scholarly journals Synthesis, cytotoxic evaluation and DNA binding study of 9-fluoro-6H-indolo[2,3-b]quinoxaline derivatives

RSC Advances ◽  
2017 ◽  
Vol 7 (66) ◽  
pp. 41869-41879 ◽  
Author(s):  
Zhenyu Gu ◽  
Yanci Li ◽  
Songliang Ma ◽  
Shenghui Li ◽  
Guoqiang Zhou ◽  
...  
Keyword(s):  
Dna Binding ◽  
Antitumor Activity ◽  
Quaternary Ammonium ◽  
Quaternary Ammonium Salts ◽  
Binding Study ◽  
Ammonium Salts ◽  
Binding Ability ◽  
Quinoxaline Derivatives

New quaternary ammonium salts of 9-fluoro-6H-indolo[2,3-b] derivatives were synthesized. These compounds possessed enhanced DNA binding ability and improved antitumor activity.

Structure and Binding Properties of Four New Oligomeric Cyclophane Esters: 1,4-Xylylene 1,4-Phenylene Diacetates and Dipropionates

1998 ◽  
Vol 51 (5) ◽  
pp. 361 ◽  
Author(s):  
Donato Donati ◽  
Stefano Roelens ◽  
Riccardo Torriti ◽  
Giovanni Valle
Keyword(s):  
Crystal Structure ◽  
Quaternary Ammonium ◽  
Quaternary Ammonium Salts ◽  
Ammonium Salts ◽  
Binding Properties ◽  
Binding Ability ◽  
X Ray ◽  
Structure Determinations

The X-ray crystal structure determinations of four new oligomeric cyclophane esters are reported. They are: (3a) monomeric 1,4-xylylene (1,4-phenylene)diacetate, P21/n (No. 14), a 5·959(5), b 15·795(5), c 8·094(5) Å, β 108·060(5)°, V 724·3(8) Å3 , Z 2, R1(2σ) 0·0522, wR2 0·125; (3b) monomeric 1,4-xylylene (1,4-phenylene)dipropionate, P21/c (No. 14), a 5·878(1), b 14·642(2), c 18·909(2) Å, β 96·00(10)°, V 1618·5(4) Å3 , Z 4, R1(2σ) 0·053, wR2 0·165; (3c) dimeric 1,4-xylylene (1,4-phenylene)diacetate, P-1 (No. 2), a 14·633(2), b 17·529(2), c 5·736(1) Å, α 98·30(10), β 90·60(10), γ 95·40(10)°, V 1449·0(4) Å3, Z 2, R1(2σ) 0·057, wR2 0·158; (3d) dimeric 1,4-xylylene (1,4-phenylene)dipropionate, P21/a (No. 14), a 8·145(1), b 11·379(2), c 17·401(2) Å, β 101·40(10)°, V 1580·9(4) Å3, Z 4, R1(2σ) 0·034, wR2 0·095. Monomeric cyclophanes (3a,b) exhibit a well defined cleft, while dimeric (3c,d) adopt a flat conformation devoid of cavities. Binding properties were determined by 1H n.m.r. titrations in CDCl3 at T = 296 K. Complexation experiments with quaternary ammonium salts revealed that host (3c) possesses appreciable binding ability toward N-methylpyridinium (–ΔG° = 5·9 kJ mol-1), tetramethylammonium (–ΔG° = 8·8 kJ mol-1) and acetylcholine (–ΔG° = 7·5 kJ mol-1) cations, despite its lack of a preorganized cavity.

Synthesis and stability of 1-aminoalkylphosphonic acid quaternary ammonium salts

2021 ◽  
Author(s):  
Tomasz K. Olszewski ◽  
Anna Brol
Keyword(s):  
Phosphonic Acid ◽  
Quaternary Ammonium ◽  
Alkylating Agent ◽  
Quaternary Ammonium Salts ◽  
Ammonium Salts ◽  
Aminoalkylphosphonic Acid

An effective protocol for quaternization of simple 1-aminoalkylphosphonic acids under basic conditions and using Me2SO4 as convenient alkylating agent is reported. In the course of reaction phosphonic acid quaternary ammonium...

scholarly journals Green Accelerated Synthesis, Antimicrobial Activity and Seed Germination Test of Quaternary Ammonium Salts of 1,2-bis(4-pyridyl)ethane

Molecules ◽  
2019 ◽  
Vol 24 (13) ◽  
pp. 2424 ◽  
Author(s):  
Tăbăcaru ◽  
Botezatu ◽  
Horincar ◽  
Furdui ◽  
Dinică
Keyword(s):  
Escherichia Coli ◽  
Triticum Aestivum ◽  
Seed Germination ◽  
Quaternary Ammonium ◽  
Pathogenic Bacteria ◽  
Classical Method ◽  
Triticum Aestivum L ◽  
Quaternary Ammonium Salts ◽  
Ammonium Salts ◽  
Radicle Growth

A family of fifteen quaternary ammonium salts (QAs), bearing the 1,2-bis(4-pyridyl)ethane core, were obtained using for the first time two different green methods, such as microwave (MW) and ultrasounds (US) irradiation, with very good yields and in much shorter times compared to the classical method, and an assay on their antimicrobial action against Escherichia coli (E. coli) was carried out. While 12 to 24 hours were required for complete alkylation of 1,2-bis(4-pyridyl)ethane by reactive halogenated derivatives in anhydrous solvent under reflux conditions, MW and US irradiation reduced the reaction time and the desired products were achieved in a few min. One of the aims of this study was to evaluate the antibacterial potential of the synthesized QAs against pathogenic bacteria, along with their impact on germination activity of wheat seeds (Triticum aestivum L.). The antibacterial activity of the QAs against Escherichia coli was explored by determining the minimum inhibitory concentration (MIC). The MIC values varied from 0.312 to 2.5 mg/mL, highlighting the lowest values attained for the derivatives containing methoxy, chlorine and benzofurane functional groups. The viability of aerobic bacteria was determined with the Tetrazolium/Formazan Test, a method that was found to be the best alternative approach with respect to the difuzimetric method. Seeds of Triticum aestivum L. were used for the evaluation of the germination indicators, such as seed germination (SG), the relative seed germination (RSG), the relative radicle growth (RRG), and the seed germination index (GI). The toxicity studies of QAs 1, 4 and 7, at two different concentrations, showed no inhibitory effect on seed germination.

Interaction of water-insoluble quaternary ammonium salts with the hydrated silica surface

1996 ◽  
Vol 32 (6) ◽  
pp. 331-334
Author(s):  
V. V. Turov ◽  
O. A. Zaporozhets ◽  
O. Yu. Nadzhafova ◽  
V. V. Sukhan
Keyword(s):  
Quaternary Ammonium ◽  
Silica Surface ◽  
Quaternary Ammonium Salts ◽  
Ammonium Salts ◽  
Hydrated Silica

Curare-like Action of Polymethylene bis-Quaternary Ammonium Salts

Nature ◽  
1948 ◽  
Vol 161 (4097) ◽  
pp. 718-718 ◽  
Author(s):  
R. B. BARLOW ◽  
H. R. ING
Keyword(s):  
Quaternary Ammonium ◽  
Quaternary Ammonium Salts ◽  
Ammonium Salts
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