This article is cited in 3 scientific papers (total in 3 papers)
Communications
(E)-3-Arylidene-4-diazopyrrolidine-2,5-diones conveniently elaborated into cytotoxic compounds bearing primary sulfonamide and Michael acceptor moieties
Abstract:
The earlier described (E)-3-arylidene-4-diazopyrrolidine-2,5-diones have been elaborated into two distinct series of compounds both bearing a primary sulfonamide moiety and an electrophilic ‘Michael acceptor’ motif. These compounds demonstrated cytotoxicity against colorectal cancer cell line HCT 116.
Citation:
P. Paramonova, T. Sharonova, S. A. Kalinin, E. G. Chupakhin, A. S. Bunev, M. Yu. Krasavin, “(E)-3-Arylidene-4-diazopyrrolidine-2,5-diones conveniently elaborated into cytotoxic compounds bearing primary sulfonamide and Michael acceptor moieties”, Mendeleev Commun., 32:2 (2022), 176–177
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https://www.mathnet.ru/eng/mendc604
https://www.mathnet.ru/eng/mendc/v32/i2/p176
This publication is cited in the following 3 articles:
A. A. Panov, “Quantum Chemical Study of the Energies of Isomeric Maleimide and Itaconimide Derivatives”, Russ. J. Phys. Chem., 99:3 (2025), 522
V. Krivovicheva, A. Bubyrev, S. A. Kalinin, D. V. Dar'in, M. Gureev, D. Vullo, M. Yu. Krasavin, M. K. Korsakov, C. T. Supuran, “A new way of synthesizing heterocyclic primary sulfonamide probes for carbonic anhydrase”, Mendeleev Commun., 33:3 (2023), 325–327
A. Yu. Lukin, L. V. Vinogradova, K. Yu. Komarova, S. A. Kalinin, M. Yu. Krasavin, “Synthesis of 1-oxa-9-azaspiro[5.5]undecane-9-sulfonamides bearing a diverse molecular periphery and a rare zinc-binding group for carbonic anhydrase interrogation”, Mendeleev Commun., 33:2 (2023), 191–193
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