RAS Chemistry & Material ScienceЖурнал общей химии Russian Journal of General Chemistry

  • ISSN (Print) 0044-460X
  • ISSN (Online) 3034-5596

Synthesis of Phosphoisosteres of Amyloid Dipeptide Components

PII
10.31857/S0044460X24010081-1
DOI
10.31857/S0044460X24010081
Publication type
Article
Status
Published
Authors
Volume/ Edition
Volume 94 / Issue number 1
Pages
98-104
Abstract
A simple and effective method was proposed for the synthesis of new phosphinic peptides in free form, structural isosteres of the dipeptide components of beta-amyloid (Aβ42), potential inhibitors of zinc-metalloproteinases.
Keywords
карбаматная версия реакции Кабачника–Филдса амилоид ацетилхлорид уксусный ангидрид амидоалкилирование фосфиновые кислые пептиды
Date of publication
16.09.2025
Year of publication
2025
Number of purchasers
0
Views
12

References

  1. 1. Collinsova M., Jiracek J. // Curr. Med. Chem. 2000. Vol. 7. N 6. P. 629. doi 10.2174/0929867003374831
  2. 2. Dive V., Georgiadis D., Matziari M., Makaritis A., Beau F., Cuniasse P., Yiotakis A. // Cell. Mol. Life Sci. 2004. Vol. 61. P. 2010. doi 10.1007/s00018-004-4050-y
  3. 3. Mucha A. // Molecules. 2012. Vol. 17. P. 13530. doi 10.3390/molecules171113530
  4. 4. Georgiadis D., Dive V. // Top. Curr. Chem. 2015. Vol. 360. P. 1. doi 10.1007/128_2014_571
  5. 5. Zinc Metalloproteases in Health and Disease // Ed. N.M. Hooper. London: Taylor and Francis, 1996. P. 153.
  6. 6. Hori M., Nishida K. // Cardiovasc. Res. 2009. Vol. 81. N 3. P. 457. doi 10.1093/cvr/cvn335
  7. 7. Whittaker M., Ayscough A. // Celltransmissions. 2001. Vol. 17. N 1. P. 3.
  8. 8. Pirad B., Matter H. // J. Med. Chem. 2006. Vol. 49. N 1. P. 51. doi 10.1021/jm050363f
  9. 9. Dafnis I., Argyri L., Chroni A. // Neuroscience. 2018. Vol. 394. P. 144. doi 10.1016/j.neuroscience.2018.10.026
  10. 10. Sun X., Chen W.-D., Wang Y.-D. // Front. Pharmacol. 2015. Vol. 6. P. 1. doi 10.3389/fphar.2015.00221
  11. 11. Xiong Z.M., Kitagawa K., Nishiuchi Y., Kimura T., Nakamura T., Inagaki C. // Life Sci. 2009. Vol. 84. P. 132. doi 10.1016/j.lfs.2008.11.011
  12. 12. Xiong Z.M., Kitagawa K., Nishiuchi Y., Kimura T., Inagaki C. // Neurosci. Lett. 2007. Vol. 419. N 3. P. 247. doi 10.1016/j.neulet.2007.04.022
  13. 13. Musiek E.S., Holtzman D.M. // Neuroscience. 2015. Vol. 18. P. 800. doi 10.1038/nn.4018
  14. 14. Dafnis I., Argyri L., Sagnou M., Tzinia A., Tsilibary E.C., Stratikos E., Chroni A. // Sci Rep. 2016. Vol. 6. P. 30654. doi 10.1038/srep30654
  15. 15. Argyri L., Dafnis I., Theodossiou T.A., Gantz D., Stratikos E., Chroni A. // J. Biol. Chem. 2014. Vol. 289. P.12931. doi 10.1074/jbc.M113.538124
  16. 16. Дмитриев М.Э., Рагулин В.В. // ЖОХ. 2015. Т. 85. Вып. 9. С. 1511; Dmitriev M.E., Ragulin V.V. // Russ. J. Gen. Chem. 2015. Vol. 85. N 9. P. 2091. doi 10.1134/S1070363215090121
  17. 17. Dmitriev M.E., Golovash S.R., Borodachev A.V., Ragulin V.V. // J. Org. Chem. 2021. Vol. 86. N 1. P.593. doi 10.1021/acs.joc.0c02259
  18. 18. Rozhko L.F., Ragulin V.V. // Amino Acids. 2005. Vol. 29. P.139. doi 10.1007/s00726-005-0194-9
  19. 19. Dmitriev M.E., Ragulin V.V. // Tetrahedron Lett. 2010. Vol. 51. N 19. P. 2613. doi 10.1016/j.tetlet.2010.03.020
  20. 20. Dmitriev M.E., Ragulin V.V. // Tetrahedron Lett. 2012. Vol. 53. N 13. P. 1634. doi 10.1016/j.tetlet.2012.01.094
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