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A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold Научная публикация

Журнал Molecules
, E-ISSN: 1420-3049
Вых. Данные Год: 2018, Том: 23, Номер: 10, Номер статьи : 2468, Страниц : DOI: 10.3390/molecules23102468
Ключевые слова anticancer agent; Tdp1 inhibitor; DNA repair enzyme; synthesis; biochemical assay; molecular modeling; chemical space; structural-activity relationships
Авторы Li-Zhulanov Nikolai S. 1,2,3 , Zakharenko Alexandra L. 4 , Chepanova Arina A. 4 , Patel Jinal 5 , Zafar Ayesha 5 , Volcho Konstantin P. 1,2,3 , Salakhutdinov Nariman F. 1,2,3 , Reynisson Johannes 5 , Leung Ivanhoe K.H. 5 , Lavrik Olga I. 2,3,4
Организации
1 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, 9 Akad Lavrentieva Ave, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Dept Nat Sci, Pirogova 2, Novosibirsk 630090, Russia
3 (Данные Web of science) Novosibirsk State Univ, Inst Med & Psychol, Pirogova 2, Novosibirsk 630090, Russia
4 (Данные Web of science) Russian Acad Sci, Novosibirsk Inst Chem Biol & Fundamental Med, Siberian Branch, 8 Akad Lavrentieva Ave, Novosibirsk 630090, Russia
5 (Данные Web of science) Univ Auckland, Sch Chem Sci, Private Bag 92019,Victoria St West, Auckland 1142, New Zealand

Реферат: Tyrosyl-DNA phosphodiesterase 1 (Tdp1) is a DNA repair enzyme that mends topoisomerase 1-mediated DNA damage. Tdp1 is a current inhibition target for the development of improved anticancer treatments, as its inhibition may enhance the therapeutic effect of topoisomerase 1 poisons. Here, we report a study on the development of a novel class of Tdp1 inhibitors that is based on the octahydro-2H-chromene scaffold. Inhibition and binding assays revealed that these compounds are potent inhibitors of Tdp1, with IC50 and K-D values in the low micromolar concentration range. Molecular modelling predicted plausible conformations of the active ligands, blocking access to the enzymatic machinery of Tdp1. Our results thus help establish a structural-activity relationship for octahydro-2H-chromene-based Tdp1 inhibitors, which will be useful for future Tdp1 inhibitor development work.
Библиографическая ссылка: Li-Zhulanov N.S. , Zakharenko A.L. , Chepanova A.A. , Patel J. , Zafar A. , Volcho K.P. , Salakhutdinov N.F. , Reynisson J. , Leung I.K.H. , Lavrik O.I.
A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold
Molecules. 2018. V.23. N10. 2468 . DOI: 10.3390/molecules23102468 WOS Scopus РИНЦ OpenAlex
Файлы: Полный текст от издателя
Даты:
Опубликована online: 26 сент. 2018 г.
Идентификаторы БД:
Web of science: WOS:000451201400064
Scopus: 2-s2.0-85054090656
РИНЦ: 35788136
OpenAlex: W2893259262
Цитирование в БД:
БД Цитирований
Web of science 31
Scopus 29
РИНЦ 31
OpenAlex 34
Альметрики: