Synthesis of Phosphoisosteres of Amyloid Dipeptide Components
- Авторлар: Golovash S.R.1, Ivanov D.E.1, Borodachev A.V.1, Shestov V.I.1, Dmitriev M.E.1, Ragulin V.V.1
 - 
							Мекемелер: 
							
- Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences
 
 - Шығарылым: Том 94, № 1 (2024)
 - Беттер: 98-104
 - Бөлім: Articles
 - URL: https://clinpractice.ru/0044-460X/article/view/667244
 - DOI: https://doi.org/10.31857/S0044460X24010081
 - EDN: https://elibrary.ru/HKVRCB
 - ID: 667244
 
Дәйексөз келтіру
Аннотация
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.
Толық мәтін
Авторлар туралы
S. Golovash
Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences
														Email: rvalery@dio.ru
				                					                																			                												                	Ресей, 							Chernogolovka						
D. Ivanov
Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences
														Email: rvalery@dio.ru
				                					                																			                												                	Ресей, 							Chernogolovka						
A. Borodachev
Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences
														Email: rvalery@dio.ru
				                	ORCID iD: 0000-0002-3458-5129
				                																			                												                	Ресей, 							Chernogolovka						
V. Shestov
Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences
														Email: rvalery@dio.ru
				                					                																			                												                	Ресей, 							Chernogolovka						
M. Dmitriev
Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences
														Email: rvalery@dio.ru
				                	ORCID iD: 0000-0001-8870-195X
				                																			                												                	Ресей, 							Chernogolovka						
V. Ragulin
Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry of the Russian Academy of Sciences
							Хат алмасуға жауапты Автор.
							Email: rvalery@dio.ru
				                	ORCID iD: 0000-0002-3967-1034
				                																			                												                	Ресей, 							Chernogolovka						
Әдебиет тізімі
- Collinsova M., Jiracek J. // Curr. Med. Chem. 2000. Vol. 7. N 6. P. 629. doi: 10.2174/0929867003374831
 - 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
 - Mucha A. // Molecules. 2012. Vol. 17. P. 13530. doi: 10.3390/molecules171113530
 - Georgiadis D., Dive V. // Top. Curr. Chem. 2015. Vol. 360. P. 1. doi: 10.1007/128_2014_571
 - Zinc Metalloproteases in Health and Disease // Ed. N.M. Hooper. London: Taylor and Francis, 1996. P. 153.
 - Hori M., Nishida K. // Cardiovasc. Res. 2009. Vol. 81. N 3. P. 457. doi: 10.1093/cvr/cvn335
 - Whittaker M., Ayscough A. // Celltransmissions. 2001. Vol. 17. N 1. P. 3.
 - Pirad B., Matter H. // J. Med. Chem. 2006. Vol. 49. N 1. P. 51. doi: 10.1021/jm050363f
 - Dafnis I., Argyri L., Chroni A. // Neuroscience. 2018. Vol. 394. P. 144. doi: 10.1016/j.neuroscience.2018.10.026
 - Sun X., Chen W.-D., Wang Y.-D. // Front. Pharmacol. 2015. Vol. 6. P. 1. doi: 10.3389/fphar.2015.00221
 - 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
 - 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
 - Musiek E.S., Holtzman D.M. // Neuroscience. 2015. Vol. 18. P. 800. doi: 10.1038/nn.4018
 - 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
 - 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
 - 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
 - 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
 - Rozhko L.F., Ragulin V.V. // Amino Acids. 2005. Vol. 29. P.139. doi: 10.1007/s00726-005-0194-9
 - Dmitriev M.E., Ragulin V.V. // Tetrahedron Lett. 2010. Vol. 51. N 19. P. 2613. doi: 10.1016/j.tetlet.2010.03.020
 - Dmitriev M.E., Ragulin V.V. // Tetrahedron Lett. 2012. Vol. 53. N 13. P. 1634. doi: 10.1016/j.tetlet.2012.01.094
 
Қосымша файлдар
				
			
						
					
						
						
						



