Метод получения новых о-ацилоксимов триптантрина

Bibliographic Details
Parent link:Перспективы развития фундаментальных наук=Prospects of Fundamental Sciences Development: сборник научных трудов XVIII Международной конференции студентов, аспирантов и молодых ученых, г. Томск, 27-30 апреля 2021 г./ Национальный исследовательский Томский политехнический университет (ТПУ) ; под ред. И. А. Курзиной, Г. А. Вороновой.— , 2021
Т. 2 : Химия.— 2021.— [С. 134-136]
Main Author: Кузнецов А. А.
Corporate Author: Национальный исследовательский Томский политехнический университет Инженерная школа новых производственных технологий Научно-образовательный центр Н. М. Кижнера
Other Authors: Коврижина А. Р. Анастасия Руслановна (727), Хлебников А. И. Андрей Иванович
Summary:Заглавие с экрана
Earlier [1, 2], a number of new potential inhibitors of the JNK kinase isoform family (JNK1, JNK2, JNK3) were identified, which are involved in the pathogenesis of many cardiovascular, oncological and psychosomatic diseases. One of the potential inhibitors is tryptanthrin-6-oxime (Trp-Ox), which exhibit good pan-selectivity for JNK. However, most of the compounds had low solubility in water and organic solvents and high toxicity. This work presents the synthesis of new tryptanthrin O-acyloximes with the aim of increasing their activity and / or the selectivity of the obtained analogs with respect to JNK isoforms, their hydrophilic properties and expanding the library of nitrogen-containing heterocyclic compounds, which will also be of interest to researchers studying other type biological activity.
Published: 2021
Subjects:
Online Access:http://earchive.tpu.ru/handle/11683/68297
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=633343