Výsledky vyhľadávania - "Pyridines/chemistry"

Binding modes of a flexible ruthenium polypyridyl complex to DNA

Autori: Malagarriga, Meritxell González, Leticia

Zdroj: Phys Chem Chem Phys

Predmety: Pyrenes, Binding Sites, 103006 Chemical physics, Pyridines, Pyrenes/chemistry, DNA, Ruthenium/chemistry, Molecular Dynamics Simulation, Coordination Complexes/chemistry, 104017 Physikalische Chemie, Ruthenium, Intercalating Agents, Chemistry, Pyridines/chemistry, Coordination Complexes, 104017 Physical chemistry, 103006 Chemische Physik, Intercalating Agents/chemistry, DNA/chemistry

Popis súboru: application/pdf

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/39431730

A Self‐Assembled ATP Probe for Melanoma Cell Imaging

Autori: Zheng-wang Sun Hong Bo Cheng Nahyun Kwon a ďalší

Prispievatelia: Zheng-wang Sun Hong Bo Cheng Nahyun Kwon a ďalší

Zdroj: Chemistry – A European Journal. 25:3501-3504

Predmety: Models, Molecular, theranostics, Pyridines, Adenosine Triphosphate/analysis, 02 engineering and technology, 01 natural sciences, supramolecular chemistry, Cell Line, optical imaging, Adenosine Triphosphate, Melanoma/diagnostic imaging, Models, Pyridines/chemistry, Coordination Complexes, Cell Line, Tumor, melanoma, Humans, Fluorescent Dyes/chemistry, Melanoma, Fluorescent Dyes, Tumor, Optical Imaging, Molecular, Coordination Complexes/chemistry, Optical Imaging/methods, 0104 chemical sciences, ATP, 0210 nano-technology

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/30645046
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201806182
https://www.ncbi.nlm.nih.gov/pubmed/30645046
https://ir.ymlib.yonsei.ac.kr/handle/22282913/170430
https://ewha.elsevierpure.com/en/publications/a-self-assembled-atp-probe-for-melanoma-cell-imaging
https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201806182
https://dspace.ewha.ac.kr/handle/2015.oak/249542

Importance of Metal-Ion Exchange for the Biological Activity of Coordination Complexes of the Biomimetic Ligand N4Py

Autori: Arjan Geersing Nathalie Ségaud Monique G. P. van der Wijst a ďalší

Zdroj: Inorg Chem
Inorganic Chemistry

Predmety: Models, Molecular, Tumor, Intracellular Space/drug effects, Pyridines, Intracellular Space, Molecular Conformation, Molecular, Coordination Complexes/chemistry, Ligands, 01 natural sciences, Cell Line, 0104 chemical sciences, 3. Good health, Structure-Activity Relationship, Metals, Heavy/chemistry, Models, Pyridines/chemistry, Coordination Complexes, Cell Line, Tumor, Metals, Heavy, Humans

Prístupová URL adresa: https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.8b00714
https://pubmed.ncbi.nlm.nih.gov/29916702
https://hdl.handle.net/11370/78bda54e-daf6-48ab-a326-5de026326a7d
https://research.rug.nl/en/publications/78bda54e-daf6-48ab-a326-5de026326a7d
https://doi.org/10.1021/acs.inorgchem.8b00714
https://pubs.acs.org/doi/full/10.1021/acs.inorgchem.8b00714
http://europepmc.org/abstract/MED/29916702
https://dissem.in/p/103453534/importance-of-metal-ion-exchange-for-the-biological-activity-of-coordination-complexes-of-the-biomimetic-ligand-n4py/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030684
https://www.rug.nl/research/portal/files/62990400/acs.inorgchem.8b00714.pdf
https://pubmed.ncbi.nlm.nih.gov/29916702/

Structure–Function Evaluation of Imidazopyridine Derivatives Selective for δ-Subunit-Containing γ-Aminobutyric Acid Type A (GABAA) Receptors

Autori: Kirsten Yakoub Sascha Jung Christian Sattler a ďalší

Zdroj: Journal of Medicinal Chemistry. 61:1951-1968

Predmety: Pyridines, Imidazoles, GABA-A/metabolism, Receptors, GABA-A, 01 natural sciences, 0104 chemical sciences, 3. Good health, Inhibitory Concentration 50, Protein Subunits, Structure-Activity Relationship, Pyridines/chemistry, Imidazoles/chemistry, Receptors, Humans, Protein Subunits/metabolism, GABA-A Receptor Antagonists, GABA-A Receptor Antagonists/chemistry

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/29451785
https://pubsdc3.acs.org/doi/abs/10.1021/acs.jmedchem.7b01484
https://www.ncbi.nlm.nih.gov/pubmed/29451785
https://pubmed.ncbi.nlm.nih.gov/29451785/
https://pure.mpg.de/pubman/faces/ViewItemOverviewPage.jsp?itemId=item_2570424
https://pubs.acs.org/doi/10.1021/acs.jmedchem.7b01484
https://pubs.acs.org/doi/full/10.1021/acs.jmedchem.7b01484

Synthesis of novel 1H-Pyrazolo[3,4-b]pyridine derivatives as DYRK 1A/1B inhibitors

Prispievatelia: Areum Park Jieon Hwang Joo-Youn Lee a ďalší

Predmety: Antineoplastic Agents / chemical synthesis, Antineoplastic Agents / chemistry, Antineoplastic Agents / pharmacology, Cell Line, Tumor, Cell Proliferation / drug effects, Cell Survival / drug effects, Dose-Response Relationship, Drug, Drug Screening Assays, Antitumor, Humans, Molecular Structure, Protein Kinase Inhibitors / chemical synthesis, Protein Kinase Inhibitors / chemistry, Protein Kinase Inhibitors / pharmacology, Protein Serine-Threonine Kinases / antagonists & inhibitors, Protein Serine-Threonine Kinases / metabolism, Protein-Tyrosine Kinases / antagonists & inhibitors, Protein-Tyrosine Kinases / metabolism, Pyrazoles / chemical synthesis, Pyrazoles / chemistry, Pyrazoles / pharmacology, Pyridines / chemical synthesis, Pyridines / chemistry, Pyridines / pharmacology, Structure-Activity Relationship, Colon cancer, DYRK1A, DYRK1B

Relation: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS; J00326; https://ir.ymlib.yonsei.ac.kr/handle/22282913/187518; https://www.sciencedirect.com/science/article/pii/S0960894X21004534?via%3Dihub; T202124799

Dostupnosť: https://ir.ymlib.yonsei.ac.kr/handle/22282913/187518
https://doi.org/10.1016/j.bmcl.2021.128226
https://www.sciencedirect.com/science/article/pii/S0960894X21004534?via%3Dihub

Biological evaluation of dimethylpyridine–platinum complexes with potent antiproliferative activity

Autori: Robert Czarnomysy Agnieszka Gornowicz Anna Bielawska a ďalší

Zdroj: Journal of Enzyme Inhibition and Medicinal Chemistry. 31:150-165

Predmety: 0301 basic medicine, Dose-response relationship, Organoplatinum Compounds, Cell Survival, Pyridines, Pyridines - pharmacology, Antineoplastic agents - pharmacology, Antineoplastic Agents, Platinum - chemistry, Tumor cells, Organoplatinum compounds - chemical synthesis, Structure-Activity Relationship, 03 medical and health sciences, Tumor Cells, Cultured, Cell survival - drug effects, Humans, Antineoplastic agents - chemical synthesis, Flow cytometry, cultured, antitumor, Cell Proliferation, Platinum, Caspases - metabolism, Platinum - pharmacology, 0303 health sciences, Dose-Response Relationship, Drug, Molecular Structure, drug, Organoplatinum compounds - chemistry, Pyridines - chemistry, Structure-activity relationship, Flow Cytometry, Antineoplastic agents - chemistry, 3. Good health, Cell proliferation - drug effects, Drug screening assays, Caspases, Mitochondrial Membranes, Mitochondrial membranes - drug effects, Drug Screening Assays, Antitumor, Molecular structure

Prístupová URL adresa: https://www.tandfonline.com/doi/pdf/10.1080/14756366.2016.1212191?needAccess=true
https://pubmed.ncbi.nlm.nih.gov/27488500
https://www.tandfonline.com/doi/pdf/10.1080/14756366.2016.1212191
https://europepmc.org/article/MED/27488500
http://www.ncbi.nlm.nih.gov/pubmed/27488500
https://www.ncbi.nlm.nih.gov/pubmed/27488500
https://www.tandfonline.com/doi/full/10.1080/14756366.2016.1212191

Evaluating the In Vivo Specificity of [18F]UCB-H for the SV2A Protein, Compared with SV2B and SV2C in Rats Using microPET

Autori: Serrano, Maria Elisa Becker, Guillaume Bahri, Mohamed Ali a ďalší

Zdroj: Serrano , M E , Becker , G , Bahri , M A , Seret , A , Mestdagh , N , Mercier , J , Mievis , F , Giacomelli , F , Lemaire , C , Salmon , E , Luxen , A & Plenevaux , A 2019 , ' Evaluating the In Vivo Specificity of [18F]UCB-H for the SV2A Protein, Compared with SV2B and SV2C in Rats Using microPET ' , Molecules (Basel, Switzerland) , vol. 24 , no. 9 . https://doi.org/10.3390/molecules24091705

Predmety: Animals, Brain/diagnostic imaging, Levetiracetam/administration & dosage, Magnetic Resonance Imaging, Male, Membrane Glycoproteins/metabolism, Models, Animal, Molecular Structure, Nerve Tissue Proteins/metabolism, Positron-Emission Tomography, Pyridines/chemistry, Pyrrolidinones/chemistry, Rats, Sprague-Dawley, Sensitivity and Specificity

Dostupnosť: https://kclpure.kcl.ac.uk/portal/en/publications/0ef419a5-2b4d-407a-829b-7ff5e7e0a463
https://doi.org/10.3390/molecules24091705

Effects of novel alkyl pyridine platinum complexes on apoptosis in Ishikawa endometrial cancer cells

Zdroj: Medicinal Chemistry. 11(6):540-550

Predmety: Organoplatinum compounds - pharmacology, Dose-response relationship, Cells, Apoptosis - drug effects, drug, Antineoplastic agents - pharmacology, Organoplatinum compounds - chemistry, Platinum - chemistry, Fibroblasts - drug effects, Pyridines - chemistry, Structure-activity relationship, Organoplatinum compounds - chemical synthesis, Antineoplastic agents - chemistry, Cell proliferation - drug effects, Endometrial neoplasms - drug therapy, Drug screening assays, Cell survival - drug effects, Humans, Female, Antineoplastic agents - chemical synthesis, cultured, Molecular structure, antitumor, Endometrial neoplasms - pathology

Rho Kinase Inhibitors Prevent Endothelium-Dependent Contractions in the Rat Aorta

Autori: Mak, JC Man, RYK Chan, CKY a ďalší

Zdroj: The Journal of Pharmacology and Experimental Therapeutics. 329:820-826

Predmety: Male, 0301 basic medicine, Inbred SHR, rho-Associated Kinases - antagonists & inhibitors - biosynthesis, Pyridines, Vasoconstriction - drug effects, Blotting, Western, Aorta, Thoracic, Isometric Contraction - drug effects, Amides - chemistry - pharmacology, In Vitro Techniques, Rats, Inbred WKY, Vascular - drug effects - enzymology - physiology, Dose-Response Relationship, 03 medical and health sciences, Species Specificity, 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine, Isometric Contraction, Rats, Inbred SHR, Animals, Inbred WKY, Endothelium, Endothelium, Vascular - drug effects - enzymology - physiology, Aorta, Hypertension - drug therapy - enzymology - physiopathology, 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine - analogs & derivatives - chemistry - pharmacology, Antihypertensive Agents, rho-Associated Kinases, 0303 health sciences, Thoracic - drug effects - enzymology - physiopathology, Dose-Response Relationship, Drug, Blotting, Antihypertensive Agents - chemistry - pharmacology, Amides, Rats, 3. Good health, Pyridines - chemistry - pharmacology, Aorta, Thoracic - drug effects - enzymology - physiopathology, Vasoconstriction, Hypertension, Endothelium, Vascular, Drug, Western

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/19193928
https://www.ncbi.nlm.nih.gov/pubmed/19193928
https://core.ac.uk/display/37894916
https://jpet.aspetjournals.org/content/329/2/820
https://jpet.aspetjournals.org/content/329/2/820.full.pdf
http://hub.hku.hk/handle/10722/59230
http://jpet.aspetjournals.org/content/329/2/820.short
http://hdl.handle.net/10722/62839
http://hdl.handle.net/10722/59230
http://hdl.handle.net/10722/62819

Organogold(III) Supramolecular Polymers for Anticancer Treatment

Autori: Raymond Wai-Yin Sun Wei Lu Chi-Ming Che a ďalší

Zdroj: Angewandte Chemie. 124:4966-4970

Predmety: tumor, Porphyrins, Pyridines, Melanoma, Experimental, Antineoplastic Agents, Organogold compounds - chemistry - pharmacology, Supramolecular polymers, Antineoplastic agents - chemistry - pharmacology, 01 natural sciences, Spectrophotometry, ultraviolet, Porphyrins - chemistry - pharmacology, Mice, Cell Line, Tumor, ultraviolet, Animals, Humans, Melanoma, antitumor, Melanoma - drug therapy, Melanoma, experimental - drug therapy, Self-assembly, 3. Good health, Nanostructures, Drug screening assays, antitumor, 0104 chemical sciences, Pyridines - chemistry - pharmacology, Cell line, tumor, Spectrophotometry, Drug screening assays, Drug delivery, Spectrophotometry, Ultraviolet, Gold, experimental - drug therapy, Drug Screening Assays, Antitumor, Cell line, Organogold Compounds

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/22473661
https://www.ncbi.nlm.nih.gov/pubmed/22473661
https://europepmc.org/article/MED/22473661
https://www.infona.pl/resource/bwmeta1.element.wiley-ange-v-124-i-20-ange201108466
https://onlinelibrary.wiley.com/doi/full/10.1002/anie.201108466
https://core.ac.uk/display/37993061
http://hdl.handle.net/10722/168628

Comparative Study of the Affinity and Metabolism of Type I and Type II Binding Quinoline Carboxamide Analogues by Cytochrome P450 3A4

Autori: Dahal, Upendra P Joswig-Jones, Carolyn Jones, Jeffrey P

Zdroj: Journal of Medicinal Chemistry. 55:280-290

Predmety: Pyrazines - chemical synthesis, Pyrazines - chemistry, 0301 basic medicine, Pyridines - chemical synthesis, Pyrimidines - chemistry, Pyridines, Cytochrome P-450 CYP3A - chemistry, Hydroxylation, Substrate Specificity, Small Molecule Libraries, Quinolines - chemistry, Structure-Activity Relationship, 03 medical and health sciences, Catalytic Domain, Cytochrome P-450 CYP3A, 0303 health sciences, Pyridines - chemistry, Amides, Pyrimidines - chemical synthesis, Pyrimidines, Dealkylation, Pyrazines, Quinolines - chemical synthesis, Amides - chemistry, Quinolines, Cytochrome P-450 CYP3A Inhibitors, Amides - chemical synthesis, Protein Binding

Prístupová URL adresa: https://europepmc.org/articles/pmc3257383?pdf=render
https://pubmed.ncbi.nlm.nih.gov/22087535
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257383/
https://pubs.acs.org/doi/10.1021/jm201207h
http://europepmc.org/abstract/MED/22087535
https://www.ncbi.nlm.nih.gov/pubmed/22087535
https://pubs.acs.org/doi/pdf/10.1021/jm201207h

Synthesized pyridine compound derivatives decreased TNF alpha and adhesion molecules and ameliorated HSV-induced inflammation in a mouse model

Autori: Dongsik Bang Joohyon Kim Eun-So Lee a ďalší

Prispievatelia: Dongsik Bang Joohyon Kim Eun-So Lee a ďalší

Zdroj: European Journal of Pharmacology. 657:167-172

Predmety: Male, 0301 basic medicine, Pyridines, Down-Regulation/drug effects, Administration, Oral, Messenger/metabolism, Herpes simplex virus, Behcet Syndrome/genetics, Naphthyridines/chemistry, Tumor Necrosis Factor-alpha/metabolism, Mice, Simplexvirus, Pyridines/administration & dosage, Pyridines/pharmacology, Naphthyridines/administration & dosage, Naphthyridines/chemical synthesis, 0303 health sciences, Pyridine compound derivative, Behcet Syndrome, Behcet Syndrome/metabolism, 3. Good health, Administration, Cell Adhesion Molecules/genetics, Behcet Syndrome/virology, Oral, Naphthyridines/pharmacology, Cell Adhesion Molecules/metabolism, Simplexvirus/physiology, Tumor Necrosis Factor-alpha/biosynthesis, Down-Regulation, Mouse model, Cell Line, 03 medical and health sciences, Anti-inflammation, Behcet Syndrome/drug therapy, Animals, Humans, Pyridines/chemical synthesis, RNA, Messenger, Naphthyridines, Pyridines/chemistry, Animal, Tumor Necrosis Factor-alpha/antagonists & inhibitors, Tumor Necrosis Factor-alpha, Behcet's disease, Oral administration, Molecular Weight, Disease Models, Animal, Disease Models, RNA, Messenger/genetics, TNF alpha, Cell Adhesion Molecules

Popis súboru: 167~172

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/21315710
https://www.sciencedirect.com/science/article/pii/S0014299911001208
http://repository.ajou.ac.kr/handle/201003/6488
https://www.ncbi.nlm.nih.gov/pubmed/21315710
https://pubmed.ncbi.nlm.nih.gov/21315710/
http://www.sciencedirect.com/science/article/pii/S0014299911001208

Dicyano and Pyridine Derivatives of β-Carotene: Synthesis and Vibronic, Electronic, and Photophysical Properties

Autori: Cruz, Arvin John Filoteo Siam, Khamis Rillema, D. Paul a ďalší

Prispievatelia: Cruz, Arvin John Filoteo Siam, Khamis Rillema, D. Paul a ďalší

Zdroj: The Journal of Physical Chemistry A. 115:1108-1116

Predmety: Models, Molecular, Pyridines, beta Carotene/chemistry, 02 engineering and technology, Research Support, Crystallography, X-Ray, 01 natural sciences, Absorption, Electron Transport, Models, Pyridines/chemistry, Near-Infrared, 0204 chemical engineering, Non-U.S. Gov't, Spectroscopy, Carotenoids/chemistry, Non-P.H.S, Crystallography, Spectroscopy, Near-Infrared, Carotenoids/chemical synthesis, Molecular, beta Carotene, Carotenoids, 0104 chemical sciences, beta Carotene/analogs & derivatives, beta Carotene/chemical synthesis, Energy Transfer, X-Ray, Quantum Theory, U.S. Gov't, Electronics

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/21244068
https://europepmc.org/abstract/MED/21244068
http://pubs.acs.org/doi/abs/10.1021/jp103749b
https://pubmed.ncbi.nlm.nih.gov/21244068/
https://www.ncbi.nlm.nih.gov/pubmed/20518541
https://pubs.acs.org/doi/full/10.1021/jp106293s
https://core.ac.uk/display/59207838

The binding of β-d-glucopyranosyl-thiosemicarbazone derivatives to glycogen phosphorylase: A new class of inhibitors

Autori: Alexacou, Kyra-Melinda Tenchiu (Deleanu), Alia-Cristina Chrysina, Evangelia D. a ďalší

Prispievatelia: Alexacou, Kyra-Melinda Tenchiu (Deleanu), Alia-Cristina Chrysina, Evangelia D. a ďalší

Zdroj: Bioorganic & medicinal chemistry 18, 7911-7922 (2010). doi:10.1016/j.bmc.2010.09.039
Bioorganic & Medicinal Chemistry

Predmety: pyridine, Thiosemicarbazones, 0301 basic medicine, Glucopyranosyl-thiosemicarbazones, Enzyme Inhibitors: pharmacology, Glycogen Phosphorylase, Muscle Form: antagonists & inhibitors, Pyridines, Glucose: chemistry, Molecular Conformation, Organic chemistry, Chemistry, Medicinal, Crystallography, X-Ray, Thiosemicarbazones: chemical synthesis, 03 medical and health sciences, Pharmacy and materia medica, Halogens, Φαρμακευτική, Thiosemicarbazones: chemistry, Thiosemicarbazones: pharmacology, Catalytic Domain, Halogens: chemistry, Animals, Οργανική χημεία, Biology (General), Enzyme Inhibitors, Enzyme Inhibitors: chemical synthesis, Enzyme Inhibitors: chemistry, Inhibition, X-ray crystallography, glucose-1-phosphate, 0303 health sciences, Binding Sites, Glycogen phosphorylase, Glucosephosphates, Type 2 diabetes, 3. Good health, Glycogen Phosphorylase, Muscle Form: metabolism, Pyridines: chemistry, Kinetics, Χημεία (Γενικά), Glucose, Βιολογία (Γενικά), Chemistry (General), Glycogen Phosphorylase, Muscle Form, Glucosephosphates: chemistry, Rabbits, Protein Binding

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/20947361
http://www.rcsb.org/pdb/explore.do?structureId=3MSC
https://www.sciencedirect.com/science/article/pii/S096808961000876X
https://www.ncbi.nlm.nih.gov/pubmed/20947361
https://pubmed.ncbi.nlm.nih.gov/20947361/
https://www.rcsb.org/pdb/explore.do?structureId=3MSC
https://www.rcsb.org/structure/3MT9
https://bib-pubdb1.desy.de/record/96951

A Small Molecule That Blocks Fat Synthesis By Inhibiting the Activation of SREBP

Autori: Qian Mao Hea Young Park Choo Shinji Kamisuki a ďalší

Prispievatelia: Qian Mao Hea Young Park Choo Shinji Kamisuki a ďalší

Zdroj: Chemistry & Biology. 16:882-892

Predmety: Blood Glucose, 0301 basic medicine, Protein Structure, Sterol Regulatory Element Binding Proteins/chemistry, Transcription, Genetic, Pyridines, Sterol Regulatory Element Binding Proteins/metabolism, Clinical Biochemistry, Mice, Obese, CHO Cells, Biochemistry, Fatty Acids/biosynthesis, Obese, Mice, 03 medical and health sciences, Cricetulus, Genetic, Pyridines/chemistry, Thiazoles/chemistry, Sterol Regulatory Element Binding Proteins/antagonists & inhibitors, Cricetinae, Thiazoles/pharmacology, Drug Discovery, Animals, Humans, Molecular Biology, Pyridines/pharmacology, Pharmacology, Sterol Regulatory Element Binding Proteins, 2. Zero hunger, 0303 health sciences, Blood Glucose/metabolism, Body Weight, Fatty Acids, Intracellular Signaling Peptides and Proteins, Membrane Proteins, Protein Structure, Tertiary, 3. Good health, Fatty Acids/metabolism, Thiazoles, Intracellular Signaling Peptides and Proteins/metabolism, CHEMBIO, Molecular Medicine, Membrane Proteins/metabolism, CELLBIO, Transcription, Tertiary, Protein Binding

Popis súboru: application/pdf

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/19716478
https://tohoku.pure.elsevier.com/en/publications/a-small-molecule-that-blocks-fat-synthesis-by-inhibiting-the-acti
http://www.sciencedirect.com/science/article/pii/S1074552109002385
http://www.cell.com/cell-chemical-biology/abstract/S1074-5521(09)00238-5
https://repository.kulib.kyoto-u.ac.jp/dspace/handle/2433/112665
https://core.ac.uk/display/39243119
https://www.sciencedirect.com/science/article/pii/S1074552109002385

Structures and Solvatochromic Phosphorescence of Dicationic Terpyridyl–Platinum(II) Complexes with Foldable Oligo(ortho‐phenyleneethynylene) Bridging Ligands

Autori: Lu, W Zhu, MX Che, CM a ďalší

Zdroj: Chemistry – A European Journal. 14:9736-9746

Predmety: Models, Molecular, Luminescence, Magnetic Resonance Spectroscopy, Ethers - Chemistry, Organoplatinum Compounds, Photochemistry, Pyridines, Cations - Chemistry, Crystallography, X-Ray, Ligands, Electron, 01 natural sciences, Aggregation, Microscopy, Electron, Transmission, Models, Cations, Transmission, Hydrophobic effect, Pyridines - Chemistry, Alkynes - Chemistry, Platinum, Solvents - Chemistry, Microscopy, Crystallography, Luminescent Agents, Molecular Structure, Temperature, Molecular, Water, Phenyleneethynylene, 0104 chemical sciences, Organoplatinum Compounds - Chemistry, Spectrophotometry, Alkynes, Luminescent Measurements, X-Ray, Solvents, Luminescent Agents - Chemistry, Water - Chemistry, Ethers

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/18816539
https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/chem.200800394
http://onlinelibrary.wiley.com/doi/10.1002/chem.200800394/abstract
https://www.onlinelibrary.wiley.com/doi/abs/10.1002/chem.200800394
https://core.ac.uk/display/37992539
http://www.ncbi.nlm.nih.gov/pubmed/18816539
http://hub.hku.hk/handle/10722/168340
http://hdl.handle.net/10722/168340

Polyelectrolyte‐Induced Self‐Assembly of Positively Charged Alkynylplatinum(II)–Terpyridyl Complexes in Aqueous Media

Autori: Yam, VW Wong, KM Chan, KH a ďalší

Zdroj: Chemistry – A European Journal. 14:4577-4584

Predmety: Noncovalent interactions, Molecular Structure, Organoplatinum Compounds, Polymers, Pyridines, Osmolar Concentration, Water, Electrons, Self-assembly, Hydrogen-Ion Concentration, Pyridines - chemistry, Polyelectrolytes, 01 natural sciences, 0104 chemical sciences, Solutions, Electrolytes, Polymers - chemistry, Alkynes - chemistry, Alkynes, Organoplatinum Compounds - chemical synthesis - chemistry, Electrolytes - chemistry, UV/Vis spectroscopy, Platinum

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/18393348
https://www.onlinelibrary.wiley.com/doi/10.1002/chem.200800276
https://core.ac.uk/display/37902326
https://europepmc.org/article/MED/18393348
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.200800276
http://onlinelibrary.wiley.com/doi/10.1002/chem.200800276/full
https://www.ncbi.nlm.nih.gov/pubmed/18393348
http://hdl.handle.net/10722/68905

Luminescent Alkynylplatinum(II) Complexes of 2,6‐Bis(N‐alkylbenzimidazol‐2′‐yl)pyridine‐Type Ligands with Ready Tunability of the Nature of the Emissive States by Solvent and Electronic Property Modulation

Autori: Keith Man-Chung Wong Wai Han Lam Vivian Wing-Wah Yam a ďalší

Zdroj: Chemistry – A European Journal. 14:4562-4576

Predmety: Models, Molecular, Luminescence, Organoplatinum Compounds, Pyridines, Electrons, Crystallography, X-Ray, Ligands, 01 natural sciences, Computer chemistry, N ligands, Electrochemistry, Computer Simulation, Photoluminescence, Platinum, Molecular Structure, Spectrum Analysis, Stereoisomerism, Pyridines - chemistry, 0104 chemical sciences, Density functional calculations, Models, Chemical, Alkynes - chemistry, Alkynes, Luminescent Measurements, Organoplatinum Compounds - chemical synthesis - chemistry, Solvents, Spectrophotometry, Ultraviolet, Alkynyl ligands

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/18393346
https://core.ac.uk/display/37902998
https://europepmc.org/article/MED/18393346
https://onlinelibrary.wiley.com/doi/full/10.1002/chem.200701914
http://onlinelibrary.wiley.com/doi/10.1002/chem.200701914/abstract
https://www.ncbi.nlm.nih.gov/pubmed/18393346
http://hub.hku.hk/handle/10722/69835
http://hdl.handle.net/10722/69835

Pyridyne radical cations produced by photodissociation of Mg˙+(multifluoro-pyridine) complexes: A combined experimental and theoretical study

Autori: Liu, Hai-Chuan Zhang, Xin-Hao Wang, Changsheng a ďalší

Zdroj: Phys. Chem. Chem. Phys.. 9:607-615

Predmety: Time Factors, Free Radicals, Photochemistry, Pyridines, Ultraviolet Rays, Chemical, Magnesium: chemistry, 01 natural sciences, Models, Magnesium: radiation effects, Cations, Organometallic Compounds, Combinatorial Chemistry Techniques, Magnesium, Pyridines: radiation effects, Cations: radiation effects, Cations: chemistry, Organometallic Compounds: radiation effects, Molecular Structure, Organometallic Compounds: chemistry, Free Radicals: radiation effects, 0104 chemical sciences, Pyridines: chemistry, Models, Chemical, Quantum Theory, Free Radicals: chemistry

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/17242742
https://www.ncbi.nlm.nih.gov/pubmed/17242742
http://europepmc.org/abstract/MED/17242742
https://pubs.rsc.org/en/content/articlelanding/2007/cp/b614445d#!

Synthesis and biological activities of 7-aza rebeccamycin analogues bearing the sugar moiety on the nitrogen of the pyridine ring

Autori: Messaoudi, Samir Anizon, Fabrice Peixoto, P. a ďalší

Prispievatelia: Messaoudi, Samir Anizon, Fabrice Peixoto, P. a ďalší

Zdroj: Bioorganic & Medicinal Chemistry. 14:7551-7562

Predmety: Indoles, Nitrogen, Pyridines, 7-Azaindole, Physique, chimie, mathématiques & sciences de la terre, Carbazoles, Carbohydrates, Topoisomerase I inhibitors, 01 natural sciences, DNA binding agents, Cell Proliferation/drug effects, Mice, Structure-Activity Relationship, Carbazoles/chemical synthesis/chemistry/pharmacology, Physical, chemical, mathematical & earth Sciences, Pyridines/chemistry, Cell Line, Tumor, DNA/metabolism, Chimie, Animals, Humans, Indoles/chemical synthesis/chemistry/pharmacology, Enzyme Inhibitors/chemical synthesis/chemistry/pharmacology, Carbohydrates/chemistry, Enzyme Inhibitors, Antitumor compounds, Aza Compounds/chemical synthesis/chemistry/pharmacology, Nitrogen/chemistry, Cell Proliferation, Aza Compounds, Molecular Structure, DNA, [CHIM.ORGA] Chemical Sciences/Organic chemistry, DNA Topoisomerases, Type I/metabolism, Chk1 inhibitors, 3. Good health, 0104 chemical sciences, Chemistry, DNA Topoisomerases, Type I, Rebeccamycin, Checkpoint Kinase 1, Protein Kinases/metabolism, Topoisomerase I Inhibitors, Protein Kinases

Popis súboru: application/pdf

Prístupová URL adresa: https://hal.archives-ouvertes.fr/hal-00119572/file/BIOORG2006-2.pdf
https://pubmed.ncbi.nlm.nih.gov/16889964
https://orbi.uliege.be/handle/2268/86591
https://www.ncbi.nlm.nih.gov/pubmed/16889964
https://hal.archives-ouvertes.fr/hal-00119572/document
https://hal.archives-ouvertes.fr/hal-00119572
https://www.sciencedirect.com/science/article/abs/pii/S0968089606005682
https://hdl.handle.net/2268/86591
https://doi.org/10.1016/j.bmc.2006.07.013