Abstract: A series of deoxycholic acid (DCA) amides containing benzyl ether groups on the steroid core were tested against the tyrosyl-DNA phosphodiesterase 1 (TDP1) and 2 (TDP2) enzymes. In addition, 1,2,4-and 1,3,4-oxadiazole derivatives were synthesized to study the linker influence between a para-bromophenyl moiety and the steroid scaffold. The DCA derivatives demonstrated promising inhibitory activity against TDP1 with IC50 in the submicromolar range. Furthermore, the amides and the 1,3,4-oxadiazole derivatives inhibited the TDP2 enzyme but at substantially higher concentration. Tryptamide 5 and para-bromoanilide 8 derivatives containing benzyloxy substituent at the C-3 position and non-substituted hydroxy group at C-12 on the DCA scaffold inhibited both TDP1 and TDP2 as well as enhanced the cytotoxicity of topotecan in non-toxic concentration in vitro. According to molecular modeling, ligand 5 is anchored into the catalytic pocket of TDP1 by one hydrogen bond to the backbone of Gly458 as well as by π–π stacking between the indolyl rings of the ligand and Tyr590, resulting in excellent activity. It can therefore be concluded that these derivatives contribute to the development of specific TDP1 and TDP2 inhibitors for adjuvant therapy against cancer in combination with topoisomerase poisons. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Cite: Salomatina O.V. , Dyrkheeva N.S. , Popadyuk I.I. , Zakharenko A.L. , Ilina E.S. , Komarova N.I. , Reynisson J. , Salakhutdinov N.F. , Lavrik O.I. , Volcho K.P.
New deoxycholic acid derived tyrosyl-dna phosphodiesterase 1 inhibitors also inhibit tyrosyl-dna phosphodiesterase 2
Molecules. 2022. V.27. N1. 72 . DOI: 10.3390/molecules27010072 WOS Scopus РИНЦ OpenAlex

Dates:

Submitted:	Nov 18, 2021
Accepted:	Dec 21, 2021
Published online:	Dec 23, 2021

Identifiers:

Web of science:	WOS:000741699500001
Scopus:	2-s2.0-85121745314
Elibrary:	47549342
OpenAlex:	W4200404596

Citing:

DB	Citing
Scopus	7
Elibrary	7
Web of science	10
OpenAlex	12

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