Relevant bibliographies by topics / N-Phenylanthranilic Acid

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'N-Phenylanthranilic Acid'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "N-Phenylanthranilic Acid"

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Martín, Ana, Rolando F. Pellón, Miriam Mesa, Maite L. Docampo, and Victoria Gómez. "Microwave-assisted Synthesis of N-phenylanthranilic Acids in Water." Journal of Chemical Research 2005, no. 9 (2005): 561–63. http://dx.doi.org/10.3184/030823405774308998.

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N-Phenylanthranilic acid derivatives were synthesised using the Ullmann condensation of 2-chlorobenzoic acid with aniline derivatives under microwave irradiation in aqueous media. The method offers better yields in shorter reaction times compared to classical heating approaches using water as solvent.
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2

Bala, Madhu, Rachna Yadav, and Amit Girdhar. "Synthesis and Characterization of Ester Derivatives of N-Phenylanthranilic Acid." Asian Journal of Chemistry 36, no. 10 (2024): 2269–74. http://dx.doi.org/10.14233/ajchem.2024.32215.

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N-Phenylanthranilic acid (fenamic acid) serves as the fundamental structure for synthesizing several non-steroidal anti-inflammatory drugs, antibacterial drugs and also functions as a modulator of membrane transport. To reduce the dose-related side effects of existing drugs, research is focussing to improve fenamic acid derivative solubility and bioavailability. A series of ester derivatives of N-phenylanthranilic acid (MB-1 to MB-5) viz. 2-(phenyl amino)methyl benzoate, 2-(phenyl amino)ethyl benzoate, 2-(phenyl amino)isopropyl benzoate,2-(phenyl amino)butyl benzoate and 2-(phenyl amino)phenyl
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3

Gaidukevich, A. N., E. Ya Levitin, A. A. Kravchenko, et al. "Synthesis and biological activity of N-phenylanthranilic acid derivatives." Pharmaceutical Chemistry Journal 19, no. 3 (1985): 180–82. http://dx.doi.org/10.1007/bf00770449.

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Ozkan, S. Zh, I. S. Eremeev, G. P. Karpacheva, and G. N. Bondarenko. "Oxidative Polymerization of N-Phenylanthranilic Acid in the Heterophase System." Open Journal of Polymer Chemistry 03, no. 03 (2013): 63–69. http://dx.doi.org/10.4236/ojpchem.2013.33012.

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Almasirad, Ali, Rohollah Hosseini, Hassan Jalalizadeh, et al. "Synthesis and Analgesic Activity of 2-Phenoxybenzoic Acid and N-Phenylanthranilic Acid Hydrazides." Biological & Pharmaceutical Bulletin 29, no. 6 (2006): 1180–85. http://dx.doi.org/10.1248/bpb.29.1180.

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Svechnikova, O. M., S. V. Kolisnyk, O. F. Vinnyk, T. A. Kostina, and T. V. Zhukova. "The molecular design of biologically active derivatives of N-phenylanthranilic acid." Journal of Organic and Pharmaceutical Chemistry 16, no. 1(61) (2018): 49–53. http://dx.doi.org/10.24959/ophcj.18.937.

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7

Wang, Yi-Xiang J., Graham Betton, Eike Floettmann, and Carsten Liess. "MRI histopathology correlation of N-phenylanthranilic acid induced nephropathy in rats." British Journal of Radiology 79, no. 948 (2006): 1009–10. http://dx.doi.org/10.1259/bjr/47913384.

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Hamiaux, Cyril, Lesley Larsen, Hui Wen Lee, et al. "Chemical synthesis and characterization of a new quinazolinedione competitive antagonist for strigolactone receptors with an unexpected binding mode." Biochemical Journal 476, no. 12 (2019): 1843–56. http://dx.doi.org/10.1042/bcj20190288.

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Abstract Strigolactones (SLs) are multifunctional plant hormones regulating essential physiological processes affecting growth and development. In vascular plants, SLs are recognized by α/β hydrolase-fold proteins from the D14/DAD2 (Dwarf14/Decreased Apical Dominance 2) family in the initial step of the signaling pathway. We have previously discovered that N-phenylanthranilic acid derivatives (e.g. tolfenamic acid) are potent antagonists of SL receptors, prompting us to design quinazolinone and quinazolinedione derivatives (QADs and QADDs, respectively) as second-generation antagonists. Initia
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Ozkan, Sveta Zhiraslanovna, Lyudmila Ivanovna Tkachenko, Oleg Nikolaevich Efimov, et al. "Advanced Electrode Coatings Based on Poly-N-Phenylanthranilic Acid Composites with Reduced Graphene Oxide for Supercapacitors." Polymers 15, no. 8 (2023): 1896. http://dx.doi.org/10.3390/polym15081896.

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The electrochemical behavior of new electrode materials based on poly-N-phenylanthranilic acid (P-N-PAA) composites with reduced graphene oxide (RGO) was studied for the first time. Two methods of obtaining RGO/P-N-PAA composites were suggested. Hybrid materials were synthesized via in situ oxidative polymerization of N-phenylanthranilic acid (N-PAA) in the presence of graphene oxide (GO) (RGO/P-N-PAA-1), as well as from a P-N-PAA solution in DMF containing GO (RGO/P-N-PAA-2). GO post-reduction in the RGO/P-N-PAA composites was carried out under IR heating. Hybrid electrodes are electroactive
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Endo, Satoshi, Toshiyuki Matsunaga, Midori Soda, et al. "Selective Inhibition of the Tumor Marker AKR1B10 by Antiinflammatory N-Phenylanthranilic Acids and Glycyrrhetic Acid." Biological & Pharmaceutical Bulletin 33, no. 5 (2010): 886–90. http://dx.doi.org/10.1248/bpb.33.886.

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Dissertations / Theses on the topic "N-Phenylanthranilic Acid"

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Fu, Kai-Ling, and 傅凱伶. "The Study of Microwave Accelerated Organic Reaction(1) Synthesis of N-Phenylanthranilic Acids(2) Synthesis of N-Substituted Pyrrole-2-carboxaldehyde." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/45843931195172457629.

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碩士<br>中興大學<br>化學系所<br>94<br>We report herein our studies on microwave-assisted N-phenylanthranilic acids formation and the synthesis of N-substituted pyrrole-2-carboxaldehyde. I. Preparation of N-phenylanthranilic acids The reaction times of the formation of N-phenylanthranilic acids, by reacting o-chlorobenzoic acid and substituted aniline, were greatly reduced from 2~4 hours in conventional method to 10 min by using domestic microwave irradiation at 800 W, and focused microwave irradiation at 270 W, while the yields were comparable. The above reaction did not work under neat or solid sup
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Book chapters on the topic "N-Phenylanthranilic Acid"

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"A Research Note on Synthesis in the Interfacial Conditions of Hybrid Dispersed Magnetic Nanomaterial Based on Poly-n-Phenylanthranilic Acid and Fe3O4." In Chemistry and Chemical Biology. Apple Academic Press, 2014. http://dx.doi.org/10.1201/b17413-15.

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Journal articles
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