New Heterocyclic Hepatitis C Virus (HCV) Inhibitors Containing A 2-Aminomethyl-1H-Indole Fragment von Ivachtchenko, A. V., Yamanushkin, P. M., Mit’kin, O. D., Ezhova, E. V., Korzinov, O. M., Bulanova, E. A., Bichko, V. V., Ivashchenko, A. A.

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Synthesis and Antiviral Activity of Ethyl 1,2-dimethyl-5-Hydroxy-1H-Indole-3-carboxylates and Their Derivatives von Ivashchenko, A. V., Yamanushkin, P. M., Mit’kin, O. D., Kisil’, V. M., Korzinov, O. M., Vedenskii, V. Yu, Leneva, I. A., Bulanova, E. A., Bychko, V. V., Okun’, I. M.

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Synthesis and Antiviral Activity of Substituted 2,4-bis-aminomethyl-5-hydroxy-1H-indole-3-carboxylic Acid Ethyl Esters and their Derivatives von Ivashchenko, A. V., Yamanushkin, P. M., Mit’kin, O. D., Kisil’, V. M., Korzinov, O. M., Vedenskii, V. Yu, Leneva, I. A., Bulanova, E. A., Bychko, V. V., Okun’, I. M., Ivashchenko, A. A., Ivanenkov, Ya. A.

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Synthesis and Antiviral Activity of Substituted Ethyl-2-Aminomethyl-5-Hydroxy-1H-Indole-3-Carboxylic Acids and Their Derivatives von Ivachtchenko, A. V., Yamanushkin, P. M., Mitkin, O. D., Kisil, V. M., Korzinov, O. M., Vedenskii, V. Yu, Leneva, I. A., Bulanova, E. A., Bichko, V. V., Okun’, I. M., Ivashchenko, A. A., Ivanenkov, Ya. A.

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Synthesis and radioligand activity of hydrogenated azepino[4,3-b]indoles von Mit’kin, O. D., Ivachtchenko, A. V., Frolov, E. B., Tkachenko, S. E., Kazey, V. I., Okun’, I. M.

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Antagonists of Serotonin 5-HT6 Receptors. VI. Substituted 3-(Phenylsulfonyl)Quinolines, Synthesis and Structure–Activity Relationships von Ivachtchenko, A. V., Golovina, E. S., Kadieva, M. G., Mitkin, O. D., Okun, I. M.

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Synthesis and antiviral activity of functionally substituted indole-3-acetic acids von Ivashchenko, A. V., Yamanushkin, P. M., Mit’kin, O. D., Leneva, I. A., Fedyakina, I. T.

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The synthesis and physiological activity of 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles von Ivashchenko, A V, Mitkin, O D, Kadieva, M G, Tkachenko, S E

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Syntheses and radioligand activities of dimebon analogs von Ivashchenko, A. V., Mit’kin, O. D., Okun’, I. M., Kuznetsova, I. V.

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Synthesis of hydrogenated 2,7-dimethylpyrrolo[3,4-b]indoles - analogs of dimebon von Ivachtchenko, A. V, Frolov, E. B, Mitkin, O. D, Tkachenko, S. E, Khvat, A. V

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Dithiane- and Trithiane-Based Photolabile Scaffolds for Molecular Recognition von Mitkin, Oleg D, Kurchan, Alexei N, Wan, Yongqin, Schiwal, Brian F, Kutateladze, Andrei G

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Novel oral anti-influenza prodrug candidate AV5075S von Ivachtchenko, Alexandre V, Ivanenkov, Yan A, Mitkin, Oleg D, Yamanushkin, Pavel M, Bichko, Vadim V, Shevkun, Natalia A, Mokrushina, Olga V, Nevolina, Olga O, Karapetian, Ruben N, Leneva, Irina A, Fedyakina, Irina T, Veselov, Mark S

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Synthesis of Dithiane-Based Photolabile Molecular Systems von Mitkin, Oleg D., Wan, Yongqin, Kurchan, Alexei N., Kutateladze, Andrei G.

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Antagonists of serotonin 5-HT6 receptors. III. Pyridine-substituted 3-(phenylsulfonyl)pyrazolo[1,5-a]pyrimidines: synthesis and structure – activity relationship von Ivashchenko, A. V., Golovina, E. S., Kadieva, M. G., Kysil, V. M., Mitkin, O. D., Okun, I. M.

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Quaternization of electron-deficient pyridines containing two electron-withdrawing substituents von Mit'kin, O. D., Yurovskaya, M. A.

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Functionalization of pyridines. 3. Reactions forming a carbon-heteroatom bond with group IV, V, and VI elements von Yurovskaya, M. A., Mit'kin, O. D.

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Homolytic ethoxycarbonylation of 3-nitropyridines von Yurovskaya, M. A., Mit'kin, O. D.

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Functionalization of pyridines. 2. Synthesis of acylpyridines, pyridinecarboxylic acids, and their derivatives. Review von Yurovskaya, M. A., Mit'kin, O. D., Zaitseva, F. V.

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5-Ht6 Receptor Antagonists. V. Structure – Activity Relationship of (4-Phenylsulfonyloxazol-5-yl)amines von Ivachtchenko, A. V., Golovina, E. S., Kadieva, M. G., Mitkin, O. D., Okun, I. M.

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Antagonists of serotonin 5-HT6 receptors. iv. synthesis and structure-activity interactions in amines containing the 3-(arylsulfonyl)-2-(methylthio)pyrazolo[1,5-a]pyrimidine fragme... von Ivachtchenko, A. V., Golovina, E. S., Kadieva, M. G., Kysil’, V. M., Mitkin, O. D.

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