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Mendeleev Communications, 2023, Volume 33, Issue 4, Pages 550–552
DOI: https://doi.org/10.1016/j.mencom.2023.06.035
(Mi mendc456)
 

This article is cited in 4 scientific papers (total in 4 papers)

Communications

Microwave-assisted synthesis of 5-aryl-3-hydroxy-2-oxindole derivatives and evaluation of their antiglaucomic activity

A. M. Efremovab, D. A. Babkovc, O. V. Beznosd, E. V. Sokolovac, A. A. Spasovc, V. N. Ivanovb, A. V. Kurkinb, N. B. Chesnokovad, N. A. Lozinskayab

a Institute of Physiologically Active Compounds, Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
b Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
c Volgograd State Medical University, Volgograd, Russian Federation
d Helmholtz National Medical Centre of Eye Diseases, Moscow, Russian Federation
Full-text PDF (312 kB) Citations (4)
Abstract: A set of new 5-aryl-3-hydroxy-2-oxindoles was synthesized by decarboxylative condensation of the corresponding 5-aryl-substituted isatins with malonic or cyanoacetic acids under microwave irradiation. The antiglaucomic activity of the obtained compounds was evaluated. The most water soluble compounds can reduce the intraocular pressure (IOP) up to 2 Torr.
Keywords: oxindole, indolin-2-one, NRH:quinone oxidoreductase 2 inhibitors, intraocular pressure, antiglaucomic, microwave irradiation, condensation.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (808.1 Kb)


Citation: A. M. Efremov, D. A. Babkov, O. V. Beznos, E. V. Sokolova, A. A. Spasov, V. N. Ivanov, A. V. Kurkin, N. B. Chesnokova, N. A. Lozinskaya, “Microwave-assisted synthesis of 5-aryl-3-hydroxy-2-oxindole derivatives and evaluation of their antiglaucomic activity”, Mendeleev Commun., 33:4 (2023), 550–552
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  • https://www.mathnet.ru/eng/mendc456
  • https://www.mathnet.ru/eng/mendc/v33/i4/p550
  • This publication is cited in the following 4 articles:
    1. Alla K. Shestakova, Vladislav V. Stanishevskiy, Vyacheslav A. Chertkov, “The parameters of the multiplet structure of the NMR spectra of [15N]indole and their relationship with the molecular electronic structure”, Chem Heterocycl Comp, 2025  crossref
    2. Roman O. Eremeev, Alexander M. Efremov, Daria V. Zakharova, Olga V. Beznos, Elena V. Sokolova, Konstantin Y. Kalitin, Olga Y. Mukha, Daria V. Vinogradova, Ivan M. Veselov, Pavel N. Shevtsov, Ludmila G. Dubova, Denis A. Babkov, Alexander A. Spasov, Elena F. Shevtsova, Natalia A. Lozinskaya, “Discovery of Novel 2‐Oxindoles as Compounds with Antiglaucoma Activity”, ChemMedChem, 2025  crossref
    3. N. I. Vikrishchuk, O. P. Demidov, O. I. Askalepova, L. D. Popov, Yu. I. Ryabukhin, “Crystal structure and properties of new benzimidazopyrido[2,3-b]indole-6-carbonitriles”, Mendeleev Commun., 34:2 (2024), 274–276  mathnet  crossref
    4. Alla K. Shestakova, Vladislav V. Stanishevskiy, Vyacheslav A. Chertkov, “Synthesis and NMR spectra of [15N]indole”, Chem Heterocycl Comp, 59:9-10 (2023), 657  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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