Synthesis of phenylcycloalkylpolycarboxylic acids

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

Synthesis previously undescribed tri- and tetracarboxylic acids containing aromatic and alicyclic fragments. It is known that some compounds with a phenylcycloaliphatic fragment are potential therapeutic agents for the treatment of cancer, Alzheimer’s disease, and some other diseases.

作者简介

A. Firstova

Yaroslavl State Technical University

Email: firstova.a.a@mail.ru

E. Kofanov

Yaroslavl State Technical University

Email: firstova.a.a@mail.ru

参考

  1. Кудрявцев В.А., Хохлова А.В., Мосина В.А., Кабаков А.Е. Радиация и риск. 2016, 25, 57-66.
  2. Kimple R.J. Mol. Interv. 2010, 10, 341-353. doi: 10.1124/mi.10.6.3
  3. Spalding A.C., Lawrence Th.S. Cancer Invest. 2006, 24, 444-456. doi: 10.1080/07357900600705706
  4. Koll T.T., Feis S.S., Wright M.H., Teniola M.M., Richardson M.M., Robles A.I., Bradsher J., Capala J., Varticovski L. Mol. Cancer Ther. 2008, 7, 1985-1992. doi: 10.1158/1535-7163.MCT-07-2104
  5. Dote H., Burgan W.E., Camphausen K., Tofilon J. Cancer Res. 2006, 66, 9211-9220. doi: 10.1158/0008-5472.CAN-06-2181
  6. Kabakov A.E., Kudryavtsev V.A., Gabai V.L. J. Mol. Med. 2010, 88, 241-247. doi: 10.1007/s00109-009-0562-0
  7. Shevtsov M., Multhoff G., Mikhaylova E., Shibata A., Guzhova I., Margulis B. Int. J. Mol. Sci. 2019, 20, 5284-5306. doi: 10.3390/ijms20215284
  8. Trepel J., Mollapour M., Giaccone G., Neckers L. Nat. Rev. Cancer. 2010, 10, 537-549. doi: 10.1038/nrc2887
  9. Jhaveri K., Taldone T., Modi S., Chiosis G. Biochim. Biophys. Acta. 2012, 1823, 742-766. doi: 10.1016/j.bbamcr.2011.10.008
  10. Chaudhury S., Welch T.R., Blagg Br.S.J. ChemMedChem. 2006, 1, 1331-1340. doi: 10.1002/cmdc.200600112
  11. Marcu M.G, Chadli A., Bouhouche I., Catelli M., Neckersi L.M. J. Biol. Chem. 2000, 275, 37181-37186. doi: 10.1074/jbc.M003701200
  12. Burlison J.A., Neckers L., Smith A.B., Maxwell A., Blagg Br.S.J. J. Am. Chem. Soc. 2006, 128, 15529-15536. doi: 10.1021/ja065793p
  13. Zhao H., Moroni E., Colombo G., Blagg Br.S.J. ACS Med. Chem. Lett. 2014, 5, 84-88. doi: 10.1021/ml400404s
  14. Zhao J., Zhao H., Hall J.A., Brown D., Brandes E., Bazzill J., Grogan P.T., Subramanian Ch., Vielhauer G., Cohen M.S., Blagg Br.S.J. Med. Chem. Commun. 2014, 5, 1317-1323. doi: 10.1039/C4MD00102H
  15. Bishop S.C., Burlison J.A., Blagg Br.S.J. Curr. Cancer Drug Targets. 2007, 7, 369-388. doi: 10.2174/156800907780809778
  16. Garg G., Forsberg L.K., Zhao H., Blagg Br.S.J. Chemistry. 2017, 23, 16574-16585. doi: 10.1002/chem.201703206
  17. Solit D.B., Chiosis G. Drug Dis. Today. 2008, 13, 38-43. doi: 10.1016/j.drudis.2007.10.007
  18. Neckers L., Workman P. Clin Cancer Res. 2012, 18, 64-76. doi: 10.1158/1078-0432.CCR-11-1000
  19. Garg G., Zhao H., Blagg B.S.J. Bioorg. Med. Chem. 2017, 25, 451-457. doi: 10.1016/j.bmc.2016.11.030
  20. Tikhonova T.B., Barygin O.I., Gmiro V.E., Tikhonov D.B., Magazanik L.G. Neuropharmacology. 2008, 54, 653-664. doi: 10.1016/j.neuropharm.2007.11.014
  21. Lukomskaya N.Ya., Lavrent'eva V.V., Starshinova L.A., Zhabko E.P., Gmiro V.E., Magazanik L.G. Neurosci. Behav. Physiol. 2008, 38, 421-426. doi: 10.1007/s11055-008-0060-9
  22. Dey S., Temme L., Schreiber J.A., Schepmann D., Frehland B., Lehmkuhl K., Strutz-Seebohm N., Seebohm G., Wünsch B. Eur. J. Med. Chem. 2017, 138, 552-564. doi: 10.1016/j.ejmech.2017.06.068
  23. Tan B.-H., Yoshikai N. Org. Lett. 2014, 16, 3392-3395. doi: 10.1021/ol501449j
  24. Bartoli G., Cacchi S., Fabrizi G., Goggiamani A. Synlett. 2008, 16, 2508-2512. doi: 10.1055/s-2008-1078051
  25. Фирстова А.А., Кофанов Е.Р., Красовская Г.Г., Данилова А.С. Изв. АН. Сер. хим. 2017, 66, 867-869.
  26. Firstova A.A., Kofanov E.R., Krasovskaya G.G., Danilova A.S. Russ. Chem. Bull. 2017, 66, 867-869. doi: 10.1007/s11172-017-1820-x
  27. Травень В.Ф. Органическая химия: учебник для вузов в 2 т. М.: ИКЦ "Академкнига", 2004, 427-428.
  28. Sugita K., Tamura S. Bull. Chem. Soc. Jpn. 1971, 44, 3388-3391. doi: 10.1246/bcsj.44.2866
  29. Колобов А.В., Борисов П.В. Изв. вузов. Сер. хим. и хим. техн. 2007, 50, 59-61.
  30. Stájer G., Virág M., Szabo A.E. Acta Chem. Scand. 1996, 50, 922-930. doi: 10.3891/acta.chem.scand.50-0922
  31. Krasnikov S.V., Obuchova T.A., Yasinskii O.A., Balakin K.V. Tetrahedron Lett. 2004, 45, 711-714. doi: 10.1016/j.tetlet.2003.11.057
  32. Бетнев А.Ф., Обухова Т.А., Клюев И.В., Красников С.В. Изв. Вузов. Сер. хим. и хим. техн. 2000, 43, 73-75.
  33. Hirashima I., Itoh A. Synth. 2006, 11, 1757-1759. doi: 10.1055/s-2006-942356
  34. Sugai T., Itoh A.Tetrahedron Lett. 2007, 48, 2931-2934. doi: 10.1016/j.tetlet.2007.02.060
  35. Tada N., Hattori K., Nobuta T., Miura T., Itoh A. Green Chem. 2011, 13, 1669-1671. doi: 10.1039/C1GC15154A
  36. Беккер Х., Бергер В., Домшке Г. Органикум. М.: Мир. 1992, 2, 62-69.
  37. McDougall F.H. J. Am. Chem. Soc. 1936, 58, 2585-2591. doi: 10.1021/ja01303a060

补充文件

附件文件
动作
1. JATS XML
下载

版权所有 © Russian Academy of Sciences, 2023