Synthesis and biological evaluation of alkali metal salts of tryptanthrin-6-oxime; 53rd International Union of Pure & Applied Chemistry General Assembly (IUPAC 2025) and 50th World Chemistry Congress (50WCC)

Библиографические подробности
Источник:53rd International Union of Pure & Applied Chemistry General Assembly (IUPAC 2025) and 50th World Chemistry Congress (50WCC).— 2025.— P. 210
Главный автор: Kovrizhina A. R. Anastasia Ruslanovna
Другие авторы: Khlebnikov A. I. Andrey Ivanovich, Plotnikov E. V. Evgeny Vladimirovich
Примечания:Title screen
Indolo[2,1-b]quinazolin-6,12-dione oxime (tryptanthrin-6-oxime, Tryp-Ox) exhibit a variety of chemical properties and pharmacological activities. Owing to ion-chelating properties, oximes can be ligands in various complexes formed by metal ions. As the complex formation can affect biological activity of oximes, we decided to obtain a series of alkali metal salts (oximates) containing the Tryp-Ox scaffold (Figure 1) and study their solubility and cytotoxicity. Previously we synthesized lithium and sodium salts of Tryp-Ox and established their high affinity for JNK1-3 (Kd < 1 μM) and potent inhibition of LPS-induced nuclear NF-κB/AP-1 activation and IL-6 production in human monocytic cells [1]. The c-Jun N-terminal kinase (JNK) pathway is a dual-functional oncogenic signaling that exerts both anti- and pro-tumor activities [2,3]. In this research we focused on evaluation the antitumor activity of oximates
Текстовый файл
Язык:английский
Опубликовано: 2025
Предметы:
Online-ссылка:https://iupac-2025.s3.ap-southeast-1.amazonaws.com/j3y8n5cpauaosv9ekold8novsqtj#page=210
Формат: Электронный ресурс Статья
Запись в KOHA:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=682288

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330 |a Indolo[2,1-b]quinazolin-6,12-dione oxime (tryptanthrin-6-oxime, Tryp-Ox) exhibit a variety of chemical properties and pharmacological activities. Owing to ion-chelating properties, oximes can be ligands in various complexes formed by metal ions. As the complex formation can affect biological activity of oximes, we decided to obtain a series of alkali metal salts (oximates) containing the Tryp-Ox scaffold (Figure 1) and study their solubility and cytotoxicity. Previously we synthesized lithium and sodium salts of Tryp-Ox and established their high affinity for JNK1-3 (Kd < 1 μM) and potent inhibition of LPS-induced nuclear NF-κB/AP-1 activation and IL-6 production in human monocytic cells [1]. The c-Jun N-terminal kinase (JNK) pathway is a dual-functional oncogenic signaling that exerts both anti- and pro-tumor activities [2,3]. In this research we focused on evaluation the antitumor activity of oximates 
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463 1 |t 53rd International Union of Pure & Applied Chemistry General Assembly (IUPAC 2025) and 50th World Chemistry Congress (50WCC)  |o e-Abstract Book, Kuala Lumpur, Malaysia, 12-16 July 2025 and 14-19 July 2025  |c Bandar Bangi   |n National University of Malaysia  |d 2025  |v P. 210  |y 978-5-4437-1350-2 
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700 1 |a Kovrizhina  |b A. R.  |c biotechnology specialist  |c Research Engineer of Tomsk Polytechnic University  |f 1995-  |g Anastasia Ruslanovna  |9 22266 
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701 1 |a Plotnikov  |b E. V.  |c chemist  |c Associate Professor of Tomsk Polytechnic University, Candidate of Chemical Sciences  |f 1983-  |g Evgeny Vladimirovich  |9 16417 
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