Search results for "Interactions"

showing 10 items of 1963 documents

Infectious Entry Pathway of Enterovirus B Species

2015

Enterovirus B species (EV-B) are responsible for a vast number of mild and serious acute infections. They are also suspected of remaining in the body, where they cause persistent infections contributing to chronic diseases such as type I diabetes. Recent studies of the infectious entry pathway of these viruses revealed remarkable similarities, including non-clathrin entry of large endosomes originating from the plasma membrane invaginations. Many cellular factors regulating the efficient entry have recently been associated with macropinocytic uptake, such as Rac1, serine/threonine p21-activated kinase (Pak1), actin, Na/H exchanger, phospholipace C (PLC) and protein kinase Cα (PKCα). Another…

coxsackievirus A9EchovirusEndosomelcsh:QR1-502Virus AttachmentEndosomesReviewCoxsackievirusEndocytosismedicine.disease_causelcsh:Microbiology03 medical and health sciencesVirologymedicineReceptorProtein kinase A030304 developmental biology0303 health sciencesbiologyKinase030302 biochemistry & molecular biologyechovirusVirus Internalizationbiology.organism_classificationVirologyEndocytosisEnterovirus B Human3. Good healthCell biologyInfectious DiseasesHost-Pathogen InteractionsEnterovirusentrycoxsackievirus B3signalingViruses
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The pion single-event latch-up cross-section enhancement : mechanisms and consequences for accelerator hardness assurance

2021

Pions make up a large part of the hadronic environment typical of accelerator mixed-fields. Characterizing device cross-sections against pions is usually disregarded in favour of tests with protons, whose single-event latch-up cross-section is, nonetheless, experimentally found to be lower than that of pions for all energies below 250 MeV. While Monte-Carlo simulations are capable of reproducing such behavior, the reason of the observed pion cross-section enhancement can only be explained by a deeper analysis of the underlying mechanisms dominating proton-silicon and pion-silicon reactions. The mechanisms dominating the single-event latchup response are found to vary with the energy under c…

cross-sectionprotonitpiiprotonsacceleratorionisoiva säteilyNuclear TheoryneutronshiukkaskiihdyttimetelektroniikkakomponentitFLUKAsäteilyfysiikkaSELradiation hardness assurancenuclear interactionspionsNuclear Experiment
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The subtle balance of weak supramolecular interactions: The hierarchy of halogen and hydrogen bonds in haloanilinium and halopyridinium salts

2010

The series of haloanilinium and halopyridinium salts: 4-IPhNH₃Cl (1), 4-IPhNH₃Br (5), 4-IPhNH₃H₂PO₄ (6), 4-ClPhNH₃H₂PO₄ (8), 3-IPyBnCl (9), 3-IPyHCl (10) and 3-IPyH-5NIPA (3-iodopyridinium 5-nitroisophthalate, 13), where hydrogen or/and halogen bonding represents the most relevant non-covalent interactions, has been prepared and characterized by single crystal X-ray diffraction. This series was further complemented by extracting some relevant crystal structures: 4-BrPhNH3Cl (2, CCDC ref. code TAWRAL), 4-ClPhNH3Cl (3, CURGOL), 4-FPhNH3Cl (4, ANLCLA), 4-BrPhNH3H2PO4, (7, UGISEI), 3-BrPyHCl, (11, CIHBAX) and 3-ClPyHCl, (12, VOQMUJ) from Cambridge Structural Database for sake of comparison. Bas…

crystal engineeringhalogen bondingweak interactionshydrogen bondingsupramolecular chemistry
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Crystal structure of 2-[chloro(4-methoxyphenyl)methyl]-2-(4-methoxyphenyl)-5,5-dimethylcyclohexane-1,3-dione

2016

One of the methyl groups and the 4-meth­oxy­phenyl substituent are in axial positions and the chloro­(4-meth­oxy­phen­yl)methyl substituent is in the equatorial position of the cyclo­hexane ring which adopts a chair conformation. The packing features inversion-symmetric dimeric units and strands along [100] and [010] established by weak C—H⋯O and C—H⋯Cl contacts.

crystal structure010405 organic chemistryStereochemistryCyclohexane conformationSubstituentweak C—H⋯O and C—H⋯Cl inter­actionsGeneral ChemistryCrystal structureMeth-010402 general chemistryCondensed Matter PhysicsRing (chemistry)01 natural sciencesResearch Communications0104 chemical sciencesweak C—H...O and C—H...Cl interactionsHexanelcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999General Materials ScienceActa Crystallographica Section E: Crystallographic Communications
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5-Methylbenzo[d][2,1,3]selenadiazole

2017

In the crystal of the title compound, C7H6N2Se, the molecules are arranged in rods along theb-axis direction and form dimeric units due to intermolecular Se...N contacts of 2.982 (2) Å. The molecules are further linked by weak π–π stacking interactions between the 2,1,3-selenadiazole and six-membered aromatic rings [centroid–centroid distance = 3.8509 (11) Å and ring slippage = 1.539 (3) Å].

crystal structure010405 organic chemistryStereochemistrySe...N contactsStackingselenadiazoleAromaticityCrystal structure010402 general chemistryRing (chemistry)01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundchemistryπ–π interactionslcsh:QD901-999Diazolelcsh:CrystallographyIUCrData
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catena-Poly[[diaquabis[1,4-bis(pyridin-4-yl)buta-1,3-diyne-κN]iron(II)]-μ-cyanido-κ2N:C-[dicyanido-κ2C-platinum(II)]-μ-cyanido-κ2C:N]

2017

The molecular structure of the title compound, [FePt(CN)4(C14H8N2)2(H2O)2]n, consists of one-dimensional polymeric [–Fe–NC–Pt(CN)2–CN–]∞chains. Two water molecules and two monodentate 1,4-bis(pyridin-4-yl)buta-1,3-diyne (bpb) ligand molecules complete the octahedral coordination sphere of the FeIIatoms. The Fe—N(py) bond length (py is pyridine) is 2.2700 (15) Å, Fe—N(cyanide) is 2.1185 (16) Å and the Fe—O distance is 2.1275 (14) Å. The water molecules are hydrogen bonded to either bpb ligands or cyanide groups of the planar [Pt(CN)4]2−anion of adjacent polymeric chains. These O—H...N hydrogen bonds, in conjunction with offset and tilted π–π stacking interactions between bpb ligands and cyan…

crystal structureCoordination sphereDenticityLigandHydrogen bondStereochemistryCyanideCrystal structurebitopic bpb ligandhydrogen bonding010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesBond lengthchemistry.chemical_compoundchemistryπ–π stacking interactionsPyridinelcsh:QD901-999lcsh:CrystallographyIUCrData
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Crystal structure of (1S,3R,8R,9S,10R)-10-bromomethyl-2,2-dichloro-9,10-epoxy-3,7,7-trimethyltricyclo[6.4.0.01,3]dodecane

2015

The title compound, C16H23BrCl2O, was synthesized in three steps from β-himachalene (3,5,5,9-tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzocycloheptene), which was isolated from the essential oil of the Atlas cedar (cedrus atlantica). The molecule is built up from two fused six- and seven-membered rings, each linked to a three-membered ring. The six-membered ring has a screw-boat conformation, whereas the seven-membered ring displays a twist-boat conformation. The absolute structure was established unambiguously from anomalous dispersion effects.

crystal structureCrystallographyChemistryCedrus atlanticaπ–π inter­actionsGeneral ChemistryCrystal structureCondensed Matter PhysicsRing (chemistry)Data Reportslaw.inventionAbsolute structureCrystallographyQD901-999lawπ–π interactionsGeneral Materials Scienceβ-himachalene derivativeEssential oilActa Crystallographica Section E Crystallographic Communications
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Crystal structure of (E)-4-[N-(7-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)carboximido-yl]phenol.

2015

The molecule of the title compound, C21H17N3O, is built up from fused five- and six-membered rings connected to a methyl group, a phenyl ring and an (iminomethyl)phenol group. The fused ring system is almost planar (r.m.s. deviation = 0.031 Å) and forms dihedral angles of 64.97 (7) and 18.52 (6)° with the phenyl ring and the (iminomethyl)phenol group, respectively. In the crystal, centrosymmetric molecules are linked by pairs of C—H...π interactions into dimeric units, which are further connected by O–H...N hydrogen bonds to form layers parallel to (101).

crystal structureCrystallographyHydrogen bondimidazo[12a]pyridine derivativeGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsRing (chemistry)Bioinformaticshydrogen bondingC—H⋯π inter­actionsMedicinal chemistryData ReportsCrystalchemistry.chemical_compoundC—H...π interactionschemistryQD901-999Group (periodic table)PhenolGeneral Materials ScienceMethyl groupActa crystallographica. Section E, Crystallographic communications
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Crystal structure of 2-(adamantan-1-yl)-5-(4-bromophenyl)-1,3,4-oxadiazole

2014

In the title molecule, C18H19BrN2O, the benzene ring is inclined to the oxadiazole ring by 10.44 (8)°. In the crystal, C—H...π interactions link the molecules in a head-to-tail fashion, forming chains extending along thec-axis direction. The chains are further connected by π–π stacking interactions, with centroid–centroid distances of 3.6385 (7) Å, forming layers parallel to thebcplane.

crystal structureCrystallographyStackingπ–π inter­actionsGeneral ChemistryCrystal structureCondensed Matter PhysicsBioinformaticsRing (chemistry)adamntane derivativeData ReportsCrystalchemistry.chemical_compoundCrystallographyC—H...π hydrogen bonds134-oxa­diazoleC—H⋯π hydrogen bondschemistryQD901-999π–π interactions134-oxadiazoleDiazoleGeneral Materials ScienceBenzeneActa Crystallographica Section E
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Crystal structure ofcis-1-phenyl-8-(pyridin-2-ylmethyl)dibenzo[1,2-c:2,1-h]-2,14-dioxa-8-aza-1-borabicyclo[4.4.0]deca-3,8-diene

2017

The present work describes the synthesis and crystal structure of the new B-phenyl­oxaza­borocine, C26H23BN2O2. The title compound adopts a zwitterionic form with a significant intra­molecular N→B dative bond and inter­molecular C—H⋯O inter­actions connecting mol­ecules parallel to the b axis.

crystal structureC—H...O interactionsDieneStereochemistrychemistry.chemical_elementManganeseCrystal structureRelated derivatives010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesResearch Communications//purl.org/becyt/ford/1 [https]CrystalB-phenyldioxazaborocinechemistry.chemical_compoundzwitterionic heterocycleB-PhenyldioxazaborocineN-B Dative Bond//purl.org/becyt/ford/1.4 [https]General Materials ScienceZwitterionic HeterocycleCrystallographyC-Ho InteractionsHydrogen bondChemistryOtras Ciencias QuímicasCiencias QuímicasN—B dative bondGeneral ChemistryCondensed Matter Physics0104 chemical sciencesB-phenyl­dioxaza­borocineC—H⋯O inter­actionsQD901-999Tripodal ligandCrystal StructureCIENCIAS NATURALES Y EXACTASDeca-Acta Crystallographica Section E Crystallographic Communications
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