Results 1 to 10 of about 82,349 (282)

N-(Quinolin-8-yl)quinoline-2-carboxamide [PDF]

Acta Crystallographica Section E, 2012
In the title compound, C19H13N3O, the dihedral angle between the two quinoline systems is 11.54 (3)°. The molecular conformation is stabilized by intramolecular N—H...N and C—H...O hydrogen bonds, with N—H.
Yanfeng Li, Hongbo Zhou, Xiaoping Shen
doaj   +3 more sources

Benzimidazole-Quinoline Hybrids: Synthesis and Antimicrobial Properties [PDF]

Pharmaceuticals
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   +2 more sources

A Review on Synthesis of Quinoline Analogs as Antimalarial, Antibacterial and Anticancer agents

Ethiopian Journal of Science and Sustainable Development, 2021
Numerous natural products possessing quinoline moiety exhibit interesting biological and pharmacological properties, such as antimalarial, antibacterial, antiasthmatic, antihypertensive, anti-inflammatory, immunosuppressive, antileishmanial, and ...
Ayana Melaku Yadessa, Digafie Zeleke
doaj   +1 more source

Biodegradation of Quinoline by a Newly Isolated Salt-Tolerating Bacterium Rhodococcus gordoniae Strain JH145

Microorganisms, 2022
Quinoline is a typical nitrogen-heterocyclic compound with high toxicity and carcinogenicity which exists ubiquitously in industrial wastewater. In this study, a new quinoline-degrading bacterial strain Rhodococcus sp.
Yinhu Jiang, Fuyin Zhang, Siqiong Xu, Pan Yang, Xiao Wang, Xuan Zhang, Qing Hong, Jiguo Qiu, Cuiwei Chu, Jian He   +9 more
doaj   +1 more source

Application of Quinoline Ring in Structural Modification of Natural Products

Molecules, 2023
Natural compounds are rich in pharmacological properties that are a hot topic in pharmaceutical research. The quinoline ring plays important roles in many biological processes in heterocycles.
Yu-Qing Zhao, Xiaoting Li, Hong-Yan Guo, Qing-Kun Shen, Zhe-Shan Quan, Tian Luan   +5 more
doaj   +1 more source

Cross-Feeding between Members of Thauera spp. and Rhodococcus spp. Drives Quinoline-Denitrifying Degradation in a Hypoxic Bioreactor

mSphere, 2020
The complex bacterial community in a quinoline-degrading denitrifying bioreactor is predominated by several taxa, such as Thauera and Rhodococcus.
Xinxin Wu, Xiaogang Wu, Ji Li, Qiaoyu Wu, Yiming Ma, Weikang Sui, Liping Zhao, Xiaojun Zhang   +7 more
doaj   +1 more source

The Trypanosoma cruzi enzyme TcGPXI is a glycosomal peroxidase and can be linked to trypanothione reduction by glutathione or tryparedoxin. [PDF]

, 2002
Trypanosoma cruzi glutathione-dependent peroxidase I (TcGPXI) can reduce fatty acid, phospholipid, and short chain organic hydroperoxides utilizing a novel redox cycle in which enzyme activity is linked to the reduction of trypanothione, a parasite ...
Docampo, Flohe, Moreno, Viode, Henderson, Walsh, Krauth-Seigel, Muller, Nogoceke, Tetaud, Wilkinson, Wilkinson, Tetaud, Wilkinson, Boveris, Fairlamb, Mehlotra, Carnieri, Kendall, Kelly, Gibson, Martinez-Calvillo, Kelly, Kelly, Kelly, Cannata, Rutter, Easterby, Gommel, Steinert, Sommer, Opperdoes, Opperdoes, Michels, Parsons, Blattner, Bjornstedt, Sztajer, Horiguchi, Holgren, Fabianek, Shih, Shih, van den Bosch, Subramani, Keller, Singh, Singh, Boveris, Duffieux, Goodman, Knoops, Yamashita, Verdoucq, Seo, Lopez, Krieger   +56 more
core   +4 more sources

Effect of Quinoline on the Phospholipid Profile of Curvularia lunata and Its Microbial Detoxification

Molecules, 2022
Quinoline is an N-heterocyclic compound commonly found in wastewater, especially that derived from coal processing, chemical, and pharmaceutical industries. In the present study, the microscopic fungus Curvularia lunata IM 4417, which is known to degrade
Aleksandra Felczak, Katarzyna Zawadzka, Przemysław Bernat, Marta Nowak-Lange, Katarzyna Lisowska   +4 more
doaj   +1 more source

Scientific Opinion on the re-evaluation of Quinoline Yellow (E 104) as a food additive:Question No EFSA-Q-2008-223 [PDF]

, 2009
The Panel on Food Additives and Nutrient Sources added to Food provides a scientific opinion re-evaluating the safety of Quinoline Yellow (E 104). Quinoline Yellow has been previously evaluated by the Joint FAO/WHO Expert Committee on Food Additives ...
Bal-Price, Bateman, BIBRA (The British Industrial Biological Research Association), Blevins, EC (European Commission), EFSA (European Food Safety Authority), EFSA (European Food Safety Authority), Fuglsang, Fuglsang, Fujita, Hannuksela, Hansen, Hollstein, JECFA (Joint FAO/WHO Expert Committee on Food Additives), JECFA (Joint FAO/WHO Expert Committee on Food Additives), JECFA (Joint FAO/WHO Expert Committee on Food Additives), JECFA (Joint FAO/WHO Expert Committee on Food Additives), JECFA (Joint FAO/WHO Expert Committee on Food Additives), Juhlin, Larsen, Lau, LEMM, Lu, Lück, Macioscek, McCann, NIOSH (National Institute for Occupational Safety and Health), Oettel, Ostergaard, Prival, Radio, SCF (Scentific Committee on Food), Scotter, Simon, Supramaniam, TemaNord, Viola, Worm, Young   +38 more
core   +2 more sources

Perfluoro effect in the photoelectron spectra of quinoline and isoquinoline [PDF]

, 1972
The high-resolution He 584Aophotoelectron spectra of heptafluoroquinoline and heptafluoroisoquinoline are compared with those of the parent compounds. Shifts in π ionisation potentials, due to the fluorine substitution, can be described with an inductive
Ham, D.M.W. van den, Meer, D. van der
core   +3 more sources