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Novel PARP1 inhibitors potentiate doxorubicin antitumor activity in vitro Научная публикация

Журнал Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Вых. Данные Год: 2015, Том: 25, Номер: 5, Страницы: 364-366 Страниц : 3 DOI: 10.1016/j.mencom.2015.09.016
Авторы Rakitina Tatiana V. 1,2 , Zeifman Alexey A. 3 , Novikov Fedor N. 3 , Stroganov Oleg V. 3 , Stroylov Victor S. 3 , Svitanko Igor V. 3,4 , Frank-Kamenetskii Anastasia 1 , Chilov Ghermes G. 3
Организации
1 National Research Centre ‘Kurchatov Institute’, 123182 Moscow, Russian Federation
2 M. M. Shemyakin–Yu. A. Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russian Federation.
3 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation
4 Department of Chemistry, M. V. Lomonosov Moscow State University, 119991 Moscow, Russian Federation

Реферат: Six novel potential PARP1 inhibitors were identified by means of substructure search and molecular docking into PAPR1 active site; one compound (STK970217) potentiated the cytotoxicity of doxorubicin in hepatocellular carcinoma HepG2 cells being non-cytotoxic as a single agent, while three other identified compounds inhibited the growth of HepG2 cells both individually and in combination with doxorubicin.
Библиографическая ссылка: Rakitina T.V. , Zeifman A.A. , Novikov F.N. , Stroganov O.V. , Stroylov V.S. , Svitanko I.V. , Frank-Kamenetskii A. , Chilov G.G.
Novel PARP1 inhibitors potentiate doxorubicin antitumor activity in vitro
Mendeleev Communications. 2015. V.25. N5. P.364-366. DOI: 10.1016/j.mencom.2015.09.016 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000363350500016
Scopus: 2-s2.0-84943261323
OpenAlex: W1878296260
Цитирование в БД:
БД Цитирований
OpenAlex 4
Scopus 4
Web of science 4
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