Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/ apyrimidinic endonuclease 1 and DNA polymerase β

Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/ apyrimidinic endonuclease 1 and DNA polymerase β Научная публикация

Журнал

Biopolymers and Cell
ISSN: 0233-7657

Вых. Данные

Год: 2012, Том: 28, Номер: 3, Страницы: 223-228 Страниц : 6 DOI: 10.7124/bc.000052

Ключевые слова

Apurinic/apyrimidinic endonuclease 1; DNA polymerase β; Glycyrrhetinic acid; Inhibitor; Poly(ADP-ribose)polymerases 1 and 2

Авторы

Zakharenko A.L. ¹ , Salomatina O.V. ² , Sukhanova M.V. ¹ , Kutuzov M.M. ¹ , Ilina E.S. ¹ , Khodyreva S.N. ¹ , Schreiber V. ³ , Salakhutdinov N.F. ² , Lavrik O.I. ¹

Организации

1	(Scopus) Novosibirsk Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, 8, Akademika Lavrentieva Ave, Novosibirsk, 630090, Russian Federation
2	(Scopus) N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9, Akademika Lavrentieva Ave, Novosibirsk, 630090, Russian Federation
3	(Scopus) UMR7242, University of Strasbourg, CNRS, ESBS, Cedex Illkirch Cedex, 67412, France

For strengthening the efficiency of monofunctional alkylating antineoplastic drugs it is important to lower the capacity of base excision repair (BER).system which corrects the majority of DNA damages caused by these reagents. The objective was to create inhibitors of the key BER enzymes (PARP1, PARP2, DNA polymerase β, and APE1) by the directed modification of glycyrrhetinic acid (GA). Methods. Amides of GA were produced from the GA acetate byformation of the corresponding acyl chloride, amidation with the appropriate amine and subsequent deacylation. Small library of 2-cyano substituted derivatives of GA methyl esters was obtained by the structural modification of GA framework and carboxylic acid group. The inhibitory capacity of the compounds was estimated by comparison of the enzyme activities in specific tests in the presence of compounds versus their absence. Results. None of tested compounds inhibits PARP1 significantly. Unmodified GA and its morpholinic derivative were shown to be weak inhibitors of PARP2. The derivatives of GA containing keto-group in 11 triterpene framework were shown to be moderate inhibitors of pol β. Compound3, containing 12-oxo-9(11)-en moiety in the ring C, was shown to be a single inhibitor of APE1 among all compounds studied. Conclusions. The class of GA derivatives, selective pol β inhibitors, was found out. The selective inhibitor of APE 1 and weak selective inhibitor of PARP2 were also revealed. © Institute of Molecular Biology and Genetics, NAS of Ukraine, 2012.

Zakharenko A.L. , Salomatina O.V. , Sukhanova M.V. , Kutuzov M.M. , Ilina E.S. , Khodyreva S.N. , Schreiber V. , Salakhutdinov N.F. , Lavrik O.I.
Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/ apyrimidinic endonuclease 1 and DNA polymerase β

Biopolymers and Cell. 2012. V.28. N3. P.223-228. DOI: 10.7124/bc.000052 Scopus РИНЦ

Полный текст от издателя

Опубликована в печати:

20 мая 2012 г.

Scopus	2-s2.0-84863806118
РИНЦ	17840833
OpenAlex	W2334572009