Search results for "Molecular chemistry"

showing 10 items of 1103 documents

Plant Specialized Metabolites in Hazelnut (Corylus avellana) Kernel and Byproducts: An Update on Chemistry, Biological Activity, and Analytical Aspec…

2019

Abstract Corylus avellana (hazelnut) is one of the most popular tree nuts on a worldwide basis. The main products of C. avellana are kernels, a nutritious food, with a high content of healthy lipids, contained in a hard shell. In recent years, along with the ongoing research carried out on hazelnut kernels, a growing interest has been addressed to the hazelnut byproducts including hazelnut skin, hazelnut hard shell, and hazelnut green leafy cover as well as hazelnut tree leaf. These byproducts deriving from the roasting, cracking, shelling/hulling, and harvesting processes have been found as a source of “phytochemicals” with biological activity. The aim of this review is to provide a compre…

phenolicsPharmaceutical ScienceAntineoplastic Agents01 natural sciencesNutritious foodAnalytical ChemistryHuman healthCorylusAnti-Infective AgentsBetulaceaeDrug Discoveryanalytical tools; Betulaceae; biological activities; Corylus avellana; diarylheptanoids; phenolics; taxanes; Animals; Anti-Infective Agents; Antineoplastic Agents; Antipain; Corylus; Humans; Nuts; Plant ExtractsAnimalsAntipainHumansNutsFood scienceHazelnut treeBeneficial effectsRoastingPharmacology010405 organic chemistryChemistryPlant ExtractsOrganic Chemistrybiological activitiestaxanes0104 chemical sciences010404 medicinal & biomolecular chemistrydiarylheptanoidsComplementary and alternative medicineMolecular Medicineanalytical toolsCorylus avellana
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Supramolecular Assembly of Metal Complexes by (Aryl)I⋯dz2[PtII] Halogen Bond

2020

The theoretical data for the half‐lantern complexes [Pt(C^N)(μ‐S^N)] 2 ( 1 – 3 ; С^N is cyclometalated 2‐Ph‐benzothiazole; S^N is 2‐SH‐pyridine 1 , 2‐SH‐benzoxazole 2 , 2‐SH‐tetrafluorobenzothiazole 3 ) indicate that the Pt···Pt orbital interaction leads to an increment of the nucleophilicity of the outer d z 2 ‐orbitals to provide assembly with electrophilic species. 1 – 3 were co‐crystallized with bifunctional halogen bond (XB) donors to give adducts ( 1 – 3 ) 2 ∙(1,4‐diiodotetrafluorobenzene) and infinite polymeric [ 1 ·1,1’‐diiodoperfluorodiphenyl] n . X‐ray crystallography revealed that the supramolecular assembly is achieved via (Aryl)I∙∙∙ d z 2 [Pt II ] XB between iodine σ‐holes and …

platinakemialliset sidoksetcyclometalated complexhalogen bondingsupramolekulaarinen kemiaplatinumkompleksiyhdisteetsupramolecular chemistrytheoretical calculations
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Inside Cover: Hydrogen-Bonded Open-Framework with Pyridyl-Decorated Channels: Straightforward Preparation and Insight into Its Affinity for Acidic Mo…

2017

International audience; A hydrogen-bonded open framework with pores decorated by pyridyl groups was constructed by off-charge-stoichiometry assembly of protonated tetrakis(4-pyridyloxymethyl)methane and [Al(oxalate)(3)](3-), which are the H-bond donor and acceptor of ionic H-bond interactions, respectively. This supramolecular porous architecture (SPA-2) has 1nm-large pores interconnected in 3D with large solvent-accessible void (53%). It demonstrated remarkable affinity for acidic organic molecules in solution, which was investigated by means of various carboxylic acids including larger drug molecules. Competing sorption between acetic acid and its halogenated homologues evidenced good sel…

porosityabsolute-structureHydrogenSupramolecular chemistrychemistry.chemical_element010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysissupramolecular chemistrycrystalhost-guest systemsPolymer chemistryMoleculesolid-state nmr[CHIM]Chemical Scienceshost frameworkssorption010405 organic chemistryHydrogen bondmicroporous materialsOrganic ChemistryarchitecturesSorptionGeneral Chemistrymetal-organic frameworkenantioselective separationOpen frameworkcations0104 chemical scienceschemistryadsorptionhydrogen bondsCover (algebra)
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Multifacial Recognition in Binary and Ternary Cocrystals from 5-Halouracil and Aminoazine Derivatives

2018

A systematic analysis using single crystal X-ray diffraction was performed to explore the role exerted by potential intercomponent proton-transfer reactions in the supramolecular structures of A–B cocrystals formed by 5-haloderivatives of uracil (A), coupled with 2-aminoadenine simulants (aminoazines, B). Twelve new heterodimers were synthesized in different stoichiometries and cocrystallized by solvent cogrinding followed by solution crystallization. In the binary cocrystals, uracil or 1-methyluracil with halide modification at the 5 position (F, Cl, Br, I) was coupled with amino-aromatic N-heterocycles (melamine, 2,4,6-triaminopyrimidine, 2,6-diaminopyridine) as a multivalent site for pyr…

proton transferPyrimidineX ray diffractionSupramolecular chemistry010402 general chemistry01 natural sciencesaromatic compounds; hydrogen bonds; ionization; proton transfer; X ray diffractionNucleobaselaw.inventionchemistry.chemical_compoundlawionizationsingle crystal X-raysGeneral Materials ScienceCrystallizationta116orgaaniset yhdisteet010405 organic chemistryHydrogen bondChemistryaromatic compoundsUracilGeneral ChemistrykiteetCondensed Matter Physics0104 chemical sciencesCrystallographyhalogen bondinghydrogen bondsTernary operationSingle crystalCrystal Growth & Design
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Halogen Bonds in 2,5-Dihalopyridine-Copper(I) Halide Coordination Polymers

2019

Two series of 2,5-dihalopyridine-Cu(I)A (A = I, Br) complexes based on 2-X-5-iodopyridine and 2-X-5-bromopyridine (X = F, Cl, Br and I) are characterized by using single-crystal X-ray diffraction analysis to examine the nature of C2&minus

pyridinedihalopyridineSupramolecular chemistrychemistry.chemical_elementHalidekupari010402 general chemistry01 natural scienceslcsh:TechnologyArticlechemistry.chemical_compoundkemialliset sidoksetPyridineGeneral Materials Sciencelcsh:Microscopypolymeeritlcsh:QC120-168.85chemistry.chemical_classificationHalogen bondlcsh:QH201-278.5010405 organic chemistrylcsh:TPolymerkompleksiyhdisteetCopper3. Good health0104 chemical sciencesCrystallographyhalopyridineschemistrylcsh:TA1-2040copperHalogenFluorinehalogeenisidoksetlcsh:Descriptive and experimental mechanicshalogen bondlcsh:Electrical engineering. Electronics. Nuclear engineeringlcsh:Engineering (General). Civil engineering (General)lcsh:TK1-9971
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Molecular Mechanisms of the Blockage of Glioblastoma Motility

2021

Glioblastoma (GBM) is the most common and lethal brain tumor. GBM has a remarkable degree of motility and is able to infiltrate the healthy brain. In order to perform a rationale-based drug-repositioning study, we have used known inhibitors of two small Rho GTPases, Rac1 and Cdc42, which are upregulated in GBM and are involved in the signaling processes underlying the orchestration of the cytoskeleton and cellular motility. The selected inhibitors (R-ketorolac and ML141 for Cdc42 and R-ketorolac and EHT 1864 for Rac1) have been successfully employed to reduce the infiltration propensity of GBM in live cell imaging studies. Complementarily, all-atom simulations have elucidated the molecular …

rac1 GTP-Binding Proteinrho GTP-Binding ProteinsGeneral Chemical EngineeringBrain tumorMotilityRAC1CDC42Library and Information SciencesBiologySettore BIO/09 - FisiologiaMicrotubules01 natural sciencesDownregulation and upregulationLive cell imaging0103 physical sciencesmedicineHumanscdc42 GTP-Binding Protein010304 chemical physicsDrug discoveryCancerGeneral Chemistrymedicine.disease0104 chemical sciencesComputer Science Applications010404 medicinal & biomolecular chemistrySettore CHIM/03 - Chimica Generale E InorganicaCancer researchGlioblastomaJournal of Chemical Information and Modeling
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CCDC 1524101: Experimental Crystal Structure Determination

2017

UCUZOK : 6,12,18,24-tetramethoxy-2,8,14,20-tetranonyl-4,10,16,22-tetrahydroxycalix[4]arene propan-2-ol solvate Space Group: P-1, Cell: a 12.27090(10)Å b 13.96500(10)Å c 19.53620(10)Å, α 83.2880(1)° β 89.0250(1)° γ 84.9650(1)° Work published 2017 via Cambridge Crystallographic Data Centre.

resorcinarenesolvatecalixarenemacrocyclesupramolecular chemistry
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CCDC 264161: Experimental Crystal Structure Determination

2017

WEJVOZ : New structure undergoing enhancement. Space Group: P21/c, Cell: a 18.5217(4)Å b 23.2973(6)Å c 21.1118(3)Å, α 90.00° β 96.591(1)° γ 90.00°. Work published 2017 via Cambridge Crystallographic Data Centre.

resorcinarenesolvateoctapodandcalixarenemacrocyclesupramolecular chemistry
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CCDC 750239: Experimental Crystal Structure Determination

2014

UDUXOI : 2,26,51,54-Tetraethyl-6,24,30,48-tetramethoxy-9,12,15,18,21,33,36,39,42,45-decaoxaheptacyclo[27.19.3.35,25.03,8.022,53.027,32.046,50]tetrapentaconta-1(48),3,5,7,22,24,27,29,31,46,49,52-dodecaene methanol solvate. Work published 2014 via Cambridge Crystallographic Data Centre.

resorcinarenesolvateresorcinarene-bis-crowncalixarenesupramolecular chemistry
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Phytochemical investigation of the needles of Abies nebrodensis (Lojac.) Mattei

2019

Abies nebrodensis (Lojac.) Mattei (Pinaceae) is a species living in a very small population only in a confined area of Sicily. In this study, the dichloromethane extract of the leaves was analyzed. Apart from three already known metabolites namely dehydroabietic acid; maltol; and rheosmin, previously detected in other species of Abies, a lanostane derivative was isolated. Its chemical structure was elucidated by means of extensive spectroscopic methods.

rheosminAbies nebrodensiChemical structurePopulationMaltolPlant Science01 natural sciencesBiochemistryLanostaneAnalytical ChemistrySettore BIO/01 - Botanica Generalechemistry.chemical_compoundOrganic chemistrySettore BIO/15 - Biologia FarmaceuticaAbies nebrodensiseducationeducation.field_of_studymaltolbiology010405 organic chemistrySettore BIO/02 - Botanica SistematicaOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryPhytochemicalPinaceaedehydroabietic acidlanostaneDerivative (chemistry)
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