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This reprint contains 11 papers published in a Special Issue of Molecules entitled "Crystal Structures of Metal Complexes". I will be very happy if readers will be interested in the crystal structures of metal complexes.
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This Special Issue of the International Journal of Molecular Science comprises a comprehensive study on “Metal Complex Interactions with Nucleic Acids and/or DNA”. This Special Issue has been inspired by the important contribution of Prof. Nick Hadjiliadis to the field of palladium or/and platinum/nucleic acid interactions. It covers a selection of recent research and review articles in the field of metal complex interactions with nucleic acids and/or DNA. Moreover, this Special Issue on "Metal Complexes Interactions with Nucleic Acids and/or DNA" provides an overview of this increasingly diverse field, presenting recent developments and the latest research with particular emphasis on metal-based drugs and metal ion toxicity.
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For the past 40 years, metal-based drugs have been widely used for the treatment of cancer. Cisplatin and follow-up drugs carboplatin (ParaplatinTM) and oxaliplatin (EloxatinTM) have been the gold standard for metallodrugs in clinical settings as antineoplastic agents. While effective, these drugs (either alone or in combination therapy) have faced a number of clinical challenges resulting from their limited spectrum of activity, high toxicity leading to significant side effects, resistance, poor water solubility, low bioavailability and short circulating time. In the past 10 years, various unconventional non-platinum metal-based agents have emerged as a potential alternative for cancer treatment. These compounds are highly effective and selective in cancers resistant to cisplatin and other chemotherapeutic agents. Research in this area has recently exploded with a relevant number of patents and clinical trials, in addition to reports in scientific journals. Furthermore, in parallel to the synthesis of coordination and organometallic compounds comprising many different metals and unconventional platinum-based derivatives, researchers are focused on optimizing mechanistic and pharmacological features of promising drug candidates. This Special Issue aims to highlight the latest advances in anticancer metallodrugs with a focus on unconventional anticancer agents, as well as novel activation, targeting and delivery strategies aimed at improving their pharmacological profile.
?–? stacking --- encapsulation --- n/a --- oxindolimine–metal complexes --- cyclodextrin --- platinum iodido complexes --- distribution coefficient --- antiproliferative activity --- anticancer agents --- nanotubes --- ruthenium --- platinum --- Log kw --- nanoparticles --- drug discovery --- metal complex --- metallodrugs --- isatin-derived ligands --- anticancer drug --- upconverting nanoparticles --- pyridine benzimidazole --- dendrimers --- liposomes --- thiophene --- angiogenesis --- micelles --- HSA oxidation --- platinum(IV) --- imaging --- chromatographic lipophilicity parameter --- amidophosphine --- copper and iron chelators in cancer --- Log P --- biomacromolecules --- bones --- DNA cleavage --- stopped-flow spectroscopy --- silver --- phosphonates --- transmetalation --- metallomics --- MRI --- fluorescence quenching --- partition coefficient --- gold fingers --- anticancer --- HSA binding --- gold --- ?0 --- targeting --- metastasis --- DNA interaction --- antimigration --- cytotoxicity --- HPLC --- ruthenium complexes --- zinc finger proteins --- Gold(III) complexes --- aquaporins --- antiproliferative --- protein-DNA recognition --- photoactivation --- lipophilicity --- cancer --- 1-methylcytosine --- PET --- ?-? stacking --- oxindolimine-metal complexes
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Homogeneous catalysis owes its success, in large part, to the development of a wide range of ligands with well-defined electronic and steric properties, which have thus made it possible to adjust the behavior of many organometallic complexes. However, ligands used in catalysis have long been centered on elements of group 15, and it is only more recently that carbon ligands have proved to be valuable alternatives with the emergence of cyclic diaminocarbenes (NHC).This Special Issue aims to provide a contemporary overview of the advances in carbon ligand chemistry from fundamental aspects to applications.
carbenes --- ylides --- DFT calculations --- electronic structure --- catalysis --- ligands --- structure–activity relationship --- NHC --- nanoparticle --- calixarene --- palladium catalyst --- Suzuki-Miyaura reaction --- amino-acids --- water --- carbon ligand --- amide --- negative charge --- phosphonium ylide --- oxide --- pincer --- metathesis --- ruthenium --- nitro catalysts --- NHC ligands --- olefins --- selenonium ylides --- selenonium salts --- chirality --- stereogenic selenium atom --- asymmetric synthesis --- optical resolution --- reactivity --- malaria --- Plasmodium falciparum --- gold --- NHC-ligands --- hybrid molecules --- drug resistance --- N-heterocyclic carbene --- platinum --- metal complexes --- 195Pt NMR --- N-heterocyclic carbenes --- imidazole --- spectroscopy --- X-ray --- mercury(II) complex --- T-shaped --- carbodiphosphorane --- phosphorus ylides --- pincer ligands --- coordination chemistry --- Cu(I) complex --- photoluminescence --- titanium --- hafnium --- copolymerization of epoxide with CO2 --- density functional theory --- natural bond orbitals --- aromaticity --- ion pairs --- alkali metals --- tropylidenyl ions --- cyclooctatetraene ions --- rhodium --- electron paramagnetic resonance (EPR) spectroscopy --- density functional theory (DFT) --- electrochemistry --- carbone complexes --- carbido complexes --- transition metal complexes --- chemical bonding --- pincer ligand --- macrocycle --- lithium --- potassium --- intramolecular C-H activation --- dehydrogenation --- carbone --- ligand --- germylene --- coordination --- ylide --- n/a --- structure-activity relationship
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In recent years, micro- and nanosystems with magnetic properties have been extensively investigated in many fields, ranging from physics to medicine. The research in these areas has lately shown that if the magnetic compounds are opportunely functionalized and modified with moieties and specific functional groups, a plethora of challenging multidisciplinary applications is available, including the development of magnetically controlled particles, stimuli-responsive materials, magnetically guided chemical/drug-delivery systems, sensors, spintronics, separation and purification of contaminated groundwater and soils, ferrofluids and magnetorheological fluids, contrast agents for MRI, and internal sources of heat for the thermoablation of cancer. Magnetic compounds have been found to be highly selective and effective in all these application fields, from the molecular level to the microscale. This book aims at underlining the latest advances in the field of magnetic compounds, nanosystems, and materials, covering a large variety of topics related to novel synthesis and functionalization methods and the properties, applications, and use of magnetic systems in chemistry, materials science, diagnostics, and medical therapy.
paramagnetic properties --- gadolinium oxide --- relaxation agents --- nanoparticles --- magnetic materials --- nanostructured materials --- magnetic nanoparticles --- magnetometry --- magnetic hysteresis --- magnetic domain visualization --- magnetic resonance imaging --- magnetic fluid hyperthermia --- magnetic particle toxicity --- magnetically-guided drug delivery systems --- magnetite nanoparticles --- magnetic resonance imaging (MRI), polymeric core–shells --- magnetic submicron core–shells --- drug delivery --- adsorption --- magnetic separation --- nanotechnology --- water treatments --- iron oxide nanoparticles --- positive contrast agents --- ligands --- molecular magnetism --- single-ion magnets (SIMs) or monometallic single-molecule magnets --- single-molecule magnets (SMMs) --- synthetic strategies --- 3d-, 4d- and 5d-metal complexes as SIMs and SMMs --- heavy metals --- nanocomposite --- hybrid --- multi-metal --- water --- magnetic particle and nanoparticles --- single-molecule magnets --- MRI contrast agents
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This book represents a collection of contributions in the field of the synthesis and characterization of chemical compounds, natural products, chemical reactivity, and computational chemistry. Among its contents, the reader will find high-quality, peer-reviewed research and review articles that were published in the open access journal Compounds by members of the Editorial Board and the authors invited by the Editorial Office and Editor-in-Chief.
Technology: general issues --- Chemical engineering --- atropisomerism --- 4,4′-bipyridine --- pyridine N-oxidation --- halogenation --- halogen bond --- cyanation --- Finkelstein reaction --- Suzuki coupling --- Orchis --- scent --- gas chromatography --- mass spectrometry --- solid-phase microextraction --- quantum chemistry --- computational chemistry --- molecular dynamics --- modeling --- open-source software --- proprietary software --- Himantoglossum --- solid phase microextraction --- iodination --- alkanes --- alkenes --- alkynes --- alkyl carbonyls --- elemental iodine --- iodides --- Zutano variety --- avocado oil --- Soxhlet extraction --- ultrasound-assisted extraction --- volatiles --- ripening --- over-ripe --- HS-SPME–GC–MS --- Basilicata --- Barlia robertiana --- Himantoglossum robertianum --- mantel test --- Orchidaceae --- pollination syndrome --- Italy --- volatile compounds --- solvolysis --- aryldiazonium ions --- perchlorate anions --- silicon carbide (SiC) --- 3C-SiC powder --- 4H-SiC crystal --- impurities --- photoluminescence --- pnictogen bonding --- nitrogen as pnictogen bond donor --- geometries --- crystal structure analysis --- ICSD and CSD database analyses --- MESP characterizations --- sum of the van der Waals radii concept --- Dactylorhiza --- volatile organic compounds --- thiosemicarbazone --- metal complexes --- DNA interactions --- biological activity --- thiazolidinedione --- microwave synthesis --- compound library --- rosiglitazone --- Knoevangel condensation --- biodiesel production --- crude glycerin --- carbon materials --- n/a --- 4,4'-bipyridine --- HS-SPME-GC-MS
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Plant-based diets contain a plethora of metabolites that may impact on health and disease prevention. Most are focused on the potential bioactivity and nutritional relevance of several classes of phytochemicals, such as polyphenols, flavonoids, carotenoids, phyto-oestrogens, and frucrooligo-saccharides. These compounds are found in fruit, vegetables, and herbs. Daily intakes of some of these compounds may exceed 100 mg. Moreover, intestinal bacterial activity may transform complex compounds such as anthocyanins, procyanidins, and isoflavones into simple phenolic metabolites. The colon is thus a rich source of potentially active phenolic acids that may impact both locally and systemically on gut health. Further, nondigestible fiber (prebiotics) are dietary substrates that selectively promote proliferation and/or activity of health-promoting bacterial populations in the colon. Prebiotics, such as inulin, raffinose, and stachyose, have a proven ability to promote the abundance of intestinal bacterial populations, which may provide additional health benefits to the host. Further, various pulse seed soluble (fiber) extracts are responsible for improving gastrointestinal motility, intestinal functionality and morphology, and mineral absorption. Studies indicated that the consumption of seed origin soluble extracts can upregulate the expression of BBM proteins that contribute for digestion and absorption of nutrients.
intra amniotic (in ovo) administration --- zinc gene expression --- iron gene expression --- brush border membrane functional genes --- intestinal bacterial populations --- villus surface area --- cichoric acid --- metal complexes --- cytotoxicity --- cancer --- bacterial strains --- fungi --- human cell culture --- lactic acid bacteria --- probiotic --- acrylamide --- viability --- flow cytometry --- mesotrione --- traumatic acid --- breast cancer --- herbicide --- antioxidant --- oxidative stress --- bifidobacteria --- colon --- fermentation --- microbiota --- prebiotic --- SHIME® --- artichoke --- intestinal microbiota --- vegetable drink --- beneficial microorganisms --- cereal --- legume --- pseudocereal --- fruit --- synbiotic --- microbiome --- SCFA --- pectin --- rhamnogalacturonan --- transepithelial electrical resistance (TEER) --- pea --- phytate --- iron --- bioavailability --- bio active compound --- in vivo --- Gallus gallus --- brush border membrane --- oats --- celiac disease --- non-celiac gluten sensitivity --- gluten-free --- SCFAs --- teff --- staple food crops --- prebiotics --- probiotics --- iron deficiency --- zinc deficiency --- gut microbiota --- intrauterine growth restriction (IUGR) --- fructose --- dexamethasone --- intestinal gluconeogenesis --- plant origin --- bio-active compounds --- intestine
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The amide bond represents a privileged motif in chemistry. The recent years have witnessed an explosion of interest in the development of new chemical transformations of amides. These developments cover an impressive range of catalytic N–C bond activation in electrophilic, Lewis acid, radical, and nucleophilic reaction pathways, among other transformations. Equally relevant are structural and theoretical studies that provide the basis for chemoselective manipulation of amidic resonance. This monograph on amide bonds offers a broad survey of recent advances in activation of amides and addresses various approaches in the field.
N-heterocyclic carbene --- non planar amide --- ruthenium (Ru) --- physical organic chemistry --- gemcitabine prodrug --- pyramidal amides --- bridged sultams --- catalysis --- dipeptides --- N-(1-naphthyl)acetamide --- C-N ? bond cleavage --- steric effects --- peptide bond cleavage --- transition-metal-free --- palladium --- N-heterocyclic carbenes (NHCs) --- addition reaction --- C–O activation --- rhodium --- metal complexes --- carbanions --- thioamidation --- amide bond --- intramolecular catalysis --- antiviral activity --- additivity principle --- pre-catalysts --- C–N bond cleavage --- bridged lactams --- C–H acidity --- arynes --- twisted amides --- organic synthesis --- amination --- Suzuki-Miyaura --- tert-butyl --- cyclopentadienyl complexes --- C-S formation --- enzymes --- DFT study --- sulfonamide bond --- N --- HERON reaction --- primaquine --- entropy --- amide activation --- amidation --- synthesis --- amide hydrolysis --- carbonylicity --- amide bond activation --- amide bond resonance --- aminosulfonylation --- molecular dynamics --- model compound --- in situ --- amide --- homogeneous catalysis --- heterocycles --- anomeric effect --- multi-component coupling reaction --- kinetic --- excited state --- C–H bond cleavage --- palladium catalysis --- amides --- thiourea --- formylation --- alkynes --- cis/trans isomerization --- amide C–N bond activation --- intein --- C-H functionalization --- succindiamide --- amide bonds --- crown ether --- aminoacylation --- directing groups --- cytostatic activity --- reaction thermodynamics --- acyl transfer --- transition metals --- N-dimethylformamide --- DMAc --- acylative cross-coupling --- C-H/C-N activation --- nickel catalysis --- antibacterial screening --- sodium --- aryl thioamides --- Winkler-Dunitz parameters --- catalyst --- N-dimethylacetamide --- base-catalyed hydrolysis --- nitrogen heterocycles --- cross-coupling --- insertion --- amidicity --- nitro-aci tautomerism --- activation --- carbonylation --- transamidation --- amine --- distortion --- Pd-catalysis --- rotational barrier energy --- hypersensitivity --- N–C activation --- metabolic stability --- [2+2+2] annulation --- twisted amide --- protease --- cyanation --- amide resonance --- trialkylborane --- catalysts --- biofilm eradication --- pharmacokinetics --- pancreatic cancer cells --- DMF --- aryl esters --- Michael acceptor --- fumardiamide --- water solvation --- ester bond activation --- cyclization --- nuclear magnetic resonance --- secondary amides --- reaction mechanism --- density functional theory --- density-functional theory --- amino acid transporters
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