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New Heterocyclic Hepatitis C Virus (HCV) Inhibitors Containing A 2-Aminomethyl-1H-Indole Fragment

Pharmaceutical chemistry journal, 2015-09, Vol.49 (6), p.352-361

2015

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Synthesis and Antiviral Activity of Ethyl 1,2-dimethyl-5-Hydroxy-1H-Indole-3-carboxylates and Their Derivatives

Pharmaceutical chemistry journal, 2014-03, Vol.47 (12), p.636-650

2014

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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

Pharmaceutical chemistry journal, 2014-12, Vol.48 (9), p.569-581

2014

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Preclinical study of AV0012 early stage inhibitor of hepatitis C virus infection: I. In vitro ADME and pharmacokinetics

Ėksperimentalʹnaâ i kliničeskaâ farmacologiâ, 2014, Vol.77 (4), p.33

2014

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Synthesis and Antiviral Activity of Substituted Ethyl-2-Aminomethyl-5-Hydroxy-1H-Indole-3-Carboxylic Acids and Their Derivatives

Pharmaceutical chemistry journal, 2015-06, Vol.49 (3), p.151-162

2015

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Synthesis and radioligand activity of hydrogenated azepino[4,3-b]indoles

Pharmaceutical chemistry journal, 2012-05, Vol.46 (2), p.103-113

2012

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Antagonists of Serotonin 5-HT6 Receptors. VI. Substituted 3-(Phenylsulfonyl)Quinolines, Synthesis and Structure–Activity Relationships

Pharmaceutical chemistry journal, 2015-01, Vol.48 (10), p.646-660

2015

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Synthesis and antiviral activity of functionally substituted indole-3-acetic acids

Pharmaceutical chemistry journal, 2011-08, Vol.45 (5), p.261, Article 261

2011

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The synthesis and physiological activity of 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles

Russian chemical reviews, 2010-01, Vol.79, p.285

2010

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Syntheses and radioligand activities of dimebon analogs

Pharmaceutical chemistry journal, 2011-12, Vol.45 (9), p.526-531

2011

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Synthesis of hydrogenated 2,7-dimethylpyrrolo[3,4-b]indoles - analogs of dimebon

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2010-06, Vol.46 (2), p.170-178

2010

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Preclinical study of the new anti-influenza drug candidate AV0038 (ethyl 2-(dimethylaminomethyl)-5-hydroxy-1-methyl-6-(pyridin-3-yl)-1H-indole-3-carboxylate)

Ėksperimentalʹnaâ i kliničeskaâ farmacologiâ, 2014, Vol.77 (5), p.23

2014

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Preclinical study of safety of the new pharmacological substance AV0012 to treat hepatitis C

Ėksperimentalʹnaâ i kliničeskaâ farmacologiâ, 2014, Vol.77 (12), p.33

2014

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Antiviral activity in vitro and pharmacokinetics of HCV entry inhibitor AVR560

Ėksperimentalʹnaâ i kliničeskaâ farmacologiâ, 2014, Vol.77 (10), p.38

2014

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Substituted 2,3,4,5-tetrahydro-1H-gamma-carbolines: new antagonists of histamine H1 receptors

Ėksperimentalʹnaâ i kliničeskaâ farmacologiâ, 2010-11, Vol.73 (11), p.25

2010

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Toxicity of ethyl-3-(8-fluoro-2-methyl-2,3,4,5-tetrahydropyrido[4,3-bindol-5-yl)-propionate dihydrochloride possessing antiallergic properties

Ėksperimentalʹnaâ i kliničeskaâ farmacologiâ, 2010-06, Vol.73 (6), p.33

2010

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Anti-allergic properties of a novel ethyl 3-(8-fluoro-2-methyl-2,3,4,5-tetrahydropyrido[4,3-bindol-5-yl)propionate dihydrochloride

Ėksperimentalʹnaâ i kliničeskaâ farmacologiâ, 2010-03, Vol.73 (3), p.28

2010

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Dithiane- and Trithiane-Based Photolabile Scaffolds for Molecular Recognition

Organic letters, 2001-06, Vol.3 (12), p.1841-1844

2001

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Novel oral anti-influenza prodrug candidate AV5075S

Journal of antimicrobial chemotherapy, 2014-05, Vol.69 (5), p.1311-1324

2014

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Synthesis of Dithiane-Based Photolabile Molecular Systems

Synthesis (Stuttgart), 2001-01, Vol.112 (8)

2001

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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

Pharmaceutical chemistry journal, 2012-10, Vol.46 (7), p.406-410

2012

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Quaternization of electron-deficient pyridines containing two electron-withdrawing substituents

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2000-01, Vol.36 (1), p.47-48

2000

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Functionalization of pyridines. 3. Reactions forming a carbon-heteroatom bond with group IV, V, and VI elements

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 1999-04, Vol.35 (4), p.383-435

1999

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Homolytic ethoxycarbonylation of 3-nitropyridines

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 1997-11, Vol.33 (11), p.1299-1300

1997

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Functionalization of pyridines. 2. Synthesis of acylpyridines, pyridinecarboxylic acids, and their derivatives. Review

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 1998-08, Vol.34 (8), p.871-899

1998

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New Heterocyclic Hepatitis C Virus (HCV) Inhibitors Containing A 2-Aminomethyl-1H-Indole Fragment

Synthesis and Antiviral Activity of Ethyl 1,2-dimethyl-5-Hydroxy-1H-Indole-3-carboxylates and Their Derivatives

Synthesis and Antiviral Activity of Substituted 2,4-bis-aminomethyl-5-hydroxy-1H-indole-3-carboxylic Acid Ethyl Esters and their Derivatives

Preclinical study of AV0012 early stage inhibitor of hepatitis C virus infection: I. In vitro ADME and pharmacokinetics

Synthesis and Antiviral Activity of Substituted Ethyl-2-Aminomethyl-5-Hydroxy-1H-Indole-3-Carboxylic Acids and Their Derivatives

Synthesis and radioligand activity of hydrogenated azepino[4,3-b]indoles

Antagonists of Serotonin 5-HT6 Receptors. VI. Substituted 3-(Phenylsulfonyl)Quinolines, Synthesis and Structure–Activity Relationships

Synthesis and antiviral activity of functionally substituted indole-3-acetic acids

The synthesis and physiological activity of 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles

Syntheses and radioligand activities of dimebon analogs

Synthesis of hydrogenated 2,7-dimethylpyrrolo[3,4-b]indoles - analogs of dimebon

Preclinical study of the new anti-influenza drug candidate AV0038 (ethyl 2-(dimethylaminomethyl)-5-hydroxy-1-methyl-6-(pyridin-3-yl)-1H-indole-3-carboxylate)

Preclinical study of safety of the new pharmacological substance AV0012 to treat hepatitis C

Antiviral activity in vitro and pharmacokinetics of HCV entry inhibitor AVR560

Substituted 2,3,4,5-tetrahydro-1H-gamma-carbolines: new antagonists of histamine H1 receptors

Toxicity of ethyl-3-(8-fluoro-2-methyl-2,3,4,5-tetrahydropyrido[4,3-bindol-5-yl)-propionate dihydrochloride possessing antiallergic properties

Anti-allergic properties of a novel ethyl 3-(8-fluoro-2-methyl-2,3,4,5-tetrahydropyrido[4,3-bindol-5-yl)propionate dihydrochloride

Dithiane- and Trithiane-Based Photolabile Scaffolds for Molecular Recognition

Novel oral anti-influenza prodrug candidate AV5075S

Synthesis of Dithiane-Based Photolabile Molecular Systems

Antagonists of serotonin 5-HT6 receptors. III. Pyridine-substituted 3-(phenylsulfonyl)pyrazolo[1,5-a]pyrimidines: synthesis and structure – activity relationship

Quaternization of electron-deficient pyridines containing two electron-withdrawing substituents

Functionalization of pyridines. 3. Reactions forming a carbon-heteroatom bond with group IV, V, and VI elements

Homolytic ethoxycarbonylation of 3-nitropyridines

Functionalization of pyridines. 2. Synthesis of acylpyridines, pyridinecarboxylic acids, and their derivatives. Review

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