Results 21 to 30 of about 14,380 (267)

Induction of Cell Death in Human A549 Cells Using 3-(Quinoxaline-3-yl) Prop-2-ynyl Methanosulphonate and 3-(Quinoxaline-3-yl) Prop-2-yn-1-ol

open access: yesMolecules, 2019
Despite major advancements in the development of various chemotherapeutic agents, treatment for lung cancer remains costly, ineffective, toxic to normal non-cancerous cells, and still hampered by a high level of remissions.
Mixo Aunny Sibiya   +5 more
doaj   +1 more source

Sinteza i biološko djelovanje novih 1-benzil i 1-benzoil 3-heterocikličkih derivata indola [PDF]

open access: yes, 2010
Starting from 1-benzyl- (2a) and 1-benzoyl-3-bromoacetyl indoles (2b) new heterocyclic, 2-thioxoimidazolidine (4a,b), imidazolidine-2,4-dione (5a,b), pyrano(2,3-d)imidazole (8a,b and 9a,b), 2-substituted quinoxaline (11a,b–17a,b) and triazolo(4,3-a ...
A. Barry   +23 more
core   +2 more sources

Functionalization of diazines and benzo derivatives through deprotonated intermediates. [PDF]

open access: yes, 2008
International audienceThis critical review targets as a readership researchers generally oriented toward organic synthesis and in particular those active in heterocyclic chemistry.
Chevallier, Floris, Mongin, Florence
core   +2 more sources

2-(4-Chloroanilino)quinoxaline [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2008
There are two mol-ecules in the asymmetric unit of the title compound, C(14)H(10)ClN(3), with dihedral angles of 5.11 (10) and 13.61 (10)° between the aromatic ring systems. In the crystal structure, mol-ecules are linked by N-H⋯N hydrogen bonds, resulting in chains propagating in [010].
Idris, A.   +4 more
openaire   +5 more sources

Silica Bonded S-Sulfonic Acid: A Recyclable Catalyst for the Synthesis of Quinoxalines at Room Temperature

open access: yesMolecules, 2009
The reaction of 3-mercaptopropylsilica (MPS) and chlorosulfonic acid in chloroform afforded silica bonded S-sulfonic acid (SBSSA), which was used as a catalyst for the room temperature synthesis of quinoxaline derivatives from 1,2-diamino compounds and 1,
Khodabakhsh Niknam   +2 more
doaj   +1 more source

Dual Allosteric Effect in Glycine/NMDA Receptor Antagonism: A Comparative QSAR Approach

open access: yesPharmaceuticals, 2010
A comparative Hantzsch type QSAR study was conducted using multiple regression analysis on various sets of quinoxalines, quinoxalin-4-ones, quinazoline-2-carboxylates, 4-hydroxyquinolin-2(1H)-ones, 2-carboxytetrahydroquinolines, phenyl-hydroxy-quinolones,
Vipin B. Gupta, Manish Sharma
doaj   +1 more source

Biotransformation of quinoxaline by Streptomyces badius [PDF]

open access: yesLetters in Applied Microbiology, 1996
Quinoxaline, a mutagenic azaarene produced in foods during cooking, was added to cultures of Streptomyces badius ATCC 39117. After 24 h, the cultures were extracted with ethyl acetate. Two major metabolites were purified by liquid chromatography and identified by mass spectrometry and nuclear magnetic resonance spectroscopy as 3,4-dihydro-2(1H ...
Sutherland, J. B.   +3 more
openaire   +3 more sources

Fused-Ring Derivatives of Quinoxalines: Spectroscopic Characterization and Photoinduced Processes Investigated by EPR Spin Trapping Technique

open access: yesMolecules, 2014
10-Ethyl-7-oxo-7,10-dihydropyrido[2,3-f]quinoxaline derivatives, synthesized as promising biologically/photobiologically active compounds were characterized by UV/vis, FT-IR and fluorescent spectroscopy.
Zuzana Barbieriková   +5 more
doaj   +1 more source

Synthesis and Antimicrobial Activity of Some New Substituted Quinoxalines

open access: yesMolecules, 2019
A number of new symmetrically and asymmetrically 2,3-disubstituted quinoxalines were synthesized through functionalization of 2,3-dichloroquinoxaline (2,3-DCQ) with a variety of sulfur and/or nitrogen nucleophiles.
Mohamed A. El-Atawy   +3 more
doaj   +1 more source

SYNTHESIS OF QUINOXALINES

open access: yes, 2023
Quinoxalines are a group of antibiotics widely used in medicine to fight bacterial infections.These antibiotics have a broad spectrum of action and belong to the class of 4 quinolones. Theirmechanism of action is based on inhibiting the activity of bacterial enzymes responsible for DNAsynthesis, which leads to their death. Due to this, quinoxalines are
openaire   +1 more source

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