Application of the Knorr reaction for the directional synthesis of pyrazole derivative as a biologically active co-ligandes of gold glyco-nanoparticles
- Авторлар: Ershov A.Y.1, Martynenkov A.A.1, Lagoda I.V.2, Batyrenko A.A.2
- 
							Мекемелер: 
							- Institute of Macromolecular Compounds of Russian Academy of Sciences
- State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation
 
- Шығарылым: Том 59, № 11 (2023)
- Беттер: 1489-1491
- Бөлім: Articles
- URL: https://rjeid.com/0514-7492/article/view/667142
- DOI: https://doi.org/10.31857/S0514749223110101
- EDN: https://elibrary.ru/NCKVEC
- ID: 667142
Дәйексөз келтіру
Аннотация
Based on the reaction of acetylacetone with 6-mercaptohexanoic and 11-mercaptoundecanoic acid hydrazides, a method was developed for the synthesis of previously unknown 1-(ω-mercaptoacyl)-3,5-dimethylpyrazole as promising сo-ligand for the preparation of gold glyco-nanoparticles for biomedical purposes.
			                Негізгі сөздер
Авторлар туралы
A. Ershov
Institute of Macromolecular Compounds of Russian Academy of Sciences
														Email: ershov305@mail.ru
				                					                																			                												                														
A. Martynenkov
Institute of Macromolecular Compounds of Russian Academy of Sciences
I. Lagoda
State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation
A. Batyrenko
State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation
Әдебиет тізімі
- Ling L.E., Lee W.-C. Curr. Pharm. Biotech. 2011, 12, 2190-2202. doi: 10.2174/138920111798808257
- Rostami H., Shiri L., Khani Z. Tetrahedron. 2022, 110, 132688. doi: 10.1016/j.tet.2022.132688
- Федянин М.Ю., Хмелькова Д.Н., Серебрийская Т.С., Никольская Т.А., Тюляндин С.А. Усп. Молекул. Онкол. 2015, 2, 027-038.
- Fedyanin M.Yu., Khmelkova D.N., Serebriyskaya T.S., Nikolskaya T.A., Tyulyandin S.A. Adv. Mol. Oncol. 2015, 2, 027-032. doi: 10.17650/2313-805X.2015.2.1.027-038
- Banday A.H., Saeed B.A., Al-Masoudi N.A. Anti-Canсer Agen. Med. Chem. 2021, 21, 1671-1679. doi: 10.2174/1871520620999201124213655
- Naim M.J., Alam O., Nawaz F., Alam J., Alam P. J. Pharm. Bioallied Sci. 2016, 8, 2-17. doi: 10.4103/0975-7406.171694
- Adak A.K., Yu C.-C., Lin C.-C. Glycochemical Synthesis: Strategies and Applications. Eds. S.-C. Hung, M.M.L. Zulueta. Hoboken: John Wiley & Sons Inc. 2016. doi: 10.1002/9781119006435.ch16
- Knorr L. Ber. 1883, 16, 2597-2599. doi: 10.1002/cber.188301602194.
- Jazayeri M.H., Amani H., Pourfatollah A.A., Avan A., Ferns G.A., Pazoki-Toroudi H. Cancer Gene Ther. 2016, 23, 365-369. doi: 10.1038/cgt.2016.42
- Ершов А.Ю., Мартыненков А.А., Лагода И.В., Копаница М.А., Зарубаев В.В., Слита А.В., Бучков Е.В., Панарин Е.Ф., Якиманский А.В. ЖОХ. 2021, 91, 1459-1464.
- Ershov A.Y., Martynenkov A.A., Lagoda I.V., Kopanitsa M.A., Zarubaev V.V., Slita A.V., Buchkov E.V., Panarin E.F., Yakimansky A.V. Russ. J. Gen. Chem. 2021, 91, 1459-1464. doi: 10.1134/S1070363221090188
- Ershov A.Y., Martynenkov A.A., Lagoda I.V., Kopanitsa M.A., Yakimansky A.V. ChemestrySelect. 2019, 44, 12938-12941. doi: 10.1002/slct.201902942
Қосымша файлдар
 
				
			 
						 
					 
						 
						 
						

 
  
  
  Мақаланы E-mail арқылы жіберу
			Мақаланы E-mail арқылы жіберу 
 Ашық рұқсат
		                                Ашық рұқсат Рұқсат берілді
						Рұқсат берілді Рұқсат ақылы немесе тек жазылушылар үшін
		                                							Рұқсат ақылы немесе тек жазылушылар үшін
		                                					