under largely variable acidic or alkaline conditions. This reaction may proceed via two different mechanistic pathways (an uncatalyzed and a base-catalyzed one), as accounted for also by the evaluation of the relevant activation parameters. Substituent effects, as quantified by means of the Hammett’s equation, appear relatively modest; however, they reveal some interesting anomalies, which enabled us to draw a very precise picture of the intimate reaction course.

010304 chemical physicsChemistryKineticsSubstituent124-oxadiazoleSettore CHIM/06 - Chimica OrganicaMononuclear Heterocyclic Rearrangement010402 general chemistry01 natural sciences0104 chemical sciencesKineticschemistry.chemical_compoundSubstituent effectComputational chemistry0103 physical sciencesPhysical and Theoretical ChemistryReaction mechanismThe journal of physical chemistry. A
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Investigation on Quantitative Structure-Activity Relationships of 1,3,4-Oxadiazole Derivatives as Potential Telomerase Inhibitors.

2020

Background:Telomerase, a reverse transcriptase, maintains telomere and chromosomes integrity of dividing cells, while it is inactivated in most somatic cells. In tumor cells, telomerase is highly activated, and works in order to maintain the length of telomeres causing immortality, hence it could be considered as a potential marker to tumorigenesis.A series of 1,3,4-oxadiazole derivatives showed significant broad-spectrum anticancer activity against different cell lines, and demonstrated telomerase inhibition.Methods:This series of 24 N-benzylidene-2-((5-(pyridine-4-yl)-1,3,4-oxadiazol-2yl)thio)acetohydrazide derivatives as telomerase inhibitors has been considered to carry out QSAR studies…

0301 basic medicineModels MolecularTelomeraseQuantitative structure–activity relationship2D descriptorsDatasets as TopicQuantitative Structure-Activity RelationshipAntineoplastic Agents010402 general chemistry01 natural sciencesModels BiologicalAnticancer activityMLR03 medical and health sciencesInhibitory Concentration 50Drug DiscoveryLeast-Squares AnalysisTelomerase134-oxadiazolesOxadiazolesMolecular StructureDrug discoveryChemistryQSARQuantitative structureCombinatorial chemistry0104 chemical sciencesTelomerase inhibitors030104 developmental biology1 3 4 oxadiazole derivativesDrug Screening Assays AntitumorCurrent drug discovery technologies
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CCDC 915397: Experimental Crystal Structure Determination

2013

Related Article: M.Saccone,G.Cavallo,P.Metrangolo,A.Pace,I.Pibiri,T.Pilati,G.Resnati,G.Terraneo|2013|CrystEngComm|15|3102|doi:10.1039/C3CE40268A

112233445566-Dodecafluoro-16-diiodohexane 44'-(124-oxadiazole-35-diyl)dipyridineSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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The synthesis of fluorinated heteroaromatic compounds. Part 1. Five-membered rings with more than two heteroatoms. A review

2005

(2005). THE SYNTHESIS OF FLUORINATED HETEROAROMATIC COMPOUNDS. PART 1. FIVE-MEMBERED RINGS WITH MORE THAN TWO HETEROATOMS. A REVIEW. Organic Preparations and Procedures International: Vol. 37, No. 5, pp. 447-506.

13-DIPOLE ADDITION REACTIONSTETRASULFUR TETRANITRIDEChemistryOrganic ChemistryHeteroatomSUBSTITUTED 123-TRIAZOLES124-OXADIAZOLE SERIESSettore CHIM/06 - Chimica OrganicaORGANIC-CHEMISTRYEXPEDIENT ROUTEUNSATURATED NITROGEN-COMPOUNDSORGANOFLUORINE COMPOUNDSOrganic chemistryN-METHOXYTRIAZOLIUM SALTSHETEROCYCLIC-COMPOUNDS
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CCDC 1046555: Experimental Crystal Structure Determination

2015

Related Article: Agris Be̅rziņš , Edgars Skarbulis , and Andris Actiņš|2015|Cryst.Growth Des.|15|2337|doi:10.1021/acs.cgd.5b00138

1-(1-(4-(4-fluorophenyl)-4-oxobutyl)piperidin-4-yl)-13-dihydro-2H-benzimidazol-2-oneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Synthesis and anti-HIV activity of 2,3-diaryl-1,3-thiazolidin-4-(thi)one derivatives.

2002

Several 2,3-diaryl-1,3-thiazolidine-4-thione derivatives and 2,3-diaryl-1,3-thiazolidin-4-ones bearing a methyl group at C-5 position have been synthesized and tested as anti-HIV agents. The results of the in vitro tests showed that some of them proved to be effective inhibitors of HIV-1 replication.

23-Diaryl-13-thiazolidine-4-thioneAnti-HIV activity23-Diaryl-13-thiazolidin-4-oneStereochemistryAnti-HIV AgentsCell SurvivalPharmaceutical ScienceVirus ReplicationChemical synthesischemistry.chemical_compoundInhibitory Concentration 50Structure-Activity RelationshipThiadiazolesDrug DiscoveryThiadiazolesmedicineTumor Cells CulturedStructure–activity relationshipHumansAnti hiv activityReverse-transcriptase inhibitorGeneral MedicineSettore CHIM/08 - Chimica FarmaceuticaIn vitrochemistryNNRTIsLactamHIV-1EpimerMethyl groupmedicine.drugFarmaco (Societa chimica italiana : 1989)
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CCDC 1481997: Experimental Crystal Structure Determination

2016

Related Article: Fangfang Pan, Ngong Kodiah Beyeh, Robin H. A. Ras, Kari Rissanen|2016|CrystEngComm|18|5724|doi:10.1039/C6CE01229A

281420-tetra-n-propyl-46101216182224-octahydroxy-5111723-tetrakis(cyclohexylammoniomethyl)calix(4)arene tribromide tri-iodide 14-dioxane solvate hydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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