Мақаланы E-mail арқылы жіберу Application of the ANRORC-Process for the Directional Synthesis of 5-Ureido-2-Pyrazolines as a Biologically Active Co-Ligand of Gold Glyconanoparticles
- Авторлар: Ershov A.Y.1, Martynenkov A.A.1, Lagoda I.V.2, Batyrenko A.A.2
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Мекемелер:
- Institute of Macromolecular Compounds of the Russian Academy of Sciences
- State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation
- Шығарылым: Том 60, № 10 (2024)
- Беттер: 1078-1081
- Бөлім: КРАТКОЕ СООБЩЕНИЕ
- URL: https://aspvestnik.ru/0514-7492/article/view/682494
- DOI: https://doi.org/10.31857/S0514749224100112
- EDN: https://elibrary.ru/QKYXDQ
- ID: 682494
Дәйексөз келтіру
Ашық рұқсат
Рұқсат берілді
Аннотация
Interaction of 1-phenyl-4,6-dimethylpyrimidine-2(1H)-one with 4-mercaptobuturic acid hydrazide proceeds as ANRORC (Addition of the Nucleophile–Ring Opening–Ring Closure) process and gives in the formation with 60% yield of 1-(4-mercaptobutanoyl)-3,5-dimethyl-5-(3-phenylcarbamoylamino)-2-pyrazoline as promising сo-ligand for the preparation of gold glyconanoparticles for biomedical purposes.
Негізгі сөздер
Толық мәтін
Авторлар туралы
A. Ershov
Institute of Macromolecular Compounds of the Russian Academy of Sciences
Email: martynenkoff@gmail.com
ORCID iD: 0000-0002-2266-4380
Ресей, Bol′shoi prosp., 31, St. Petersburg, 199004
A. Martynenkov
Institute of Macromolecular Compounds of the Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: martynenkoff@gmail.com
ORCID iD: 0000-0002-0951-1451
Ресей, Bol′shoi prosp., 31, St. Petersburg, 199004
I. Lagoda
State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation
Email: martynenkoff@gmail.com
ORCID iD: 0000-0002-3906-2909
Ресей, Lesoparkovaya ul., 4, St. Petersburg, 195043
A. Batyrenko
State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation
Email: martynenkoff@gmail.com
ORCID iD: 0000-0001-9688-3650
Ресей, Lesoparkovaya ul., 4, St. Petersburg, 195043
Әдебиет тізімі
- Glycochemical synthesis: strategies and applications. Ed. S.-C. Hung, M. M. L. Zulueta. Hoboken, New Jersey: John Wiley & Sons Inc. 2016. doi: 10.1002/978 1119006435.ch16
- Mu W., Chu Q., Liu Y., Zhang N. Nano-Micro Lett. 2020, 12, е142. doi: 10.1007/s40820-020-00482-6
- Boije af Gennäs G., Mologni L., Ahmed S., Rajaratnam M., Marin O., Lindholm N., Viltadi M., Gambacorti-Passerini C., Scapozza L., Yli-Kauha-luoma J. Chem. Med. Chem. 2011, 6, 1680–1692. doi: 10.1002/cmdc.2011 00168
- Matiadis D., Sagnou M. Int. J. Mol. Sci. 2020, 21, e5507. doi: 10.3390/ijms21155507
- 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
- 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
- Ershov A.Y., Koshmina N.V. Arkivoc, 2000, vi, 917–922. doi: 10.3998/ark.5550190.0001.609
- Ершов А.Ю., Гиндин В.А., Грибанов А.В. ЖОрХ. 1997, 33, 438–441. [Ershov A.Y., Gindin V.V., Gribanov A.V. Russ. J. Org. Chem. 1997, 33, 388–391]. https:// www.pleiades. online/abstract/orgchem/97/orgchem0388_abstract.pdf
- van der Plas H.C. Adv. Heterocycl. Chem., 1999, 74, 87–151. doi: 10.1016/S0065-2725(08)60810-7
- Цаплин Г.В., Попков С.В. ЖOрХ. 2022, 58, 6–22. [Tsaplin G.V., Popkov S.V. Russ. J. Org. Chem. 2022, 58, 1–14.] doi: 10.1134/S1070428022010018
- Kashima C., Katoh A., Yokota Y., Omote Y. Chem. Pharm. Bull. 1981, 29, 2516–2519.
- doi: 10.1248/cpb.29.2516
- von Delius M., Geertsema E.M., Leigh D.A. Nat. Chem. 2010, 2, 96–101. doi 10.1038/ nchem.481.
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