Synthesis and Biological Activity of New Hydrazones Based on N-Aminomorpholine

التفاصيل البيبلوغرافية
Parent link:Molecules.— .— Basel: MDPI AG
Vol. 29, iss. 15.— 2024.— Article number 3606, 14 p.
مؤلفون آخرون: Nurkenov O. A. Oralgazy, Zhautikova S. B. Saule, Khlebnikov A. I. Andrey Ivanovich, Syzdykov A. K. Ardak, Fazylov S. D. Serik, Seilkhanov T. M. Tulegen, Kabieva S. K. Saule, Turdybekov K. M. Kobylandy, Mendibayeva A. Z. Anel, Zhumanazarova G. M. Gaziza
الملخص:Title screen
The data on the synthesis of N-aminomorpholine hydrazones are presented. It is shown that the interaction of N-aminomorpholine with functionally substituted benzaldehydes and 4-pyridinaldehyde in isopropyl alcohol leads to the formation of corresponding hydrazones. The structure of the synthesized compounds was studied by 1H and 13C NMR spectroscopy methods, including the COSY (1H-1H), HMQC (1H-13C) and HMBC (1H-13C) methodologies. The values of chemical shifts, multiplicity, and integral intensity of 1H and 13C signals in one-dimensional NMR spectra were determined. The COSY (1H-1H), HMQC (1H-13C), and HMBC (1H-13C) results revealed homo- and heteronuclear interactions, confirming the structure of the studied compounds. The antiviral, cytotoxic, and antimicrobial activity of some synthesized hydrazones were investigated. It is shown that 2-((morpholinoimino)methyl)benzoic acid has a pronounced viral inhibitory property, comparable in its activity to commercial drugs Tamiflu and Remantadine. A docking study was performed using the influenza virus protein models (1930 Swine H1 Hemagglutinin and Neuraminidase of 1918 H1N1 strain). The potential binding sites that are complementary with 2-((morpholinoimino)methyl)benzoic acid were found
Текстовый файл
اللغة:الإنجليزية
منشور في: 2024
الموضوعات:
الوصول للمادة أونلاين:https://doi.org/10.3390/molecules29153606
التنسيق: الكتروني فصل الكتاب
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=678075

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330 |a The data on the synthesis of N-aminomorpholine hydrazones are presented. It is shown that the interaction of N-aminomorpholine with functionally substituted benzaldehydes and 4-pyridinaldehyde in isopropyl alcohol leads to the formation of corresponding hydrazones. The structure of the synthesized compounds was studied by 1H and 13C NMR spectroscopy methods, including the COSY (1H-1H), HMQC (1H-13C) and HMBC (1H-13C) methodologies. The values of chemical shifts, multiplicity, and integral intensity of 1H and 13C signals in one-dimensional NMR spectra were determined. The COSY (1H-1H), HMQC (1H-13C), and HMBC (1H-13C) results revealed homo- and heteronuclear interactions, confirming the structure of the studied compounds. The antiviral, cytotoxic, and antimicrobial activity of some synthesized hydrazones were investigated. It is shown that 2-((morpholinoimino)methyl)benzoic acid has a pronounced viral inhibitory property, comparable in its activity to commercial drugs Tamiflu and Remantadine. A docking study was performed using the influenza virus protein models (1930 Swine H1 Hemagglutinin and Neuraminidase of 1918 H1N1 strain). The potential binding sites that are complementary with 2-((morpholinoimino)methyl)benzoic acid were found 
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463 1 |t Vol. 29, iss. 15  |v Article number 3606, 14 p.  |d 2024 
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610 1 |a o-formyl benzoic acid 
610 1 |a 3-acetoxy-isoindolin-1-ones 
610 1 |a NMR spectroscopy 
610 1 |a antiviral activity 
610 1 |a molecular modeling 
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701 1 |a Zhautikova  |b S. B.  |g Saule 
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701 1 |a Fazylov  |b S. D.  |g Serik 
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701 1 |a Turdybekov  |b K. M.  |g Kobylandy 
701 1 |a Mendibayeva  |b A. Z.  |g Anel 
701 1 |a Zhumanazarova  |b G. M.  |g Gaziza 
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