Further validation of Strecker-type α-aminonitriles as a new class of potent human carbonic anhydrase II inhibitors: hit expansion within the public domain using differential scanning fluorimetry leads to chemotype refinement, J. Enzyme Inhib. Med. Chem., 2020, 35, 165-171, M.Krasavin, S.Kalinin, S.Zozulya, A.Gryniukova, P.Borysko, A.Angeli, C.T.Supuran Screening of benzenesulfonamide in combination with chemically diverse fragments against carbonic anhydrase by differential scanning fluorimetry, J. Enzyme Inhib. Med. Chem., 2020, 35, 306-310, M.Krasavin, S.Kalinin, S.Zozulya, A.Gryniukova, P.Borysko, A.Angeli, C.T.Supuran Highly Hydrophilic 1,3-Oxazol-5-yl Benzenesulfonamide Inhibitors of Carbonic Anhydrase II for Reduction of Glaucoma-Related Intraocular Pressure, Bioorganic and Medicinal Chemistry, 2019, 27, 115086, S.Kalinin, A.Valtari, A.Ruponen, E.Toropainen, A.Kovalenko, A.Nocentini, M.Gureev, D.Dar'in, A.Urtti, C.T.Supuran, M.Krasavin From random to rational: A Discovery Approach to Selective Subnanomolar Inhibitors of Human Carbonic Anhydrase IV Based on the Castagnoli-Cushman Multicomponent Reaction, European Journal of Medicinal Chemistry, 2019, 182, 111642, S.Kalinin, A.Nocentini, A.Kovalenko, V.Sharoyko, A.Bonardi, A.Angeli, P.Gratteri, T.B.Tennikova, C.T.Supuran, M.Krasavin Pyridazinone-substituted benzenesulfonamides display potent inhibition of membrane-bound human carbonic anhydrase IX and promising antiproliferative activity against cancer cell lines, European Journal of Medicinal Chemistry, 2019, 168, 301-314, M.Krasavin, A.Shetnev, S.Baykov, S.Kalinin, A.Nocentini, V.Sharoyko, G.Poli, T.Tuccinardi, M.Korsakov, T.B.Tennikova, C.T.Supuran 1,2,4-Oxadiazole/2-imidazoline hybrids: Multi-target-directed compounds for the treatment of infectious diseases and cancer, Int. 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Sci., 2019, 20, 1699, A.Shetnev, S.Baykov, S.Kalinin, A.Belova, V.Sharoyko, A.Rozhkov, L.Zelenkov, M.Tarasenko, E.Sadykov, M.Korsakov, M.Krasavin Continued exploration of 1,2,4-oxadiazole periphery for carbonic anhydrase-targeting primary arene sulfonamides: discovery of subnanomolar inhibitors of membrane-bound hCA IX isoform that selectively kill cancer cells in hypoxic environment, European Journal of Medicinal Chemistry, 2019, 164, 92-105, M.Krasavin, A.Shetnev, T.Sharonova, S.Baykov, S.Kalinin, A.Nocentini, V.Sharoyko, G.Poli, T.Tuccinardi, S.Presnukhina, T.B.Tennikova, C.T.Supuran Unprotected primary sulfonamide group facilitates ring-forming cascade en route to polycyclic [1.4]oxazepine-based carbonic anhydrase inhibitors, Bioorganic Chemistry, 2018, 76, 140-146, A.Sapegin, S.Kalinin, A.Angeli, C.T.Supuran, M.Krasavin Heterocyclic Periphery in the Design of Carbonic Anhydrase Inhibitors: 1,2,4-Oxadiazol-5-yl Benzenesulfonamides as Potent and Selective Inhibitors of Cytosolic hCA II and Membrane-Bound hCA IX Isoforms, Bioorganic Chemistry, 2018, 76, 88-97, M.Krasavin, A.Shetnev, T.Sharonova, S.Baykov, T.Tuccinardi, S.Kalinin, A.Angeli, C.T.Supuran The first one-pot ambient-temperature synthesis of 1,2,4-oxadiazoles from amidoximes and carboxylic acid esters, Tetrahedron, 2017, 73, 945-951, S.Baykov, T.Sharonova, A.Shetnev, S.Rozhkov, S.Kalinin, A.V.Smirnov Primary mono- and bis-sulfonamides obtained via regiospecific sulfochlorination of N-arylpyrazoles: inhibition profile against a panel of human carbonic anhydrases, Journal of Enzyme Inhibition and Medicinal Chemistry, 2017, 32, 920-934, M.Krasavin, M.Korsakov, O.Ronzhina, T.Tuccinardi, S.Kalinin, M.Tanç, C.T.Supuran Human carbonic anhydrase inhibitory profile of mono- and bis-sulfonamides synthesized via a direct sulfochlorination of 3-and 4-(hetero)arylisoxazol-5-amine scaffolds, Bioorganic and Medicinal Chemistry, 2017, 25, 1914-1925, M.Krasavin, M.Korsakov, Z.Zvonaryova, E.Semyonychev, T.Tuccinardi, S.Kalinin, M.Tanç, C.T.Supuran Synthesis, structure and properties of N-aminosaccharin - A selective inhibitor of human carbonic anhydrase I, Tetrahedron Letters, 2017, 58, 172-174, M.A.Kuznetsov, A.N.Shestakov, M.Zibinsky, M.Krasavin, C.T.Supuran, S.Kalinin, M.Tanç Lucky Switcheroo: Dramatic Potency and Selectivity Improvement of Imidazoline Inhibitors of Human Carbonic Anhydrase VII, ACS Medicinal Chemistry Letters, 2017, 8, 1105-1109, S.Kalinin, S.Kopylov, T.Tuccinardi, A.Sapegin, D.Dar'in, A.Angeli, C.T.Supuran, M.Krasavin Isoform-selective inhibitory profile of 2-imidazoline-substituted benzenesulfonamides against a panel of human carbonic anhydrases, Journal of Enzyme Inhibition and Medicinal Chemistry, 2016, 31, 197-202, C.T.Supuran, S.Kalinin, M.Tanç, P.Sarnpitak, P.Mujumdar, S.-A.Poulsen, M.Krasavin Multicomponent chemistry in the synthesis of carbonic anhydrase inhibitors, Journal of Enzyme Inhibition and Medicinal Chemistry, 2016, 31, 185-199, S.Kalinin, C.T.Supuran, M.Krasavin Efficient Use of 1,2-Dihaloazine Synthons in Transition Metal-Free Preparation of Diverse Heterocycle-Fused 1,4-Oxazepines, Eur. J. Org. Chem., 2015, 1333-1340, A.Sapegin, S.Kalinin, A.Smirnov, M.Dorogov, M.Krasavin New tetracyclic 1,4-oxazepines constructed via practically simple tandem condensation strategy from readily available synthons, Tetrahedron, 2014, 70, 1077-1083, A.Sapegin, S.Kalinin, A.Smirnov, M.Dorogov, M.Krasavin Dibenzo[b,f]pyrazolo[1,5-d][1,4]oxazepines: a facile construction of a rare heterocyclic system via tandem aromatic nucleophilic substitution - Smiles rearrangement – denitrocyclization, Synthesis, 2012, 44, 2401-2407, A.Sapegin, S.Kalinin, A.Smirnov, M.Dorogov, M.Krasavin