Distribution of quinoline carboxylic acid derivatives in the dog prostate

The Prostate ◽  
1983 ◽  
Vol 4 (4) ◽  
pp. 407-414 ◽  
Author(s):  
Klaus M.-E. Jensen ◽  
Paul O. Madsen
Keyword(s):  
Carboxylic Acid ◽  
Quinoline Carboxylic Acid

scholarly journals Application of Pfitzinger Reaction in Synthesis of Hetero Ring Annelated Quinoline Carboxylic Acid Derivatives

2016 ◽  
Vol 28 (6) ◽  
pp. 1177-1180
Author(s):  
Taruna Yadav ◽  
Neelam K. Yadav ◽  
Manju Yadav ◽  
Bhawani Singh ◽  
D. Kishore
Keyword(s):  
Carboxylic Acid ◽  
Pfitzinger Reaction ◽  
Quinoline Carboxylic Acid

scholarly journals Exploration of Newer Possibilities to the Synthesis of Diazepine and Quinoline Carboxylic Acid Derivatives

2013 ◽  
Vol 2013 ◽  
pp. 1-8
Author(s):  
Vatsala Soni ◽  
Meenakshi Sharma ◽  
Anshu Agarwal ◽  
Dharma Kishore
Keyword(s):  
Carboxylic Acid ◽  
Drug Design ◽  
Spectral Data ◽  
Biological Activities ◽  
Design And Synthesis ◽  
Quinoline Carboxylic Acid ◽  
Quinoline Moiety ◽  
Molecular Framework

Heterocyclic systems containing benzothiazoles, carbazole (and azacarbazole) moieties have attracted the attention of chemists owing to these nuclei having been identified in the literature as most promising pharmacophores in drug design and synthesis. Based on these observations, it could be anticipated that incorporation of the bioactive azepine moiety and quinoline moiety into the molecular framework of benzothiazoles fused to carbazole (and azacarbazoles) could produce interesting series of compounds9–12with enhanced biological activities, whose structure was unequivocally established from its microanalyses and spectral data.

scholarly journals SAR-Based Optimization of a 4-Quinoline Carboxylic Acid Analogue with Potent Antiviral Activity

2013 ◽  
Vol 4 (6) ◽  
pp. 517-521 ◽  
Author(s):  
Priyabrata Das ◽  
Xiaoyi Deng ◽  
Liang Zhang ◽  
Michael G. Roth ◽  
Beatriz M. A. Fontoura ◽  
...  
Keyword(s):  
Carboxylic Acid ◽  
Antiviral Activity ◽  
Potent Antiviral Activity ◽  
Acid Analogue ◽  
Quinoline Carboxylic Acid

scholarly journals Influence of Ni (II) oxime complex coupled with the combination of diverse sized ZnO nanoparticles on Photovoltaic Performance

2020 ◽  
Vol 3 (2) ◽  
pp. 41-57
Author(s):  
Prashanth Kumar P.N. ◽  
Sajan Ponnappa ◽  
Ravi Hethegowdanahally Rajegowda ◽  
Amol Naik ◽  
Maxwell Selase Akple
Keyword(s):  
Solar Cell ◽  
Carboxylic Acid ◽  
Zno Nanoparticles ◽  
Photovoltaic Performance ◽  
Dye Sensitized Solar Cell ◽  
Zno Films ◽  
Dye Sensitized ◽  
Photovoltaic Efficiency ◽  
Quinoline Carboxylic Acid ◽  
Zno Particles

The one side selective synthesis of quinoline carboxylic acid oxime complex was carried out successfully. The as-prepared quinoline carboxylic acid oxime complex was complexed with nickel (II) salts to form nickel (II) oxime complex. These complexes were further adsorbed onto ZnO  films containing ZnO nanoparticles of various sizes. ZnO films containing a diverse proportion of ZnO nanoparticles were investigated to enhance the photovoltaic efficiency of the dye-sensitized solar cell. The as-synthesized complex was characterized by scanning electron microscopy (SEM), Ultra violet visible spectroscopy (UV-vis), Fourier Transform Infrared Spectroscopy (FT-IR) spectroscopy, 1Hydrogen Nuclear magnetic resonance spectroscopy (1HNMR), Liquid chromatography coupled with mass spectrometry (LC-MR), Brunauer–Emmett–Teller (BET), and Attenuated total reflection Infra-red spectroscopy (ATR-IR). The combination of large and small ZnO nanoparticles has significantly improves the photovoltaic efficiency. The optimum mixing ratio for the best performance (0.127%) of a dye-sensitized solar cell is achieved by mixing the small: large ZnO particles in a ratio 60:40. The increased efficiency is due to the harvesting of light caused by scattering effect from larger sized ZnO particles. The ZnO layer consisting of smaller particles which are very next to the ZnO bigger particles makes a good electronic contact between film electrode and the Indium-doped tin oxide glass substrate resulting in the increases in the dye molecules adsorption. The over-layered, large-sized ZnO particles enhance the light-harvesting by light scattering effect. Compared to the other mixtures of ZnO films, there is a decrease in the photovoltaic performance of the solar cell when ZnO particles (small and large in a ratio 1:1) were adsorbed onto the Ni (II) oxime complex, which are caused due to the decrease in the surface area and dye aggregation.

Absorption, Translocation, and Metabolism of AC 252 214 in Soybean (Glycine max), Common Cocklebur (Xanthium strumarium), and Velvetleaf (Abutilon theophrasti)

Weed Science ◽  
1985 ◽  
Vol 33 (4) ◽  
pp. 469-471 ◽  
Author(s):  
Dale L. Shaner ◽  
Patricia A. Robson
Keyword(s):  
Glycine Max ◽  
Carboxylic Acid ◽  
Half Life ◽  
Abutilon Theophrasti ◽  
Xanthium Strumarium ◽  
Quinoline Carboxylic Acid

The herbicide AC 252 214 {2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl] 3-quinoline-carboxylic acid} was absorbed by the roots and foliage of soybean [Glycine max (L.) Merr. ‘Williams’], common cocklebur (Xanthium strumarium L. ♯ XANST), and velvetleaf (Abutilon theophrasti Medic. ♯ ABUTH), and then translocated in the xylem and phloem to meristematic regions. AC 252 214 was metabolized rapidly by soybean and velvetleaf but appeared to be metabolized slowly by cocklebur. The order of tolerance of these three species to AC 252 214 was soybeans > velvetleaf > cocklebur. This order of tolerance was directly correlated in young plants with the half-life of AC 252 214 within the tissue. Velvetleaf exhibited increased tolerance to AC 252 214 with age, which was attributed partially to greatly reduced absorption of the herbicide by older leaves and more rapid metabolism of the herbicide.

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