Relevant bibliographies by topics / Primary Moiety for The Synthesis of Several Antimicrobial

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Academic literature on the topic 'Primary Moiety for The Synthesis of Several Antimicrobial'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Primary Moiety for The Synthesis of Several Antimicrobial"

1

Journal, Baghdad Science. "Synthesis and Evaluation of Antimicrobial activity of several new Maleimides to Benzothiazole moiety." Baghdad Science Journal 10, no. 3 (2013): 658–72. http://dx.doi.org/10.21123/bsj.10.3.658-672.

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In this work, a series of new maleimides linked to substituted benzothiazole moiety were synthesized. Synthesis of these new cyclic imides were performed via three steps, the first one involved preparation of a series of 2-aminobenzothiazole substituted with different substituents via reaction of different primary aromatic amines with ammonium thiocyanate and bromine in glacial acetic acid. The prepared 2- amino benzothiozoles were introduced in the second step in reaction with maleic anhydride producing a series of N-(substituted benzothiazole-2-yl) maleamic acids.The resulted maleamic acids
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2

Azzawi, Ahlam Marouf AL, and Suroor Abdul Rhahman Mahdi. "Synthesis and Evaluation of Antimicrobial activity of several new Maleimides to Benzothiazole moiety." Baghdad Science Journal 10, no. 3 (2013): 658–72. http://dx.doi.org/10.21123/bsj.2013.10.3.658-672.

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In this work, a series of new maleimides linked to substituted benzothiazole moiety were synthesized. Synthesis of these new cyclic imides were performed via three steps, the first one involved preparation of a series of 2-aminobenzothiazole substituted with different substituents via reaction of different primary aromatic amines with ammonium thiocyanate and bromine in glacial acetic acid. The prepared 2- amino benzothiozoles were introduced in the second step in reaction with maleic anhydride producing a series of N-(substituted benzothiazole-2-yl) maleamic acids.The resulted maleamic acids
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3

Taj, Muhammad Babar, Muneera D. F. Alkahtani, Uzma Ali, et al. "New Heteroleptic 3D Metal Complexes: Synthesis, Antimicrobial and Solubilization Parameters." Molecules 25, no. 18 (2020): 4252. http://dx.doi.org/10.3390/molecules25184252.

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The microbial resistance to current antibiotics is increasing day by day, which in turn accelerating the development of new effective drugs. Several studies have proved the high antimicrobial potential of the interaction of several organic ligands with a variety of metal ions. In the present study, a conventional method has been adopted in the synthesis of twelve new heteroleptic complexes of cobalt (II), nickel (II), copper (II) and zinc (II) using three aldimines, namely, (HL1 ((E)-2-((4-chloro-2-hydroxybenzylidene)amino)-3,4-dimethyl-5-phenylcyclopent-2-en-1-one), HL2 ((Z)-3-((4-chlorobenzy
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4

Desiatkina, Oksana, Serena K. Johns, Nicoleta Anghel, et al. "Synthesis and Antiparasitic Activity of New Conjugates—Organic Drugs Tethered to Trithiolato-Bridged Dinuclear Ruthenium(II)–Arene Complexes." Inorganics 9, no. 8 (2021): 59. http://dx.doi.org/10.3390/inorganics9080059.

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Tethering known drugs to a metalorganic moiety is an efficient approach for modulating the anticancer, antibacterial, and antiparasitic activity of organometallic complexes. This study focused on the synthesis and evaluation of new dinuclear ruthenium(II)–arene compounds linked to several antimicrobial compounds such as dapsone, sulfamethoxazole, sulfadiazine, sulfadoxine, triclosan, metronidazole, ciprofloxacin, as well as menadione (a 1,4-naphtoquinone derivative). In a primary screen, 30 compounds (17 hybrid molecules, diruthenium intermediates, and antimicrobials) were assessed for in vitr
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5

Eikemo, Vebjørn, Leiv K. Sydnes, and Magne O. Sydnes. "Photodegradable antimicrobial agents − synthesis, photodegradation, and biological evaluation." RSC Advances 11, no. 51 (2021): 32339–45. http://dx.doi.org/10.1039/d1ra06324c.

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6

Lupascu, Dan, Lenuta Profire, Maria Apotrosoaei, et al. "Synthesis and Antimicrobial Activities of Novel Rutin Derivatives Carrying Quinoline Moiety." Revista de Chimie 71, no. 6 (2020): 401–7. http://dx.doi.org/10.37358/rc.20.6.8206.

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Antimicrobial resistance constitutes a topical subject and it is one of the major threats to public health. According to statistics, the incidence of multidrug-resistant microorganisms, such as bacteria, fungi and protozoa has increased in the last decades and it continues to spread. Therefore, the development of novel antimicrobial agents to combat drug-resistant infections is very important, among other research directions in this field. Quinoline ring is a very interesting structure for researchers because of its diverse biological properties (antimicrobial, anticancer, anticonvulsant, anti
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7

Pathak, Ashutosh, P. Malairajan Arti Gautam, and Shibu Das. "Isatin: A Short Review of their Antimicrobial Activities." International Journal of Current Microbiology and Applied Sciences 11, no. 1 (2022): 61–77. http://dx.doi.org/10.20546/ijcmas.2022.1101.009.

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Isatin(2, 3-dioxindate), a particularly effective scaffold with a variety of pharmacological actions, has been developed due to its therapeutic significance in organic and medicinal chemistry. Many researchers have been drawn to this skeleton because of its diverse biological response profile and its multiple possibilities against a variety of activities. Sandmeyer's and Stolle processes are two typical ways for synthesizing isatin derivatives. Many researchers have taken advantage of the isatin moiety by using NH at the first position, C2 and C3 carbonyl positions for the creation of numerous
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8

López-López, Lluvia Itzel, Denisse de Loera, Ernesto Rivera-Avalos, and Aidé Sáenz-Galindo. "Green Synthesis of Hydantoins and Derivatives." Mini-Reviews in Organic Chemistry 17, no. 2 (2020): 176–84. http://dx.doi.org/10.2174/1570193x16666181206100225.

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The hydantoin moiety is found in several bioactive compounds with important pharmacological properties such as antimicrobial, antifungal, anti-androgens, anticancer and the historical action anticonvulsant. Because of these reasons, the synthesis of these compounds and their derivatives is important to review considering the philosophy of the green chemistry. In this review, we present the actual importance in the green synthesis of hydantoins and their derivatives using green methods, such as microwave and ultrasound irradiation, ionic liquids, solid-phase and solvent-free synthesis. Finally,
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9

Sultan, Mohammed Ibrahim, Ahmed M. Abdula, Rana I. Faeq, and Mahdi F. Radi. "New Pyrazoline Derivatives Containing Imine Moiety: Synthesis, Characterization and Antimicrobial Study." Al-Mustansiriyah Journal of Science 32, no. 3 (2021): 8. http://dx.doi.org/10.23851/mjs.v32i3.955.

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A new series of pyrazoline derivatives (3-10) have been synthesized and characterized on the basis of FT-IR, 1H-NMR, and Mass techniques. 1-(4-Aminophenyl)-3-(pyridin-4-yl)prop-2-en-1-one (1) as a starting material was prepared by the reaction of 4-aminoacetophenone and 4-pyridinecarboxaldehyde in ethanol, using sodium hydroxide as a catalyst. Pyrazoline derivatives 2 was obtained via the cyclization reaction of compound 1 by the action of hydrazine hydrate 80% in ethanol. The target derivatives (3-8) were obtained by the reaction of pyrazoline derivative (2) with the corresponding aldehyde in
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10

V., N. PATOLIA, K. PATEL P., and J. BAXI A. "Studies on 4-Thiazolidinones. Part-IX. Synthesis and Antimicrobial Activity of 2-(2'-Aryl-4-thiazolidinon-3'-yl)- 4-(2" -methyl-4" -hydroxy-5"-isopropylphenyl)thiazoles." Journal of Indian Chemical Society Vol. 71, Nov 1994 (1994): 683–85. https://doi.org/10.5281/zenodo.5897621.

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Department of Chemistry, Saurashtra University, Rajkot-360 005 <em>Manuscript received 25 August 1992, revised 7 September 1993, accepted 17 September 1993</em> Several new 4-thiazolidinones have been prepared bearing 2-amino-4-(2&#39;-methyl-4&#39;-hydroxy-5&#39;-isopropylphenyl)thiazole moiety. Their structures have been supported by ir and mass spectral studies. The products have been screened for their antimicrobial activity.
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Book chapters on the topic "Primary Moiety for The Synthesis of Several Antimicrobial"

1

Mellor, Sarah L., and Donald A. Wellings. "Synthesis of modified peptides." In Fmoc Solid Phase Peptide Synthesis. Oxford University Press, 1999. http://dx.doi.org/10.1093/oso/9780199637256.003.0010.

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Several important hormones such as oxytocin, secretin, and LHRH are known to be peptidyl amides. In addition to these, other peptidyl amides such as indolicidin and the protegrins have been shown to exhibit potent antimicrobial activity. The in vivo production of such compounds is via endogenous enzymatic cleavage of propeptides, making their synthesis by genetic engineering notoriously difficult. Furthermore, to facilitate the survival of synthetic peptidyl amides in vivo, an obvious defence against the action of carboxypeptidases is the N-alkylation of the carboxylic amide terminus. Such sec
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