- PII
- S30346304S0514749225030037-1
- DOI
- 10.7868/S3034630425030037
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 61 / Issue number 3
- Pages
- 240-245
- Abstract
- A convenient synthetic approach to the synthesis of new 2-R-6Н-benzopyrano[4,3-е][1,2,4]triazolo[5,1-с][1,2,4]triazin-6-ones and 2-R-[1,2,4]triazolo[5',1':3,4][1,2,4]triazino[6,5-c]quinolin-6(7H)-ones based on 3-R-1H-1,2,4-triazolo-5-diazonium salts with 2H-1-benzopyran-2,4(3H)dione and 2,4(1H,3H)-quinolinedione.
- Keywords
- 1H-1,2,4-триазоло-5-диазониевые соли 2Н-1-бензопиран-2,4(3Н)дион 2,4(1Н,3Н)-хинолиндион гидразоны 6Н-бензопирано[4,3-е][1,2,4]триазоло[5,1-с][1,2,4]триазин-6-оны [1,2,4]триазоло[5',1':3,4][1,2,4]триазино[6,5-c]хинолин-6(7H)-оны
- Date of publication
- 23.03.2023
- Year of publication
- 2023
- Number of purchasers
- 0
- Views
- 19
References
- 1. Viegas-Junior C., Danuello A., da Silva Bolzani V., Barreiro E.J., Manssour Fraga C.A. Curr. Med. Chem. 2007, 14, 1829-1852. doi 10.2174/092986707781058805
- 2. Gao F., Ye L., Wang Y., Kong F., Zhao Sh., Xiao J., Huang G. Eur. J. Med. Chem. 2019, 183, 111678. doi 10.1016/j.ejmech.2019.111678
- 3. Meunier B. Acc. Chem. Res. 2008, 41, 69-77. doi 10.1021/ar7000843
- 4. Kartsev V., Shikhaliev Kh.S., Geronikaki A., Medvedva S.M., Ledenyova I.V., Krysin M.Yu., Petrou A., Ciric A., Glamoclija J., Sokovic M. Eur. J. Med. Chem. 2019, 175, 201-214. doi 10.1016/j.ejmech.2019.04.046
- 5. Gao J., Zhang, Z., Zhang B., Mao Q., Dai X., Zou Q., Lei Y., Feng Y., Wang S. Bioorg. Chem. 2020, 95, 103564. doi 10.1016/j.bioorg.2019.103564
- 6. Novichikhina N., Ilin I., Tashchilova A., Sulimov A., Kutov D., Ledenyova I., Krysin M., Shikhaliev Kh., Gantseva A., Gantseva E., Podoplelova N., Sulimov V. Molecules 2020, 25, 1889. doi 10.3390/molecules25081889
- 7. Djemoui A., Naouri A., Ouahrani M.R., Djemoui D., Lahcene S., Lahrech M.B., Boukenna L., Albuquerque H.M.T., Saher L., Rocha D.H.A., Monteiro F.L., Helguero L.A., Bachari K., Talhi O., Silva A.M.S. J. Mol. Struct. 2020, 1204, 127487. doi 10.1016/j.molstruc.2019.127487
- 8. Новичихина Н.П., Шестаков А.С., Потапов А.Ю., Кошелева Е.А., Шаталов Г.В., Вережников В.Н., Вандышев Д.Ю., Леденева И.В., Шихалиев Х.С. Изв. А.Н. Сер. хим. 2020, № 4, 787-792.
- 9. Novichikhina N.P., Shestakov A.S., Potapov A.Yu.,. Kosheleva E.A, Shatalov G.V., Verezhnikov V.N., Vandyshev D.Yu., Ledeneva I.V., Shikhaliev Kh.S. Russ. Chem. Bull. 2020, № 4, 787-792
- 10. Welsch M.E., Snyder S.A., Stockwell B.R. Curr. Opin. Chem. Biol. 2010, 14, 347-361. doi 10.1016/j.cbpa.2010.02.018
- 11. DeSimone R.W., Currie K.S., Mitchell S.A., Darrow J.W., Pippin D.A. Comb. Chem. High Throughput Screen 2004, 7, 473-494. doi 10.2174/1386207043328544
- 12. Sarveswari S., Vijayakumar V., Siva R., Priya R. Appl. Biochem. Biotechnol. 2015, 175 (1), 43-64. doi 10.1007/s12010-014-1256-9
- 13. Sabbah D.A., Hishmah B., Sweidan K., Bardaweel S., AlDamen M., Zhong H.A., Khalaf R.A., Ameerah (Hasan Ibrahim), Al-Qirim T., Sheikha G.A., Mubarak M.S. Anticancer Agents Med. Chem. 2018, 18, 263-276. doi 10.2174/1871520617666170911171152
- 14. Dodia N., Shah A. Indian J. Het. Chem. 1999, 9(2), 139-142.
- 15. Tedesco R., Shaw A.N., Bambal R., Chai D., Concha N.O., Darcy M.G., Dhanak D., Fitch D.M., Gates A., Gerhardt W.G., Halegoua D.L., Han C., Hofmann G.A., Johnston V.K., Kaura A.C., Liu N., Keenan R.M., Lin-Goerke J., Sarisky R.T., Wiggall K.J., Zimmerman M.N., Duffy K.J. J. Med. Chem. 2006, 49, 971-983. doi 10.1021/jm050855s
- 16. Furugohri T., Isobe K., Honda Y., Kamisato-Matsumoto C., Sugiyama N., Nagahara T., Morishima Y., Shibano T.J. Thromb. Haemostasis. 2008, 6, 1542-1549. doi 10.1111/j.1538-7836.2008.03064.x
- 17. Fjellström O., Akkaya S., Beisel H.G., Eriksson P.O., Erixon K., Gustafsson D., Jurva U., Kang D., Karis D., Knecht W., Nerme V., Nilsson I., Olsson T., Redzic A., Roth R., Sandmark J., Tigerstrom A., Oster L. PLoS One. 2015, 10, 1-42. doi 10.1371/journal.pone.0113705
- 18. Obaidullah A.J., Al-Horani R.A. Cardiovasc. Hematol. Agents Med. Chem. 2017, 15, 40-48. doi.10.2174/1871525715666170529093938
- 19. Amin K.M., Gawad N.M.A., Rahman D.E.A., El Ashry M.K.E. Bioorg. Chem. 2014, 52, 31-43. doi 10.1016/j.bioorg.2013.11.002
- 20. Verespy S., Mehta A.Y., Afosah, D., Al-Horani R.A., Desai U.R. Sci Rep. 2016, 6, 24043. doi 10.1038/srep24043
- 21. Riyadh S.M., Kheder N.A., Asiry A.M. Monatsh. Chem. 2013, 144, 1559-1567. doi 10.1007/s00706-013-1028-1
- 22. Abdelhamid A.O., Gomha S.M., El-Enany W.A.M.A. J. Heterocycl. Chem. 2019, 56, 426-432. doi 10.1002/jhet.3415
- 23. Уломский Е.Н., Деев У.Н., Шестакова Е.С., Русинов В.Л., Чупахин О.Н. Изв. АН, Сер. хим. 2002, 51, 1594-1600.
- 24. Ulomskii E.N., Deev S.L., Shestakova T.S.,Rusinov V.L., Chupakhin O.N. Russ. Chem. Bull. 2002, 51, 1737-1743. doi 10.1023/A:1021320025860
- 25. Abdelhamid A.O., Zohdy H.F., Zaida M.M. Ind. J. Chem. 2000, 39B, 202.
- 26. Crespan E., Alexandrova L., Khandazhinskaya A., Jasko M., Kukhanova M., Villani G., Hübscher U., Spadari S., Maga G. Nucleic Acids Res. 2007, 35, 45-57. doi 10.1093/nar/gkl1016
- 27. Русинов В.Л., Уломский Е.Н., Чупахин О.Н., Забаиров М.М., Кпапустин А.В., Митин А.В., Жураветский М.И., Виноград И.А. Хим.-фарм. ж. 1990, 24, 41-44.
- 28. Rusinov V.L., Ulomskii E.N., Chupakhin O.N., Zubairov M.M., Kapustin A.B., Mitin N.I., Zhiravetskii M.I., Vinograd I.A. Pharm. Chem. J. 1990, 24, 646-650. doi 10.1007/BF00767030
- 29. Русинов В.Л., Уломский Е.Н., Чупахин О.Н., Чарушин В.Н. Изв. АН, Сер. хим. 2008, 57, 967-996.
- 30. Rusinov V. L., Ulomskii E.N., Chupakhin O.N., Charushin V.N. Russ. Chem. Bull. 2008, 57, 985-1014. doi 10.1007/s11172-008-0130-8
- 31. Jashari A., Imeri F., Ballazhi L., Shabani A., Mikhova B., Drager G., Popovski E., Huwiler A. Bioorg. Med. Chem. 2014, 22, 2655-2661. doi 10.1016/j.bmc.2014.03.026
