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Mendeleev Communications, 2013, Volume 23, Issue 6, Pages 323–325
DOI: https://doi.org/10.1016/j.mencom.2013.11.006
(Mi mendc2701)
 

This article is cited in 17 scientific papers (total in 17 papers)

Communications

Synthesis and biological activity of a novel water-soluble methano[60]fullerene tetracarboxylic derivative

A. B. Korneva, A. S. Peregudovb, V. M. Martynenkoa, G. V. Gusevaa, T. E. Sashenkovaa, A. Yu. Rybkina, I. I. Faingolda, D. V. Mishchenkoa, R. A. Kotelnikovaa, N. P. Konovalovaa, J. Balzarinic, P. A. Troshina

a Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
c Rega Institute, Department of Microbiology and Immunology, Katholieke Universiteit Leuven, Leuven, Belgium
Abstract: A reaction of 3,3,4,4-tetrakis(methoxycarbonyl)benzophenone tosylhydrazone with fullerene C60 was used to obtain a novel methano-[60]fullerene derivative bearing four carboxylic groups, whose sodium and potassium salts are water-soluble. The compound possesses antiviral and anticancer activity as well as pronounced antioxidant properties in combination with a low toxicity.
Document Type: Article
Language: English


Citation: A. B. Kornev, A. S. Peregudov, V. M. Martynenko, G. V. Guseva, T. E. Sashenkova, A. Yu. Rybkin, I. I. Faingold, D. V. Mishchenko, R. A. Kotelnikova, N. P. Konovalova, J. Balzarini, P. A. Troshin, “Synthesis and biological activity of a novel water-soluble methano[60]fullerene tetracarboxylic derivative”, Mendeleev Commun., 23:6 (2013), 323–325
Linking options:
  • https://www.mathnet.ru/eng/mendc2701
  • https://www.mathnet.ru/eng/mendc/v23/i6/p323
  • This publication is cited in the following 17 articles:
    1. Jing Liu, Yong Qiang Dong, “Construction of turn-on mode fluorescent sensor for Pb<sup>2+</sup> and Al<sup>3+</sup> with structure of phthalic acid and tetraphenylethylene core”, Chin. Sci. Bull., 67:20 (2022), 2405  crossref
    2. Yuliya N Biglova, “[2 + 1] Cycloaddition reactions of fullerene C60 based on diazo compounds”, Beilstein J. Org. Chem., 17 (2021), 630  crossref
    3. A.Yu. Rybkin, A.Yu. Belik, N.S. Goryachev, P.A. Mikhaylov, O.A. Kraevaya, N.V. Filatova, I.I. Parkhomenko, A.S. Peregudov, A.A. Terent'ev, E.A. Larkina, A.F. Mironov, P.A. Troshin, A.I. Kotelnikov, “Self-assembling nanostructures of water-soluble fullerene[60]–chlorin e6 dyads: Synthesis, photophysical properties, and photodynamic activity”, Dyes and Pigments, 180 (2020), 108411  crossref
    4. Zuohu Chai, Liqiong Luo, Bo Jin, Yang Zhao, Lipengcheng Xiao, Guang Li, Ling Ding, Qingchun Zhang, Rufang Peng, “Fullerene Stabilizer 4,11,15,30-Tetraarylamino Fullerenoarylaziridine: Regioselective Synthesis, Crystallographic Characterization Derivatives, and Potential Application as Propellant Stabilizer”, ACS Appl. Energy Mater., 3:3 (2020), 3005  crossref
    5. Chui-Wei Wong, Alexander V. Zhilenkov, Olga A. Kraevaya, Denis V. Mischenko, Pavel A. Troshin, Shan-hui Hsu, “Toward Understanding the Antitumor Effects of Water-Soluble Fullerene Derivatives on Lung Cancer Cells: Apoptosis or Autophagy Pathways?”, J. Med. Chem., 62:15 (2019), 7111  crossref
    6. A.Yu Rybkin, A.Yu Belik, O.A. Kraevaya, E.A. Khakina, A.V. Zhilenkov, N.S. Goryachev, D. Volyniuk, J.V. Grazulevicius, P.A. Troshin, A.I. Kotelnikov, “Covalently linked water-soluble fullerene–fluorescein dyads as highly efficient photosensitizers: Synthesis, photophysical properties and photochemical action”, Dyes and Pigments, 160 (2019), 457  crossref
    7. Daniela Iannazzo, Alessandro Pistone, Stefania Ferro, Laura De Luca, Anna Maria Monforte, Roberto Romeo, Maria Rosa Buemi, Christophe Pannecouque, “Graphene Quantum Dots Based Systems As HIV Inhibitors”, Bioconjugate Chem., 29:9 (2018), 3084  crossref
    8. L. N. Islamova, V. P. Gubskaya, G. M. Fazleeva, T. A. Zhelonkina, Sh. K. Latypov, D. R. Sharafutdinova, I. A. Nuretdinov, O. G. Sinyashin, “Synthesis of derivatives of fullerenes C60 and C70 containing pharmacophore groups”, Mendeleev Commun., 27:2 (2017), 204–206  mathnet  crossref
    9. Ivan V. Mikheev, Liliya O. Usoltseva, Dmitry A. Ivshukov, Dmitry S. Volkov, Mikhail V. Korobov, Mikhail A. Proskurnin, “Approach to the Assessment of Size-Dependent Thermal Properties of Disperse Solutions: Time-Resolved Photothermal Lensing of Aqueous Pristine Fullerenes C60 and C70”, J. Phys. Chem. C, 120:49 (2016), 28270  crossref
    10. H. Liang, K. Dai, Zh. C. Guo, R. Peng, “C60(C6H4Me)4Ph4: a fully substituted derivative of the pentagon-fused C60Cl8”, Mendeleev Commun., 26:1 (2016), 29–31  mathnet  crossref
    11. Vincenzo Campisciano, Valeria La Parola, Leonarda F. Liotta, Francesco Giacalone, Michelangelo Gruttadauria, “Fullerene–Ionic‐Liquid Conjugates: A New Class of Hybrid Materials with Unprecedented Properties”, Chemistry A European J, 21:8 (2015), 3327  crossref
    12. Daniela Iannazzo, Alessandro Pistone, Signorino Galvagno, Stefania Ferro, Laura De Luca, Anna Maria Monforte, Tatiana Da Ros, Caroline Hadad, Maurizio Prato, Christophe Pannecouque, “Synthesis and anti-HIV activity of carboxylated and drug-conjugated multi-walled carbon nanotubes”, Carbon, 82 (2015), 548  crossref
    13. Danijela Petrovic, Mariana Seke, Branislava Srdjenovic, Aleksandar Djordjevic, Subhrajit Saha, “Applications of Anti/Prooxidant Fullerenes in Nanomedicine along with Fullerenes Influence on the Immune System”, Journal of Nanomaterials, 2015:1 (2015)  crossref
    14. O. L. Kobzar, V. V. Trush, V. Yu. Tanchuk, I. I. Voronov, A. S. Peregudov, P. A. Troshin, A. I. Vovk, “Polycarboxylic fullerene derivatives as protein tyrosine phosphatase inhibitors”, Mendeleev Commun., 25:3 (2015), 199–201  mathnet  crossref
    15. Q. Zhang, B. Jin, R. Peng, Sh. Lei, Sh. Chu, “Synthesis and characterization of a potential bifunctional C60-Ih fullerene-based catechol amide ligand”, Mendeleev Commun., 25:3 (2015), 204–206  mathnet  crossref
    16. S. V. Kurmaz, N. A. Obraztsova, “New hybrid nanostructures of C60 fullerene based on an amphiphilic copolymer of N-vinylpyrrolidone and (di)methacrylates”, Mendeleev Commun., 25:5 (2015), 350–352  mathnet  crossref
    17. A. R. Tuktarov, L. M. Khalilov, K. K. Babievskii, A. R. Akhmetov, V. I. Sokolov, U. M. Dzhemilev, “Circular dichroism spectra of new optically active terpenoid spiro homofullerenes”, Mendeleev Commun., 25:4 (2015), 273–274  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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