A. Ivachtchenko

发表

Screening for Caspase-3 Inhibitors: A New Class of Potent Small-Molecule Inhibitors of Caspase-3

Alexey P. Ilyin, L. Sklar, E. Prossnitz, 2006, Journal of biomolecular screening.

Synthesis, inhibitory activity and oral dosing formulation of AV5124, the structural analogue of influenza virus endonuclease inhibitor baloxavir.

E. Govorkova, Jeremy C. Jones, V. Aladinskiy, 2020, The Journal of antimicrobial chemotherapy.

Synthesis and antimicrobial activity of 5-hydroxymethyl- 8-methyl-2-(N-arylimino)-pyrano[2,3-c]pyridine-3-(N-aryl)-carboxamides.

K. Balakin, A. Ivachtchenko, I. O. Zhuravel, 2005, Bioorganic & medicinal chemistry letters.

Multicomponent approach to unique 1,4-diazepine-2-amines

S. Tkachenko, A. Khvat, V. Kysil, 2009 .

Novel aryl and heteroaryl substituted N-[3-(4-phenylpiperazin-1-yl)propyl]-1,2,4-oxadiazole-5-carboxamides as selective GSK-3 inhibitors.

Y. Ivanenkov, I. Okun, R. Karapetian, 2008, Bioorganic & medicinal chemistry letters.

Aprotinin ‐ a new multi-target drug candidate or "magic shotgun" for the therapy of COVID‐19

S. Poyarkov, A. Ivashchenko, R. Karapetian, 2020 .

Small-molecule inhibitors of hepatitis C virus (HCV) non-structural protein 5A (NS5A): a patent review (2010-2015)

Y. Ivanenkov, V. Aladinskiy, A. Majouga, 2017, Expert opinion on therapeutic patents.

Safety and efficacy of aviandr in patients with generalized anxiety disorder: A multicenter, randomized, double-blind, placebo-controlled, dose-finding, pilot study.

O. Bukhanovskaya, A. Ivashchenko, R. Karapetian, 2021, Journal of psychiatric research.

From anti-allergic to anti-Alzheimer's: Molecular pharmacology of Dimebon.

S. Tkachenko, I. Okun, A. Khvat, 2010, Current Alzheimer research.

Caspase activity modulators as anticancer agents.

K. Balakin, S. Tkachenko, I. Okun, 2008, Anti-cancer agents in medicinal chemistry.

AVN-322 is a Safe Orally Bio-Available Potent and Highly Selective Antagonist of 5-HT6R with Demonstrated Ability to Improve Impaired Memory in Animal Models.

Y. Ivanenkov, M. Veselov, I. Okun, 2016, Current Alzheimer research.

Effect of Aprotinin and Avifavir® Combination Therapy for Moderate COVID-19 Patients

N. Savchuk, S. Poyarkov, A. Ivashchenko, 2021, Viruses.

A novel mesoionic ring system: unusual cyclization of thio- and amino-acid derivatives of 6-azauracil

A. Kiselyov, J. Hammaker, F. Lakner, 2005 .

5-Ht6 Receptor Antagonists. V. Structure – Activity Relationship of (4-Phenylsulfonyloxazol-5-yl)amines

I. Okun, M. Kadieva, A. Ivachtchenko, 2013, Pharmaceutical Chemistry Journal.

Antagonists of 5-HT₆ receptors. Substituted 3-(phenylsulfonyl)pyrazolo[1,5-a]pyrido[3,4-e]pyrimidines and 3-(phenylsulfonyl)pyrazolo[1,5-a]pyrido[4,3-d]pyrimidines-Synthesis and 'structure-activity' relationship.

I. Okun, M. Kadieva, V. Kysil, 2012, Bioorganic & medicinal chemistry letters.

A novel solid-phase synthesis of cyclic guanidines

A. Kiselyov, A. Ivachtchenko, V. Vvedensky, 2005 .

The Efficacy of Aprotinin Combinations with Selected Antiviral Drugs in Mouse Models of Influenza Pneumonia and Coronavirus Infection Caused by SARS-CoV-2

Y. Ivanenkov, B. Zagribelnyy, A. Ivashchenko, 2022, Molecules.

Aprotinin is a potent multi-target drug for the combination therapy of moderate COVID-19 cases

N. Savchuk, S. Poyarkov, A. Ivashchenko, 2020 .

Regioselective synthesis of substituted isoxazolo[5,4-d]pyrimidines

D. Kravchenko, A. Ivachtchenko, Sergey B. Alyabiev, 2008 .

Liquid-phase synthesis of combinatorial libraries based on 7-trifluoromethyl-substituted pyrazolo[1,5-a]pyrimidine scaffold.

S. Shevelev, I. Dalinger, I. A. Vatsadse, 2005, Journal of combinatorial chemistry.

AVIFAVIR for Treatment of Patients With Moderate Coronavirus Disease 2019 (COVID-19): Interim Results of a Phase II/III Multicenter Randomized Clinical Trial

N. Savchuk, A. Ivashchenko, R. Karapetian, 2020, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

One-step assembly of carbamoyl substituted annulated 1,4-oxazepines

Alexey P. Ilyin, S. Tkachenko, D. Kravchenko, 2006 .

One-step assembly of carbamoyl-substituted heteroannelated [1,4]thiazepines.

Alexey P. Ilyn, S. Tkachenko, M. Krasavin, 2006, The Journal of organic chemistry.

Synthesis and biological activity of 5-styryl and 5-phenethyl-substituted 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles.

I. Okun, E. Frolov, A. Ivachtchenko, 2010, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological evaluation of novel 5-oxo-2-thioxoimidazolidine derivatives as potent androgen receptor antagonists.

Y. Ivanenkov, M. Veselov, N. Shevkun, 2015, European journal of medicinal chemistry.

Complexity-enhancing acid-promoted rearrangement of tricyclic products of tandem Ugi 4CC/intramolecular Diels-Alder reaction.

Mikhail Krasavin, Volodymyr Kysil, Alexandre V Ivachtchenko, 2006, The Journal of organic chemistry.

General Multicomponent Strategy for the Synthesis of 2‐Amino‐1,4‐diazaheterocycles: Scope, Limitations, and Utility

S. Tkachenko, Caroline T Williams, A. Khvat, 2010 .

Poorly reactive 5-piperazin-1-yl-1,3,4-thiadiazol-2-amines rendered as valid substrates for Groebke–Blackburn type multi-component reaction with aldehydes and isocyanides using TMSCl as a promoter

Mikhail Nikulnikov, Mikhail Krasavin, Sergey Tsirulnikov, 2008 .

One-pot tandem complexity-generating reaction based on Ugi four component condensation and intramolecular cyclization

Alexey P. Ilyin, V. Kysil, A. Ivachtchenko, 2007 .

Multi-Component Reactions in Heterocyclic Chemistry

R. R. Khairullina, I. V. Paramonov, Alexey P. Ilyn, 2011 .

Streamlined access to 2,3-dihydropyrazino[1,2-a]indole-1,4-diones via Ugi reaction followed by microwave-assisted cyclization

M. Krasavin, V. Kysil, A. Ivachtchenko, 2009 .

AN EFFICIENT SYNTHESIS OF 3-OXO-1,2,3,4-TETRAHYDROPYRROLO[1,2-α]PYRAZINE-1-CARBOXAMIDES USING NOVEL MODIFICATION OF UGI CONDENSATION

Alexey P. Ilyn, Alexandre M. Shkirando, A. Ivachtchenko, 2005 .

One-step construction of peptidomimetic 5-carbamoyl-4-sulfonyl-2-piperazinones.

M. Krasavin, A. Ivachtchenko, A. S. Trifilenkov, 2005, Journal of combinatorial chemistry.

An efficient synthesis of novel 1,3-oxazolo[4,5-d]pyridazinones

F. Lakner, E. Frolov, A. Ivachtchenko, 2004 .

Synthesis and structure-activity relationship (SAR) of (5,7-disubstituted 3-phenylsulfonyl-pyrazolo[1,5-a]pyrimidin-2-yl)-methylamines as potent serotonin 5-HT(6) receptor (5-HT(6)R) antagonists.

S. Tkachenko, I. Okun, M. Kadieva, 2011, Journal of medicinal chemistry.

(3-Phenylsulfonylcycloalkano[e and d]pyrazolo[1,5-a]pyrimidin-2-yl)amines: potent and selective antagonists of the serotonin 5-HT6 receptor.

S. Tkachenko, I. Okun, M. Kadieva, 2010, Journal of medicinal chemistry.

TMSCl-promoted isocyanide-based MCR of ethylenediamines: an efficient assembling of 2-aminopyrazine core

S. Tkachenko, Caroline T Williams, A. Khvat, 2007 .

Natural products as templates for bioactive compound libraries: Part 2. Novel modifications of vasicine (peganine) core via efficient and regioselective generation of 3-lithiodeoxyvasicine and its stereoselective addition to aliphatic ketones

A. Kiselyov, M. Krasavin, O. I. Davydova, 2006, Natural product research.

Natural products as templates for bioactive compound libraries: synthesis of biaryl derivatives of (±)-vasicine

S. Tkachenko, A. Kiselyov, M. Krasavin, 2006, Natural product research.

New Scaffolds for Combinatorial Synthesis. II. 6-Sulfamoylquinolinecarboxylic Acids

Alexey P. Ilyin, A. Ivachtchenko, V. V. Kobak, 2003 .

Synthesis and biological study of 3-(phenylsulfonyl)thieno[2,3-e][1,2,3]triazolo[1,5-a]pyrimidines as potent and selective serotonin 5-HT6 receptor antagonists.

S. Tkachenko, I. Okun, M. Kadieva, 2010, Bioorganic & medicinal chemistry.

Synthesis of 7,8‐Dihydrothieno[3′,2′:4,5]pyrrolo[1,2‐a]pyrazin‐5(6H)‐ones Using a Modification of Four‐Component Ugi Reaction

Alexey P. Ilyin, S. Tkachenko, I. Dmitrieva, 2006 .

An efficient synthesis of novel heterocycle-fused derivatives of 1-oxo-1,2,3,4-tetrahydropyrazine using Ugi condensation

Alexey P. Ilyn, Alexandre M. Shkirando, S. Tkachenko, 2005 .

Synthesis of cycloalkane-annelated 3-phenylsulfonyl-pyrazolo[1,5-a]pyrimidines and their evaluation as 5-HT6 receptor antagonists.

S. Tkachenko, I. Okun, M. Kadieva, 2010, Bioorganic & medicinal chemistry letters.

Solution phase parallel synthesis of substituted 3-phenylsulfonyl-[1,2,3]triazolo[1,5-a]quinazolines: selective serotonin 5-HT(6) receptor antagonists.

S. Tkachenko, I. Okun, M. Kadieva, 2010, Journal of combinatorial chemistry.

Synthesis of substituted 4-oxo-2-thioxo-1,2,3,4-tetrahydroquinazolines and 4-oxo-3,4-dihydroquinazoline-2-thioles.

A. Ivachtchenko, S. Kovalenko, O. G. Drushlyak, 2003, Journal of combinatorial chemistry.

Sulfonyl-containing modulators of serotonin receptors and their pharmacophore models

A. Ivachtchenko, 2014 .

Design of Multi-Component Reactions

A. S. Medvedeva, Alexey P. Ilyin, V. A. Glushkov, 2011 .

New four-component Ugi-type reaction. Synthesis of heterocyclic structures containing a pyrrolo[1,2-a][1,4]diazepine fragment.

A. V. Nikitin, Alexey P. Ilyn, A. Ivachtchenko, 2005, The Journal of organic chemistry.

Streamlined Access to 2,3‐Dihydropyrazino[1,2‐a]indole‐1,4‐diones via Ugi Reaction Followed by Microwave‐Assisted Cyclization.

M. Krasavin, V. Kysil, A. Ivachtchenko, 2010 .

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

Y. Ivanenkov, V. Bichko, I. Okun, 2015, Pharmaceutical Chemistry Journal.

Liquid‐Phase Synthesis of Combinatorial Libraries Based on 7‐Trifluoromethyl‐Substituted Pyrazolo[1,5‐a]pyrimidine Scaffold.

S. Shevelev, I. Dalinger, I. A. Vatsadse, 2005 .

Synthesis and Structure−Activity Relationship of 4-Substituted 2-(2-Acetyloxyethyl)-8-(morpholine- 4-sulfonyl)pyrrolo[3,4-c]quinoline- 1,3-diones as Potent Caspase-3 Inhibitors

K. Balakin, S. Tkachenko, I. Okun, 2005 .

1,3-Dioxo-4-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]quinolines as potent caspase-3 inhibitors.

Alexey P. Ilyn, S. Tkachenko, I. Okun, 2005, Bioorganic & medicinal chemistry letters.

Synthesis of pinacol esters of 1-alkyl-1H-pyrazol-5-yl- and 1-alkyl-1H-pyrazol-4-ylboronic acids

A. Ivachtchenko, D. Kravchenko, D. G. Pershin, 2004 .

A convenient synthesis of heterocyclic compounds containing 11-oxo-6,11,12,13-tetrahydrodibenzo[b,g][1,5]oxazonine fragment

A. Ivachtchenko, V. V. Potapov, N. A. Fetisova, 2009 .

One-step assembly of novel carbamoyl substituted 6-oxo-4,5,6,11-tetrahydropyrrolo[1,2-b][2,5]benzodiazocine

A. V. Nikitin, A. Ivachtchenko, V. V. Potapov, 2009 .

A New Insight into the Pfitzinger Reaction. A Facile Synthesis of 6‐Sulfamoylquinoline‐4‐carboxylic Acids.

Caroline T Williams, A. Khvat, A. Ivachtchenko, 2004 .

Synthesis of the Substituted 3‐Cyclobutene‐1,2‐diones

A. Ivachtchenko, D. Kravchenko, S. Ivanovsky, 2007 .

Synthesis and Biological Evaluation of Novel 5,8‐Disubstituted‐2‐methyl‐2,3,4,5‐tetrahydro‐1H‐pyrido[4,3‐b] indoles as 5‐HT6 and H1 Receptors Antagonists

S. Tkachenko, E. Frolov, A. Khvat, 2009, Archiv der Pharmazie.

Methylation of Methyl 4-Hydroxy-2-thioxo-1,2-dihydroquinoline-3-carboxylate: Synthetic, Crystallographic, and Molecular Docking Studies

T. Langer, V. Ivanov, S. Shishkina, 2020, Molecules.

Pyrrolo[3,4-c]Quinoline-1,3-Diones as Potent Caspase-3 Inhibitors: Synthesis and SAR of 8-Sulfamoyl-1,3-Dioxo-2,3-Dihydro-1H-Pyrrolo[3,4- c]Quinolines

S. Tkachenko, I. Okun, D. Kravchenko, 2006 .

Pyrrolo[3,4-c]quinoline-1,3-diones as potent caspase-3 inhibitors. Synthesis and SAR of 2-substituted 4-methyl-8-(morpholine-4-sulfonyl)-pyrrolo[3,4-c]quinoline-1,3-diones.

S. Tkachenko, I. Okun, D. Kravchenko, 2005, European journal of medicinal chemistry.

Screening for Caspase-3 Inhibitors: Effect of a Reducing Agent on Identified Hit Chemotypes

S. Tkachenko, I. Okun, S. Malarchuk, 2006, Journal of biomolecular screening.

Synthesis and caspase-3 inhibitory activity of 8-sulfonyl-1,3-dioxo-2,3-dihydro-1H-pyrrolo[3,4-c]quinolines.

S. Tkachenko, I. Okun, D. Kravchenko, 2005, Farmaco.

1,3‐Dioxo‐4‐methyl‐2,3‐dihydro‐1H‐pyrrolo[3,4‐c]quinolines as Potent Caspase‐3 Inhibitors.

Alexey P. Ilyn, S. Tkachenko, I. Okun, 2005 .

AVIFAVIR for Treatment of Patients with Moderate COVID-19: Interim Results of a Phase II/III Multicenter Randomized Clinical Trial

A. Ivashchenko, R. Karapetian, I. Gordeev, 2020 .

Interim Results of a Phase II/III Multicenter Randomized Clinical Trial of AVIFAVIR in Hospitalized Patients with COVID-19

N. Savchuk, A. Ivashchenko, R. Karapetian, 2020, medRxiv.

Synthesis of heterocyclic compounds possessing the 4H-thieno[3,2-b]pyrrole moiety.

Alexey P. Ilyin, I. Dmitrieva, A. Ivachtchenko, 2007, Journal of combinatorial chemistry.

Synthesis of substituted 3‐(5‐amino‐[1,3,4]thiadiazol‐2‐yl)‐2H‐pyrano[2,3‐c]pyridin‐2‐ones

A. Ivachtchenko, I. O. Zhuravel, S. Kovalenko, 2004 .

Crystal structure, Hirshfeld analysis and a molecular docking study of a new inhibitor of the Hepatitis B virus (HBV): ethyl 5-methyl-1,1-dioxo-2-{[5-(pentan-3-yl)-1,2,4-oxadiazol-3-yl]methyl}-2H-1,2,6-thiadiazine-4-carboxylate

T. Langer, V. Ivanov, A. Ivachtchenko, 2020, Acta crystallographica. Section E, Crystallographic communications.

Small-molecule modulators of Hh and Wnt signaling pathways

K. Balakin, S. Tkachenko, A. Kiselyov, 2007, Expert opinion on therapeutic targets.

Cyclic products of the Ugi reaction of aldehydo and keto carboxylic acids: chemoselective modification

S. Tkachenko, M. Krasavin, A. Ivachtchenko, 2011 .

A Comprehensive Insight into the Chemical Space and ADME Features of Small Molecule NS5A Inhibitors.

Anastasia V Aladinskaya, V. Koteliansky, S. Leonov, 2016, Current topics in medicinal chemistry.

Recent progress in discovery and development of antimitotic agents.

K. Balakin, N. Savchuk, S. Tkachenko, 2007, Anti-cancer agents in medicinal chemistry.

AVN-101: A Multi-Target Drug Candidate for the Treatment of CNS Disorders

I. Okun, Y. Lavrovsky, A. Ivachtchenko, 2016, Journal of Alzheimer's disease : JAD.

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

V. Bichko, P. Yamanushkin, A. Ivachtchenko, 2015, Pharmaceutical Chemistry Journal.

AVN-211, Novel and Highly Selective 5-HT6 Receptor Small Molecule Antagonist, for the Treatment of Alzheimer's Disease.

Y. Ivanenkov, Y. Lavrovsky, A. Ivachtchenko, 2016, Molecular pharmaceutics.

Synthesis and SAR of 3-arylsulfonyl-pyrazolo[1,5-a]pyrimidines as potent serotonin 5-HT6 receptor antagonists.

S. Tkachenko, I. Okun, M. Kadieva, 2011, Bioorganic & medicinal chemistry.

5-hydroxytryptamine subtype 6 receptor modulators: a patent survey

Yan A Ivanenkov, Y. Ivanenkov, S. Tkachenko, 2010, Expert opinion on therapeutic patents.

5HT6 receptor antagonists: a patent update. Part 1. Sulfonyl derivatives

Y. Ivanenkov, A. Ivachtchenko, 2012, Expert opinion on therapeutic patents.

Synthesis and biological evaluation of novel gamma-carboline analogues of Dimebon as potent 5-HT6 receptor antagonists.

S. Tkachenko, I. Okun, E. Frolov, 2009, Bioorganic & medicinal chemistry letters.

Synthesis and caspase-3 inhibitory activity of 8-sulfonyl-1,3-dioxo-2,3-dihydro-1H-pyrrolo[3,4-c]quinolines.

S. Tkachenko, I. Okun, D. Kravchenko, 2005, Farmaco.

Discovery of novel highly potent hepatitis C virus NS5A inhibitor (AV4025).

Y. Ivanenkov, M. Veselov, V. Bichko, 2014, Journal of medicinal chemistry.

Non-dopamine receptor ligands for the treatment of Parkinson’s disease. Insight into the related chemical/property space

Y. Ivanenkov, M. Veselov, A. Majouga, 2016, Molecular Diversity.

Add-on clinical effects of selective antagonist of 5HT6 receptors AVN-211 (CD-008-0173) in patients with schizophrenia stabilized on antipsychotic treatment: pilot study

M. Morozova, Y. Lavrovsky, A. Ivachtchenko, 2013, CNS Spectrums.

AVN-492, A Novel Highly Selective 5-HT6R Antagonist: Preclinical Evaluation.

Y. Ivanenkov, V. Aladinskiy, I. Okun, 2017, Journal of Alzheimer's disease : JAD.

Novel oral anti-influenza drug candidate AV5080.

Y. Ivanenkov, M. Veselov, V. Bichko, 2014, The Journal of antimicrobial chemotherapy.

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

I. Okun, M. Kadieva, A. Ivachtchenko, 2015, Pharmaceutical Chemistry Journal.

Synthesis of 5H-Pyrazolo[4,3-c]quinolines

A. Ivachtchenko, S. Kovalenko, T. I. Savchenko, 2004 .

Synthesis, Single Crystal X-Ray Analysis, Prediction and Study of Pharmacological Activity of 4-(1H-Benzo[d]imidazol-2-yl)-1-Phenyl-1H-1,2,3-triazol-5-Amine and Its Solvates

T. Langer, V. Ivanov, S. Shishkina, 2019, Crystals.

8-Sulfonyl-substituted tetrahydro-1H-pyrido[4,3-b]indoles as 5-HT6 receptor antagonists.

S. Tkachenko, I. Okun, V. Kysil, 2010, European journal of medicinal chemistry.

Bromination of indomethacin

O. Kiselev, P. Yamanushkin, A. Ivachtchenko, 2010 .

Liquid-phase parallel synthesis of combinatorial libraries of substituted 6-carbamoyl-3,4-dihydro-2H-benzo[1,4]thiazines.

S. Tkachenko, A. Khvat, A. Ivachtchenko, 2006, Journal of combinatorial chemistry.

Synthesis of 7-arylimidazo[1,2-a]pyrazin-8(7H)-one derivatives

S. S. Kovalenko, A. Ivachtchenko, D. Kravchenko, 2019, Chemistry of Heterocyclic Compounds.

Access to novel substituted diazaadamantanes via semi-natural tetrahydrocytisine

S. Tkachenko, A. Ivachtchenko, V. Vvedensky, 2004 .

Synthesis and receptor activity of 2-substituted 8-methyl-5-(2-pyridinylethyl)-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles

I. Okun, V. Kysil, A. Ivachtchenko, 2013, Pharmaceutical Chemistry Journal.

Novel oral anti-influenza prodrug candidate AV5075S.

Y. Ivanenkov, M. Veselov, V. Bichko, 2014, Journal of Antimicrobial Chemotherapy.

A novel influenza virus neuraminidase inhibitor AV5027.

Y. Ivanenkov, V. Bichko, O. Borisova, 2013, Antiviral research.

Synthesis, X-ray crystal structure, Hirshfeld surface analysis, and molecular docking study of novel inhibitor of hepatitis B: methyl 4-fluoro-3-(morpholinosulfonyl)benzo[b]thiophene-2-carboxylate

T. Langer, V. Ivanov, S. Shishkina, 2019, Heliyon.

Aprotinin—Drug against Respiratory Diseases

A. Ivashchenko, A. Ivachtchenko, I. A. Ivashchenko, 2023, International journal of molecular sciences.

Non-rigid Diarylmethyl Analogs of Baloxavir as CAP-Dependent Endonuclease Inhibitors of Influenza Viruses.

E. Govorkova, Jeremy C. Jones, V. Aladinskiy, 2020, Journal of medicinal chemistry.

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

Y. Ivanenkov, V. Bichko, I. Okun, 2015, Pharmaceutical Chemistry Journal.

SYNTHESIS OF BENZIMIDAZO[1,2-c]QUINAZOLINE-6(5H)-THIONES

A. Ivachtchenko, S. Kovalenko, O. G. Drushlyak, 2002 .

Microwave-mediated reactions of 3-aminomethylpyridines with acetylenedicarboxylates. A novel synthetic route to dihydronaphthyridines and naphthyridine-1-ones

A. Kiselyov, Y. Ivanov, Caroline T Williams, 2005 .

Microwave‐Mediated Reactions of 3‐Aminomethylpyridines with Acetylenedicarboxylates. A Novel Synthetic Route to Dihydronaphthyridines and Naphthyridine‐1‐ones.

A. Kiselyov, Y. Ivanov, Caroline T Williams, 2005 .

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

S. Tkachenko, E. Frolov, A. Ivachtchenko, 2010 .

Synthesis of Annelated Azaheterocycles Containing a 5-Carbamoylpyrazin-3-one Fragment by a Modification of the Four-Component Ugi Reaction

S. Tkachenko, I. Dmitrieva, A. Ivachtchenko, 2005 .

AVN-211, Novel and Highly Selective 5-HT6 Receptor Small Molecule Antagonist, for the Treatment of Alzheimer's Disease.

Y. Ivanenkov, Y. Lavrovsky, A. Ivachtchenko, 2016, Molecular Pharmaceutics.

2-Substituted 5,6-dimethyl-3-phenylsulfonyl-pyrazolo[1,5-a]pyrimidines: new series of highly potent and specific serotonin 5-HT6 receptor antagonists.

S. Tkachenko, I. Okun, M. Kadieva, 2011, European journal of medicinal chemistry.

CXCR4 receptor as a promising target for oncolytic drugs.

K. Balakin, Y. Ivanenkov, Y. Lavrovsky, 2008, Mini reviews in medicinal chemistry.

Preclinical Development of ONC1-13B, Novel Antiandrogen for Prostate Cancer Treatment

N. Shevkun, R. Karapetian, A. Ivachtchenko, 2014, Journal of Cancer.

Synthesis of substituted diphenyl sulfones and their structure-activity relationship with the antagonism of 5-НТ6 receptors.

I. Okun, M. Kadieva, A. Ivachtchenko, 2013, Bioorganic & medicinal chemistry.

Antiviral susceptibility of clade 2.3.4.4b highly pathogenic avian influenza A(H5N1) viruses isolated from birds and mammals in the United States, 2022

Ha T. Nguyen, C. Davis, L. Gubareva, 2023, Antiviral research.