Synthesis and cytotoxic activity evaluation of maleopimaric and dihydroquinopimaric esters and amides

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

The new 1-, 1,4- and 1,4,20-diethoxyphosphoryl-containing esters were synthesized as a result of interaction of dihydroquinopimaric acid methyl ester hydroxyl derivatives with diethylchlorophosphite, A study of the cytotoxic activity in vitro on 60 cell lines of nine different human tumors of methyl ester of dihydroquinopimaric acid with diethoxyphosphoryl, furan and indole fragments, as well as diterpene amides with linear, heterocyclic and aromatic amines residues showed that diethoxyphosphoryl and benzylamine substituents are of key importance for the manifestation of the cytotoxic effect. Diethoxyphosphoryl derivatives (XIX) and (XVII), and benzylamide (IX) showed cytotoxic activity against one, seven and four cell lines of breast cancer, leukemia, non-small cell lung cancer, melanoma and prostate cancer, respectively. The greatest activity was demonstrated by maleopimaric acid benzylamide (XIII), which effectively inhibited the growth of 19 cell lines of eight cancer types and had a significant cytotoxic effect against all studied leukemia cell lines.

全文:

受限制的访问

作者简介

E. Tretyakova

Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: tretyakovaelv@gmail.com
俄罗斯联邦, prosp. Oktyabrya 71, Ufa, 450054

S. Sharafutdinova

Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences; Ufa University of Science and Technology

Email: tretyakovaelv@gmail.com
俄罗斯联邦, prosp. Oktyabrya 71, Ufa, 450054; Ufa, ul. Zaki Validi 32, 450076

参考

  1. Wiemann J., Al-Harrasi A., Csuk R. // Anticancer Agents Med. Chem. 2020. V. 20. P. 1756–1767. https://doi.org/10.2174/1871520620666200317110010
  2. Tretyakova E.V., Smirnova I.E., Kazakova O.B., Tolstikov G.A., Yavorskaya N.P., Golubeva I.S., Pugacheva R.B., Apryshko G.N., Poroikov V.V. // Bioorg. Med. Chem. 2014. V. 22. P. 6481–6489. https://doi.org/10.1016/j.bmc.2014.09.030
  3. Ahmad B., Tian C., Tang J.-X., Dumbuya J.S., Li W., Lu J. // Front. Pharmacol. 2024. V. 15. P. 1392203. https://doi.org/10.3389/fphar.2024.1392203
  4. Haffez H., Osman S., Ebrahim H.Y., Hassan Z.A. // Molecules. 2022. V. 27. P. 293. https://doi.org/10.3390/molecules27010293
  5. Liu X., Chen W., Liu Q., Dai J. // Onco Targets Ther. 2019. V. 12. P. 4825–4837. https://doi.org/10.2147/OTT.S199161
  6. Xu Y., Tong Y., Lei Z., Zhu J., Wan L. // Biomed. Pharmacother. 2023. V. 158. P. 114154. https://doi.org/10.1016/j.biopha.2022.114154
  7. Lin C.H., Chuang H.S. // Patent US7015248B2, published 01.04.2004.
  8. Tanaka R., Tokuda H., Ezaki Y. // Phytomedicine. 2008. V. 15. P. 985–992. https://doi.org/10.1016/j.phymed.2008.02.020
  9. Yoshida N., Takada T., Yamamura Y., Adachi I., Suzuki H., Kawakami J. // Drug Metab. Dispos. 2008. V. 36. P. 1206–1211. https://doi.org/10.1124/dmd.107.019513
  10. Hsieh Y.S., Yang S.F., Hsieh Y.H., Hung C. H., Chu S.C., Yang S.H., Chen P.N. // Am. J. Chin. Med. 2015. V. 43. P. 1697–1714. https://doi.org/10.1142/S0192415X15500962
  11. Kazakova O.B., Smirnova I.E., Do Tkhi Tkhu Kh, Tkhankh Tra Nguen, Apryshko G.N., Zhukova O.S., Medvedeva N.I., Nazyrov T.I., Tret’iakova E.V., Chudov I.V., Ismagilova A.F., Suponitskii K.Iu., Kazakov D.V., Safarov F.E., Tolstikov G.A. // Russ. J. Bioorg. Chem. 2013. V. 39. P. 202–210. https://doi.org/10.1134/s1068162013020088.
  12. Tret’yakova E.V., Zakirova G.F., Salimova E.V., Kukovinets O.S., Odinokov V.N., Parfenova L.V. // Med. Chem. Res. 2018. V. 27. P. 2199–2213. https://doi.org/10.1007/s00044-018-2227-4
  13. Smirnova A.A., Zakirova L.M., Smirnova I.E., Tretyakova E.V. // Molbank. 2023. V. 2023. P. M1707. https://doi.org/10.3390/M1707
  14. Tretyakova E.V., Salimova E.V., Parfenova L.V., Yunusbaeva M.M., Dzhemileva L.U., D’yakonov V.V., Dzhemilev U.M. // Anticancer Agents Med. Chem. 2019. V. 19. P. 1172–1183. https://doi.org/10.2174/1871520619666190404100846
  15. Tret’yakova E.V., Salimova E.V., Parfenova L.V. // Nat. Prod. Res. 2020. V. 36. P. 79–86. https://doi.org/10.1080/14786419.2020.1762187
  16. Tretyakova E., Heise N.V., Csuk R., Kazakova O. // Nat. Prod. Res. 2023. P. 1–9. https://doi.org/10.1080/14786419.2023.2266107
  17. Smirnova I.E., Tret’yakova E.V., Baev D.S., Kazakova O.B. // Nat. Prod. Res. 2023. V. 37. P. 313–321. https://doi.org/10.1080/14786419.2021.1969566
  18. Zielonka J., Josep J., Sikora A., Hardy M., Ouari O., Vasquez-Vivar J., Cheng G., Lopez M., Kalyanaraman B. // Chem. Rev. 2017. V. 117. P. 10043–10120. https://doi.org/10.1021/acs.chemrev.7b00042
  19. Chrobak E., Bębenek E., Kadela-Tomanek M., Latocha M., Jelsch C., Wenger E., Boryczka S. // Molecules. 2016. V. 21. P. 1123. https://doi.org/10.3390/molecules21091123
  20. Abdou W.M., Shaddy A.A. // Arkivoc. 2009. P. 143–182. https://doi.org/10.3998/ark.5550190.0010.910
  21. Spivak A.Y., Nedopekina D.A., Shakurova E.R., Khalitova R.R., Gubaidullin R.R., Odinokov V.N., Dzhemilev U.M., Bel’skii Y.P., Bel’skaya N.V., Stankevich S.A., Korotkaya E.V., Khazanov V.A. // Russ. Chem. Bull. 2013. V. 62. P. 188–198. https://doi.org/10.1007/s11172-013-0028-y
  22. Спивак А.Ю., Халитова Р.Р., Шакурова Э.Р., Недопекина Д.А., Губайдуллин Р.Р., Одиноков В.Н., Джемилев У.М., Бельский Ю.П., Бельская Н.В., Станкевич С.А., Хазанов В.А. // Патент RU2551647C2, опубл. 27.05.2015.
  23. Кайзер Д., Спивак А.Ю., Недопекина Д.А., Губайдуллин Р.Р., Одиноков В.Н., Джемилев У.М., Бельский Ю.П., Бельская Н.В., Станкевич С.А., Хазанов В.А. // Патент RU2576658C2, опубл. 10.03.2016.
  24. Shinkareva A.M., Nemtarev A.V., Chachkov D.V., Dobrynin A.B., Litvinov I.A., Mironov V.F. // Mend. Commun. 2024. V. 34. P. 113–115. https://doi.org/10.1016/j.mencom.2024.01.034
  25. Smirnova I.E., Tret’yakova E.V., Flekhter O.B., Spirikhin L.V., Galin F.Z., Tolstikov G.A., Starikova Z.A., Korlyukov A.A. // Russ. J. Org. Chem. 2008. V. 44. P. 1598–1605. https://doi.org/10.1134/S1070428008110055
  26. Vafina G.F., Khanova M.D., Meshcheryakova S.A., Bulgakov A.K. // Chem. Nat. Compd. 2019. V. 55. P. 868–870. https://doi.org/10.1007/s10600-019-02835-z
  27. NCI-60 Screening Methodology // National Cancer Institute. Developmental Therapeutics Program. https://dtp.cancer.gov/discovery_development/nci-60/methodology.htm
  28. Grever M.R., Schepartz S.A., Chabner B.A. // Semin. Oncol. 1992. V. 19. P. 622–638.
  29. Boyd M.R., Paull K.D. // Drug Dev. Res. 1995. V. 34. P. 91–109. https://doi.org/10.1002/ddr.430340203
  30. Shoemaker R.H. // Nature Rev. 2006. V. 6. P. 813–823. https://doi.org/10.1038/nrc1951

补充文件

附件文件
动作
1. JATS XML
下载
2. Fig. 1. Methyl dihydroquinopimarate esters (I–V) [16] and amides of dihydroquinopimaric (VI–IX) and maleopimaric (X–XIII) acids [17]. Reagents and conditions: (EtO)2POCl, DMAP, pyridine, 0–23°C, 3 h.

下载 (117KB)
索引源数据
3. Scheme 1. Synthesis of diethoxyphosphoryl derivatives (XVII–XIX).

下载 (113KB)
索引源数据

版权所有 © Russian Academy of Sciences, 2024