Interaction of 5-Hydroxypyrazolidine with Thiol-Containing Hydrazides as a Method of Synthesis of Biologically Active Ligands of Gold Glyco-Nanoparticles

Cover Page

Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

The interaction of (3S)-1-acetyl-5-hydroxy-2-phenyl-3-methylpyrazolidine with 6-mercaptohexanoic and 11-mercaptoundecanoic acid hydrazides leads to the formation in 60–65% yields of (3S)-1-acetyl-5-[(ω-mercaptoacyl)hydrazine]-2-phenyl-3-methylpyrazolidines as a promising сo-ligands for the production of gold glyco-nanoparticles for biomedical purposes.

About the authors

A. Y. Ershov

Institute of Macromolecular Compounds of the Russian Academy of Sciences

Email: martynenkoff@gmail.com
ORCID iD: 0000-0002-2266-4380
Russian Federation, Bol′shoi prosp., 31, St. Petersburg, 199004

A. A. Martynenkov

Institute of Macromolecular Compounds of the Russian Academy of Sciences

Author for correspondence.
Email: martynenkoff@gmail.com
ORCID iD: 0000-0002-0951-1451
Russian Federation, Bol′shoi prosp., 31, St. Petersburg, 199004

I. V. 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
Russian Federation, Lesoparkovaya ul., 4, St. Petersburg, 195043

A. 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
Russian Federation, Lesoparkovaya ul., 4, St. Petersburg, 195043

References

  1. Kutterer K.M.K., Davis J.M., Singh G., Yang Y., Hu W., Severin A., Rasmussen B.A., Krishnamurthy G., Failli A., Katz A.H. Bioorg. Med. Chem. Lett. 2005, 15, 2527–2531. doi: 10.1016/j.bmcl.2005.03.058
  2. Moydeen M., Kumar R.S., Idhayadhulla A., Manilal A. Mol. Divers. 2019, 23, 35–53. doi: 10.1007/s11030-018-9850-3
  3. Cheon H.G., Kim S.-S., Kim K.-R., Rhee S.-D., Yang S.D., Ahn J.H., Park S.-D., Lee J.M., Jung W.H., Lee H.S., Kim H.Y. Biochem. Pharm. 2005, 70, 22–29. doi: 10.1016/j.bcp.2005.04.004
  4. 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
  5. Wang W., Wang J., Ding Y. J. Mat. Chem. (B). 2020, 8, 4813–4830. doi: 10.1039/c9tb02924a
  6. Glycochemical synthesis: strategies and applications. Eds. S.-C. Hung, M.M.L. Zulueta. Hoboken, New Jersey: John Wiley & Sons Inc. 2016. doi: 10.1002/978 1119006435.ch16
  7. 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, 1735–1739]. doi: 10.1134/S1070363221090 188
  8. Ершов А.Ю., Мартыненков А.А., Лагода И.В., Батыренко А.А., Драчев И.С., Якунчикова Е.А., Федорос Е.И., Круглов С.С., Копаница М.А., Якиманский А.В. ЖОХ. 2022, 92, 788–798. [Ershov A.Y., Martynenkov A.A., Lagoda I.V., Batyrenko A.A., Drachev I.S., Yakunchikova E.A., Fedoros E.I., Kruglov S.S., Kopanitsa M.A. Yakimansky A.V. Russ. J. Gen. Chem. 2022, 92, 850–859]. doi: 10.31857/S0044460X22050146
  9. Зеленин К.Н., Довгилевич А.В., Бежан И.П., Голубева Г.А., Свиридова Л.А., Пастушенков Л.В., Громова Е.Г., Гатчина Т.А., Помогайбо С.В. ХГС. 1984, 5, 659–666. [Zelenin K.N., Dovgilevich A.V., Bezhan I.P., Golubeva G.A., Sviridova L.A., Pastushenkov L.V., Gromova E.G., Gatchina T.A., Pomogaibo S.V. Chem. Heterocycl. Compd. 1984, 5, 529–536]. doi 10.1007/ BF00514307

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2025 Russian Academy of Sciences