Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties | Sciact - CRIS-система Института катализа

Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties Научная публикация

Журнал

Pharmaceuticals
ISSN: 1424-8247

Вых. Данные

Год: 2021, Том: 14, Номер: 5, Номер статьи : 422, Страниц : 17 DOI: 10.3390/ph14050422

Ключевые слова

Adamantane; Resin acid; TDP1; Tyrosil-DNA-phosphodiesterase 1

Авторы

Kovaleva Kseniya ¹ , Yarovaya Olga ^1,2 , Ponomarev Konstantin ¹ , Cheresiz Sergey ² , Azimirad Amirhossein ² , Chernyshova Irina ² , Zakharenko Alexandra ³ , Konev Vasily ⁴ , Khlebnikova Tatiana ⁴ , Mozhaytsev Evgenii ¹ , Suslov Evgenii ¹ , Nilov Dmitry ⁵ , Švedas Vytas ^5,6 , Pokrovsky Andrey ² , Lavrik Olga ^2,3 , Salakhutdinov Nariman ¹

Организации

1	N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Lavrentiev Ave. 9, 630090 Novosibirsk, Russia
2	V. Zelman Institute for the Medicine and Psychology, Novosibirsk State University, Pirogova St. 1, 630090 Novosibirsk, Russia
3	Novosibirsk Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Lavrentiev Ave. 8, 630090 Novosibirsk, Russia
4	Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Lavrentiev Ave. 5, Novosibirsk, 630090, Russian Federation
5	Belozersky Institute of Physicochemical Biology, Lomonosov Moscow State University, Lenin Hills 1, Bldg. 40, 119991 Moscow, Russia
6	Faculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Lenin Hills 1, Bldg. 73, 119991 Moscow, Russia

Информация о финансировании (1)

Российский научный фонд

19-73-00051

In this paper, a series of novel abietyl and dehydroabietyl ureas, thioureas, amides, and thioamides bearing adamantane moieties were designed, synthesized, and evaluated for their in-hibitory activities against tyrosil-DNA-phosphodiesterase 1 (TDP1). The synthesized compounds were able to inhibit TDP1 at micromolar concentrations (0.19–2.3 µM) and demonstrated low cytotox-icity in the T98G glioma cell line. The effect of the terpene fragment, the linker structure, and the adamantane residue on the biological properties of the new compounds was investigated. Based on molecular docking results, we suppose that adamantane derivatives of resin acids bind to the TDP1 covalent intermediate, forming a hydrogen bond with Ser463 and hydrophobic contacts with the Phe259 and Trp590 residues and the oligonucleotide fragment of the substrate. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Kovaleva K. , Yarovaya O. , Ponomarev K. , Cheresiz S. , Azimirad A. , Chernyshova I. , Zakharenko A. , Konev V. , Khlebnikova T. , Mozhaytsev E. , Suslov E. , Nilov D. , Švedas V. , Pokrovsky A. , Lavrik O. , Salakhutdinov N.
Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties

Pharmaceuticals. 2021. V.14. N5. 422 :1-17. DOI: 10.3390/ph14050422 WOS Scopus РИНЦ CAPlusCA PMID OpenAlex

Полный текст от издателя

Поступила в редакцию:	26 мар. 2021 г.
Принята к публикации:	23 апр. 2021 г.
Опубликована в печати:	1 мая 2021 г.
Опубликована online:	1 мая 2021 г.

Web of science:	WOS:000654404200001
Scopus:	2-s2.0-85105952939
РИНЦ:	46067043
Chemical Abstracts:	2021:1294327
Chemical Abstracts (print):	175:266614
PMID (PubMed):	34062881
OpenAlex:	W3158355266

БД	Цитирований
Scopus	12
Web of science	12
РИНЦ	13
OpenAlex	12