Results 61 to 70 of about 38,082 (231)

Pursing Quinoline-8-Sulfonamide derivatives for the identification of potent NPPs inhibitors: In silico molecular docking, molecular dynamics simulations and density field theory (DFT) studies

open access: yesResults in Chemistry
Nucleotide pyrophosphatase/phosphodiesterase (NPP) enzymes belong to a broad category of ectonucleotidase enzymes. These NPPs are responsible for hydrolysis of extracellular nucleotides (ATP to AMP) and are therefore important regulators in the ...
Jamshed Iqbal   +10 more
doaj   +1 more source

Aza‐Büchner–Curtius–Schlotterbeck Reaction Enables Selective Construction of Quaternary Carbon Centers

open access: yesAngewandte Chemie International Edition, EarlyView.
We introduce the Aza‐Büchner–Curtius–Schlotterbeck (ABCS) reaction: A mild, catalyst‐free method for homologating aryl imines. Diverging from the traditional BCS mechanism, the diazo intermediate undergoes selective C─C insertion to form an all‐carbon quaternary center.
Simon O. Angerer   +6 more
wiley   +1 more source

Crystal structure of ethyl 2-(3,5-difluorophenyl)quinoline-4-carboxylate

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
In the title compound, C18H13F2NO2, the two rings of the quinoline system are fused almost coaxially, with a dihedral angle between their planes of 2.28 (8)°. The plane of the attached benzene ring is inclined to the plane of the quinoline system by 7.65 
V. M. Sunitha   +5 more
doaj   +1 more source

From classical to contemporary: A review on the synthesis and biological activities of quinoline and its derivatives [PDF]

open access: yesScripta Medica
Quinoline-derived analogues have considerable significant attention due to their wide range of pharmacological activities and promising therapeutic applications.
Kaur Harmanbir   +3 more
doaj   +1 more source

Crystalline Quinolinate Phosphoribosyltransferase

open access: yesJournal of Biological Chemistry, 1965
Abstract Quinolinate phosphoribosyltransferase catalyzes the formation of nicotinic acid mononucleotide, carbon dioxide, and inorganic pyrophosphate from quinolinic acid and 5-phosphoribosyl 1-pyrophosphate. The enzyme has a molecular weight of 165,000 and can be irreversibly dissociated into inactive protein units with a molecular weight of 54,000 ...
P M, Packman, W B, Jakoby
openaire   +2 more sources

Design, Synthesis, and Characterization of Tautomeric Quinoline-4-Carboxylic Acid–Based Esters, Amides, and Fused Heterocycles

open access: yesJournal of Chemistry
Quinoline-4-carboxylic acid derivatives are widely studied owing to their structural versatility and relevance in pharmaceutical sciences. In this study, 3-benzoyl-2-oxo-1,2-dihydroquinoline-4-carboxylic acid was synthesized via a solvent-free reaction ...
Derviş Gök
doaj   +1 more source

Structural modifications of quinoline-based antimalarial agents: Recent developments

open access: yesJournal of Pharmacy and Bioallied Sciences, 2010
Antimalarial drugs constitute a major part of antiprotozoal drugs and have been in practice for a long time. Antimalarial agents generally belong to the class of quinoline which acts by interfering with heme metabolism. The recent increase in development
Sandhya Bawa   +3 more
doaj   +1 more source

Crystal structure of bis(2,2′-bipyridine)[N′-(quinolin-2-ylmethylidene)pyridine-2-carbohydrazide]ruthenium(II) bis(tetrafluoridoborate) dichloromethane trisolvate

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
The title compound, [Ru(C10H8N2)2(C16H12N4O)](BF4)2·3CH2Cl2, crystallizes with one complex dication, two BF4− counter-anions and three dichloromethane solvent molecules in the asymmetric unit.
Asami Mori   +2 more
doaj   +1 more source

Benzimidazole-Quinoline Hybrids: Synthesis and Antimicrobial Properties

open access: yesPharmaceuticals
Background: Heterocyclic compounds are particularly important in medicinal chemistry. With a range of therapeutic uses, benzimidazoles and quinolines are both key heterocycles in medicinal chemistry.
Maria Marinescu
doaj   +1 more source

An ETH‐LAD trip with unfavourable consequences: A case report

open access: yesBritish Journal of Clinical Pharmacology, EarlyView.
Numerous analogues of the psychedelic and internationally controlled hallucinogen LSD have been described; however, only a limited number have been systematically investigated. This report presents the first case with an analytically confirmed ingestion of ETH‐LAD (6‐ethyl‐6‐nor‐lysergic acid diethylamide), the N‐ethyl derivative of LSD.
Johannes Nadler   +6 more
wiley   +1 more source

Home - About - Disclaimer - Privacy