Synthesis and effect of substituted pyrido[2,3-d]pyrimidine-2,4-diones on In Vitro tumor dna methylation

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 订阅存取

详细

Reaction of 3-diethylamino-1-aryl-, 3-diethylamino-1-aryl-2-phenyl(4-halophenyl)propane-1-ones hydrochlorides with 6-amino-1,3-dimethyluracil results in heterocyclization products, namely 1,3-dimethyl-7-aryl-5,6dihydro-1 H -pyrido[2,3- d ]pyrimidine-2,4-diones, 1,3-dimethyl-7-aryl-6-phenyl(4-halophenyl)-5,6-dihydro1 H -pyrido[2,3- d ]pyrimidine-2,4-diones and 1,3-dimethyl-7-aryl-6-phenyl-(4-halophenyl)-1 H -pyrido[2,3- d ] pyrimidine-2,4-diones. The effect of the synthesized compounds in vitro tumor DNA methylation was studied.

作者简介

A. Isakhanyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia

Email: anush.isakhanyan.51@mail.ru

N. Hakobyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia

Z. Hovasyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia

L. Nersesyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia

A. Aharonyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia

I. Danielyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia

H. Panosyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia

A. Harutyunyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia

参考

  1. Мещерякова С.А. Дисс. … докт. фарм. наук. Уфа, 2015.
  2. Fares M., Abou-Seri S.M., Abdel-Aziz H.A., Abbas S.E., Youssef M.M., Eladwy R.A. // Eur. J. Med. Chem. 2014. Vol. 83. P. 155. doi: 10.1016/j.ejmech.2014.06.027
  3. Abadi A.H., Hany M.S., Elsharif S.A., Eissa A.A., Gary B.D., Tinsley H.N., Piazza G.A. // Chem. Pharm. Bull. 2013. Vol. 61. N 4. P. 405. doi: 10.1248/cpb.c12-00993
  4. Vanyushin B.F. // JSM Genet. Genomics. 2016. Vol. 3. N 1. P. 1010.
  5. Azad N., Zahnow C.A., Rudin C.M., Baylin S.B. // Nat. Rev. Clin. Oncol. 2013. Vol. 10. N 5. P 256. doi: 10.1038/nrclinonc.2013.42
  6. Геворгян Г.А., Авакян А.П., Агабабян А.Г., Акопян Н.З., Маркарян Т.А., Паносян Г.А. // Хим. ж. Армении. 2013. T. 66. № 4. С. 597.
  7. Baylin S.B., Herman J.G. // Trends Genetics. 2000. Vol. 16. N 4. P. 168.
  8. Howell P.M., Jr., Liu Z., Khong H.T. // Pharmaceuticals. 2010. Vol. 3. N 7. P. 2022. doi: 10.3390/ph3072022
  9. Геворгян Г.А., Авакян А.П., Гаспарян Н.К., Паносян Г.А. // ЖОрХ. 2009. Т. 45. С. 1854
  10. Gevorgyan G.A., Avakyan A.P., Gasparyan N.K., Panosyan G.A. // Russ. J. Org. Chem. 2009. Vol. 45. P. 1853. doi: 10.1134/S1070428009120173
  11. Vanyushin B.F., Masin A.L., Vasiliev V.K., Belozersky A.N. // Biochim. Biophys. Acta. 1973. Vol. 299. N 3. P. 397. doi: 10.1016/0005-2787(73)90264-5

补充文件

附件文件
动作
1. JATS XML

版权所有 © Russian Academy of Sciences, 2023