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Quinoline derivatives
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Breast cancer is the most common malignancy globally, and is considered a major cause of cancer-related death. Tremendous effort is exerted to identify an optimal anticancer drug with limited side effects. The quinoline derivative RIMHS-Qi-23 had a wide-spectrum antiproliferative activity against various types of cancer cells.
12p
vialfrednobel
23-12-2023
3
3
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In this study, the thermodynamic dissociation constants of two new quinoline derivatives including (6-hydroxyl-3-sulfoquinoline-7-yloxy) acetic acid and (5-bromo-6-hydroxyl-N-methyl-3-sulfoquinoline-7-yloxy) acetic acid were initially determined in an aqueous solution using potentiometric titration at (25.0 ± 0.1) oC in the ionic medium of 0.10 M KCl solution.
9p
visharma
20-10-2023
5
2
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In this paper, we report the synthesis of five new 4-aza-2,3-didehydropodophyllotoxins by a straightforward multicomponent reaction in the hope of finding new structures with interesting anticancer activity. The novelty in our work is the preparation of quinoline structural compounds of podophyllotoxin derivatives, in two simple steps, having functional groups which are available for further modifications.
8p
vidudley
20-02-2023
5
2
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A short and easy route is described for 6,8-disubstituted derivatives of quinoline and 1,2,3,4-tetrahydroquinoline from 6,8-dibromoquinolines 2 and 7 by various substitution reactions. While copper-promoted substitution of 6,8- dibromide 2 produced monomethoxides 3 and 4, a prolonged reaction time mainly afforded dimethoxide 6 instead of 5, whose aromatization with DDQ and substitution reaction of dibromide 7 with NaOMe in the presence of CuI also gave rise to dimethoxide 6.
13p
langthannam
29-12-2021
5
0
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The synthesis, characterization, and spectroscopic properties of novel nonperipherally tetrasubstituted metallophthalocyanines (zinc, cobalt, copper, manganese, and indium) bearing 4 (7-(trifluoromethyl)quinolin-4-yl)oxy units has been reported. The new compounds have been characterized using UV-Vis, IR, 1H NMR, 13C NMR, 19F NMR, and mass spectroscopic data. The absorption properties of these new complexes were compared to those of peripherally substituted phthalocyanine derivatives.
11p
langthannam
29-12-2021
12
0
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The new compounds 7a–k, 8a–k, and 9a–k were synthesized from flavonones 4–6, which can be considered new precursors for quinoline synthesis through a one-step reaction. All the target compounds (7a–k, 8a–k, and 9a–k) were evaluated for their in vitro antimicrobial activity against nine test microorganisms. They showed the most activity against Mycobacterium smegmatis with minimum inhibitory concentrations (MIC) of 62.5–500 µg/mL, indicating their potential uses as antituberculosis agents. Among them 8a–k (m-fluoride) were the most active compounds against M. smegmatis (MIC, 62.5–125 µg/mL).
17p
langthannam
29-12-2021
11
0
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Pd/C-PPh3–CuI catalyzed Sonogashira cross-coupling of the 2-aryl-6,8-dibromo-2,3-dihydroquinolin-4(1H)-ones with phenyl acetylene or 3-butyn-1-ol afforded the corresponding 8-alkynylated quinolin-4(1H)-one derivatives, exclusively. Double carbo-substitution to afford the 6,8-dialkynyl derivatives was observed when PdCl2(PPh3)2 was used as Pd(0) source.
16p
langthannam
29-12-2021
2
0
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A simple and efficient one-pot synthesis of novel thieno[3’,2’:5,6]pyrimido[1,2-a]quinoline-2-carboxylates (5a– d) and their spirooxindole derivatives (12a–d) was accomplished. Thus, the Michael addition reaction of the cyclic β-enaminone 3 with the corresponding α, β-unsaturated nitrile derivatives 4a–d in refluxing EtOH in the presence of piperidine afforded 5a–d in good yields. On the other hand, spirooxindole derivatives 12a–d were synthesized by the reaction of cyclic β-enaminone 3 with the corresponding 3-cyanomethylidene-2-oxoindoles 11a–d in refluxing EtOH.
7p
langthannam
29-12-2021
16
0
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One-pot synthesis of novel quinoline- and quinolone-substituted 1,2,3-triazoles has been performed from the key intermediates, quinoline- and quinolone-substituted propargyl derivatives 1–3 (48%–88% yields). The antioxidant properties of the newly synthesized compounds, 1a–1c, 2a–2c, and 3a–3c, were evaluated by monitoring DPPH (2,2- diphenyl-1-picrylhydrazyl) radical scavenging abilities, metal chelating effects, and reducing power. The scavenging effects of compounds on the free radical decreased in the order of 3b > 3a > 1b and were found to be 36.3%, 34.9%, and 27.
14p
tudichquannguyet
29-11-2021
13
0
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In the present study, the antioxidant properties of peripherally and nonperipherally water-soluble tetra (quinoline 5-sulfonic acid) substituted metal-free (1, 2), Zn(II) (3, 4), Co(II) (5, 6), and Mn(III)Cl (7, 8) phthalocyanine (Pc) derivatives were reported. In order to determine the antioxidant properties of the Pc compounds, three different commonly known antioxidant methods were used: DPPH (α,α-diphenyl-β-picrylhydrazyl) radical scavenging, ferrous ion chelating, and reducing power assays.
10p
tudichquannguyet
29-11-2021
10
0
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The (E)-2-(2-hydroxystyryl)quinolin-8-ol (abbreviated as HSQ) molecule was synthesized and characterized. The ESIPT, solvatochromism properties, electronic structure, and ground and excited electric dipole moments of this molecule were measured using absorption and fluorescence spectra recorded in 13 different solvents. Its electronic structure via electronic transitions was investigated to find the quantitative values of solvatochromism properties by LSER calculations. The ESIPT mechanism was clarified; ground and excited dipole moments were determined using solvatochromic shift methods.
19p
tudichquannguyet
29-11-2021
6
1
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Polyethylene glycol (PEG) is a polymer that is widely used as a carrier for drug delivery systems (DDS). A library of N-PEGylated quinoline derivatives of PEG molecular weight 200 was prepared rapidly after the activation of PEGs using maleic anhydride. Quinoline with a polymer backbone is essential as new material. PEG is a water-soluble nonionic polymer approved by food and drug organizations for medicine applications. Because of its nontoxic grapheme, it is widely utilized in numerous biochemical, cosmetic, pharmaceutical, and industrialized applications.
20p
tudichquannguyet
29-11-2021
12
1
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Quinoline moiety is an important scaffold in the field of drug discovery and drug development, with a wide range of pharmacological activities. Quinoline derivatives are potent inhibitors for reverse transcriptase, which is responsible for the conversion of single-stranded viral RNA into double-stranded viral DNA.In the present study, we have designed and synthesized 2 series, namely pyrazoline and pyrimidine containing quinoline derivatives as non nucleoside reverse transcriptase inhibitors (NNRTIs).
46p
tudichquannguyet
29-11-2021
5
1
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Nitrogen containing heterocyclic compounds has acquired their remarkable and distinct place in the wide area of organic synthesis due to the broad range of applications. Among them, quinoline motifs have attracted researchers in the synthetic chemistry because of its presence in the large number of pharmacologically active compounds. Different methods for synthesis of quinoline derivatives are reported, among them the Friedlander synthesis have provided comparatively more efficient approach.
28p
tudichquannguyet
29-11-2021
15
1
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The purpose of the thesis research: Synthesis of new complexes of platinum and rare-earth elements containing quinoline's derivatives that are resistant to cancer cells, high antimicrobial activity or good fluorescence.
27p
tunelove
10-06-2021
15
4
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2,9-Bis[2-(pyrrolidin-1-yl)ethoxy]-6-{4-[2-(pyrrolidin-1-yl)ethoxy] phenyl}-11H-indeno[1,2-c]quinolin-11- one (BPIQ) is a derivative from 6-arylindeno[1,2-c]quinoline. Our previous study showed the anti-cancer potential of BPIQ compared to its two analogues topotecan and irinotecan.
10p
vimoscow2711
29-08-2020
9
1
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Methicillin Resistant Staphylococcus aureus (MRSA) consists of strains of S. aureus which are resistant to methicillin. The resistance is due to the acquisition of mecA gene which encodes PBP2a unlike of any PBPs normally produced by S. aureus.
14p
vijiraiya2711
27-05-2020
6
0
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Quinoline derivatives have diverse biological activities including anticancer activity. On the other hand, many sulfonamide derivatives exhibited good cytotoxic activity. Hybrids of both moieties may present novel anticancer agents.
13p
vijiraiya2711
27-05-2020
16
0
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Some compounds of substituted tetrazolo[1,5-a]quinolines were synthesized by reacting these 2-chloro derivatives with sodium azide in DMF as solvent. The structures of obtained compounds have been confirmed using spectroscopic methods (IR, NMR and MS).
7p
cathydoll4
21-02-2019
33
0
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The following silver and copper complexes in which quinine is coordinated via the two possible donor atoms was prepared and characterized. Coordination of quinine via the hydroxyl oxygen and quinoline nitrogen is observed in C20H25N2O2Cu2(SO4)2.6H2O and C20H25N2O2Ag2(SO4). The existence of the proton at the coordinated hydroxyl oxygen is also observed in these complexes. The coordination mode and the conformation of quinine can be derived from IR and Raman spectra and by using NMR techniques.
5p
uocvong04
24-09-2015
36
3
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