A. Shchekotikhin

发表

Characterization of HERG potassium channel inhibition using CoMSiA 3D QSAR and homology modeling approaches.

Roy J. Vaz, M. Preobrazhenskaya, R. Pearlstein, 2003, Bioorganic & medicinal chemistry letters.

Heterocyclic analogs of 5,12-naphtacenequinone 13*. Synthesis of 4,11-diaminoanthra[2,3-b]furan-5,10-diones and sulfur-containing analogs

A. Shchekotikhin, A. Korolev, A. Tikhomirov, 2016, Chemistry of Heterocyclic Compounds.

Synthesis, biological evaluation, and in silico studies of potential activators of apoptosis and carbonic anhydrase inhibitors on isatin-5-sulfonamide scaffold.

C. Supuran, D. Vullo, V. De Luca, 2021, European journal of medicinal chemistry.

Synthesis of 7-amino-6-halogeno-3-phenylquinoxaline-2-carbonitrile 1,4-dioxides: a way forward for targeting hypoxia and drug resistance of cancer cells

A. Shchekotikhin, A. Scherbakov, L. Dezhenkova, 2021, RSC advances.

Antibiotic heliomycin and its water-soluble 4-aminomethylated derivative provoke cell death in T24 bladder cancer cells by targeting sirtuin 1 (SIRT1).

P. Chueh, A. Shchekotikhin, Chia-Wei Weng, 2022, American journal of cancer research.

Aminomethylation of heliomycin: Preparation and anticancer characterization of the first series of semi-synthetic derivatives.

Y. Yang, P. Chueh, D. Schols, 2018, European journal of medicinal chemistry.

Revision of the Regioselectivity of the Beirut Reaction of Monosubstituted Benzofuroxans with Benzoylacetonitrile. 6-Substituted quinoxaline-2-carbonitrile 1,4- dioxides: Structural Characterization and Estimation of Anticancer Activity and Hypoxia Selectivity.

P. Dorovatovskii, A. Shchekotikhin, A. Scherbakov, 2020, Current organic synthesis.

Discovery of derivatives of 6(7)-amino-3-phenylquinoxaline-2-carbonitrile 1,4-dioxides: novel, hypoxia-selective HIF-1α inhibitors with strong antiestrogenic potency.

S. Solovieva, A. Shchekotikhin, D. Sorokin, 2020, Bioorganic chemistry.

Naphthoindoles. 9. Synthesis of N-derivatives of 4,11-Dimethoxynaphtho-[2,3-f]indole-5,10-dione

A. Shchekotikhin, K. F. Turchin, N. N. Suvorov, 2000 .

Heterocyclic ring expansion yields anthraquinone derivatives potent against multidrug resistant tumor cells.

D. Andreeva, A. Shtil, V. Tsvetkov, 2022, Bioorganic chemistry.

Discovery of dihydrofuranoallocolchicinoids - Highly potent antimitotic agents with low acute toxicity.

P. Barbier, Diane Allegro, B. Gigant, 2020, European journal of medicinal chemistry.

Synthesis and evaluation of new antitumor 3-aminomethyl-4,11-dihydroxynaphtho[2,3-f]indole-5,10-diones.

Y. Pommier, M. Preobrazhenskaya, J. Balzarini, 2014, European journal of medicinal chemistry.

A functional study of the global transcriptional regulator PadR from a strain Streptomyces fradiae‐nitR+bld, resistant to nitrone‐oligomycin

V. Danilenko, A. Shchekotikhin, L. N. Lysenkova, 2018, Journal of basic microbiology.

Development and pharmaceutical evaluation of the anticancer Anthrafuran/Cavitron complex, a prototypic parenteral drug formulation

A. Shchekotikhin, A. Tikhomirov, A. Nikitin, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Photosensitization of pancreatic cancer cells by cationic alkyl-porphyrins in free form or engrafted into POPC liposomes: The relationship between delivery mode and mechanism of cell death.

Francesca D'Este, A. Shchekotikhin, S. Vogel, 2022, Journal of photochemistry and photobiology. B, Biology.

Sequencing and analysis of the resistome of Streptomyces fradiae ATCC19609 in order to develop a test system for screening of new antimicrobial agents

V. Danilenko, A. Shchekotikhin, A. Korolev, 2016, Russian Journal of Genetics.

Pd-catalyzed cross-coupling/heterocyclization domino reaction: facile access to anthra[2,3- b ]furan-5,10-dione scaffold

M. Preobrazhenskaya, A. Shchekotikhin, A. Korolev, 2014 .

The first series of 4,11-bis[(2-aminoethyl)amino]anthra[2,3-b]furan-5,10-diones: Synthesis and anti-proliferative characteristics.

M. Preobrazhenskaya, J. Balzarini, A. Shtil, 2011, European journal of medicinal chemistry.

Synthesis and cytotoxic properties of 4,11-bis[(aminoethyl)amino]anthra[2,3-b]thiophene-5,10-diones, novel analogues of antitumor anthracene-9,10-diones.

M. Preobrazhenskaya, J. Balzarini, A. Shtil, 2009, Bioorganic & medicinal chemistry.

Antitumor Anthraquinone Analogues for Multidrug Resistant Tumor Cells

M. Preobrazhenskaya, A. Shtil, Hsu-Shan Huang, 2006 .

Potent Apoptotic Response Induced by Chloroacetamidine Anthrathiophenediones in Bladder Cancer Cells.

A. Shchekotikhin, S. Zorzet, S. Cogoi, 2015, Journal of medicinal chemistry.

Computational and Biophysical Characterization of Heterocyclic Derivatives of Anthraquinone against Human Aurora Kinase A

P. Kaur, A. Shchekotikhin, A. Tikhomirov, 2022, ACS omega.

Discovery Of Amphamide, A Drug-Candidate For The Second Generation Of Polyene Antibiotics.

S. Solovieva, A. Shchekotikhin, E. Mirchink, 2020, ACS infectious diseases.

Pharmacological Assessment of the Carvacrol Chemotype Essential Oil From Plectranthus amboinicus Growing in Cuba

W. Setzer, L. Gille, A. Shchekotikhin, 2020 .

Synthesis and Characterization of 4,11-Diaminoanthra[2,3-b]furan-5,10-diones: Tumor Cell Apoptosis through tNOX-Modulated NAD(+)/NADH Ratio and SIRT1.

M. Preobrazhenskaya, Yi-Hui Lee, P. Chueh, 2015, Journal of medicinal chemistry.

Essential Oil from Melaleuca leucadendra: Antimicrobial, Antikinetoplastid, Antiproliferative and Cytotoxic Assessment

W. Setzer, L. Gille, A. Shchekotikhin, 2020, Molecules.

Design, Synthesis and In Vitro Investigation of Cabozantinib-Based PROTACs to Target c-Met Kinase

D. Andreeva, A. Shchekotikhin, D. Sorokin, 2022, Pharmaceutics.

Discovery of antitumor anthra[2,3-b]furan-3-carboxamides: Optimization of synthesis and evaluation of antitumor properties.

Y. Pommier, M. Kubbutat, M. Preobrazhenskaya, 2016, European journal of medicinal chemistry.

Heterocyclic analogs of 5,12-naphthacenequinone 15*. Synthesis of new anthra[2,3-b]thiophene-3(2)-carboxylic acids

D. Andreeva, A. Shchekotikhin, A. Korolev, 2018, Chemistry of Heterocyclic Compounds.

Indoline-5-Sulfonamides: A Role of the Core in Inhibition of Cancer-Related Carbonic Anhydrases, Antiproliferative Activity and Circumventing of Multidrug Resistance

C. Supuran, D. Vullo, V. De Luca, 2022, Pharmaceuticals.

Heterocyclic analogs of 5,12-naphthacenequinone. 5. Synthesis of 2,3-diamino-1,4-dimethoxyanthraquinone and its heterocyclic derivatives

M. Preobrazhenskaya, A. Shchekotikhin, V. N. Buyanov, 2007 .

Heterocyclic analogs of 5,12-naphthacenequinone. 2. Synthesis of 4,11-dihydroxynaphtho[2,3-f]indazole-5,10-dione and its n-methyl derivatives

M. Preobrazhenskaya, A. Shchekotikhin, O. Anisimova, 2006 .

A facile access to 2-substituted naphtho[2,3-g]quinoline-3-carboxylic acid esters via intramolecular cyclization and PyBOP-promoted functionalization

S. Solovieva, A. Shchekotikhin, A. Tikhomirov, 2020 .

Novel multi-targeting anthra[2,3-b]thiophene-5,10-diones with guanidine-containing side chains: interaction with telomeric G-quadruplex, inhibition of telomerase and topoisomerase I and cytotoxic properties.

V. Mitkevich, J. Balzarini, D. Azhibek, 2014, European journal of medicinal chemistry.

Heterocyclic analogs of 5,12-naphthacenequinone 9*. Study of the synthesis and reactivity of 4,11-dimethoxynaphtho[2,3-f]isatin-5,10-diones

M. Preobrazhenskaya, A. Shchekotikhin, A. Korolev, 2011 .

Heterocyclic analogs of 5,12-naphthacenequinone 7*. Synthesis of naphtho-[2,3-f]isatin-5,10-dione derivatives

M. Preobrazhenskaya, A. Shchekotikhin, Y. Luzikov, 2008 .

Aminoalkylamides of Eremomycin Exhibit an Improved Antibacterial Activity

G. Batta, A. Shchekotikhin, E. Mirchink, 2021, Pharmaceuticals.

Eremomycin pyrrolidide: a novel semisynthetic glycopeptide with improved chemotherapeutic properties

M. Preobrazhenskaya, A. Shchekotikhin, A. Dekhnich, 2018, Drug design, development and therapy.

Amides of pyrrole- and thiophene-fused anthraquinone derivatives: A role of the heterocyclic core in antitumor properties.

M. Moisenovich, D. Andreeva, D. Schols, 2020, European journal of medicinal chemistry.

Synthesis and Characterization of Novel 2-Acyl-3-trifluoromethylquinoxaline 1,4-Dioxides as Potential Antimicrobial Agents

O. Dontsova, V. Danilenko, Md. Shahidul Alam, 2022, Pharmaceuticals.

Heterocyclic Analogues of 5,12-Naphthacenequinone. Part 5. Synthesis of 2,3-Diamino-1,4-dimethoxyanthraquinone and Its Heterocyclic Derivatives.

M. Preobrazhenskaya, A. Shchekotikhin, V. N. Buyanov, 2007 .

Naphthoindazoles. Synthesis of 4,11-Dimethoxynaphtho[2,3-f]indazole-5,10-dione

D. Silaev, A. Shchekotikhin, N. N. Suvorov, 2002 .

Heterocyclic Analogues of 5,12-Naphthacenequinone. Part 2. Synthesis of 4,11-Dihydroxynaphtho[2,3-f]indazole-5,10-dione and Its N-Methyl Derivatives.

M. Preobrazhenskaya, A. Shchekotikhin, O. Anisimova, 2007 .

Synthesis of 1-(ω-aminoalkyl)naphthoindolediones with antiproliferative properties

M. Preobrazhenskaya, A. Shchekotikhin, V. N. Buyanov, 2004 .

Naphthoindoles. 10. Synthesis of 4,11-Dihydroxynaphtho[2,3-f]indole-5,10-dione and Some of Its Derivatives

A. Shchekotikhin, K. F. Turchin, N. N. Suvorov, 2001 .

Heterocyclic Analogs of 5,12-Naphthacenequinone 14*. Synthesis of naphtho[2,3-f]indole-3-carboxylic Acid Derivatives

A. Shchekotikhin, A. Korolev, A. Tikhomirov, 2017, Chemistry of Heterocyclic Compounds.

In Vitro Pharmacological Screening of Essential Oils from Baccharis parvidentata and Lippia origanoides Growing in Brazil

W. Setzer, A. Shchekotikhin, P. Cos, 2022, Molecules.

Synthesis and antiproliferative activity of salicylidenehydrazones based on indole-2(3)-carboxylic acids

A. G. Vasin, A. Shchekotikhin, A. Scherbakov, 2020, Chemistry of Heterocyclic Compounds.

Tri-armed ligands of G-quadruplex on heteroarene-fused anthraquinone scaffolds: Design, synthesis and pre-screening of biological properties.

D. Schols, V. Tsvetkov, A. Shchekotikhin, 2018, European journal of medicinal chemistry.

Thiophene-2-carboxamide derivatives of anthraquinone: A new potent antitumor chemotype.

M. Moisenovich, D. Andreeva, D. Schols, 2021, European journal of medicinal chemistry.

Advances in the Discovery of Anthraquinone-Based Anticancer Agents.

A. Shtil, A. Shchekotikhin, A. Tikhomirov, 2017, Recent patents on anti-cancer drug discovery.

Semisynthetic Amides of Amphotericin B and Nystatin A1: A Comparative Study of In Vitro Activity/Toxicity Ratio in Relation to Selectivity to Ergosterol Membranes

S. Solovieva, A. Shchekotikhin, E. Bychkova, 2023, Antibiotics.

Draft genome sequencing and analysis of mutations of Streptomyces fradiae strain ATCC19609-Olg4R, resistant to (33S)-33-deoxy-33-thiocyanatooligomycin А

A. Shchekotikhin, L. N. Lysenkova, O. B. Bekker, 2017, Russian Journal of Genetics.

New antitumor anthra[2,3-b]furan-3-carboxamides: Synthesis and structure-activity relationship.

P. Kaur, P. Chueh, D. Schols, 2018, European journal of medicinal chemistry.

Synthesis and structure-activity relationship studies of 4,11-diaminonaphtho[2,3-f]indole-5,10-diones.

M. Preobrazhenskaya, A. Shtil, A. Shchekotikhin, 2006, Bioorganic & medicinal chemistry.

3-Aminomethyl derivatives of 4,11-dihydroxynaphtho[2,3-f]indole-5,10-dione for circumvention of anticancer drug resistance.

M. Preobrazhenskaya, A. Shtil, A. Shchekotikhin, 2005, Bioorganic & medicinal chemistry.

β-Hydroxylation of anthraquinone derivatives with benzaldehyde oxime as a source of hydroxyl group

A. Shchekotikhin, A. Korolev, A. Tikhomirov, 2019, Tetrahedron.

Bis(chloroacetamidino)-Derived Heteroarene-Fused Anthraquinones Bind to and Cause Proteasomal Degradation of tNOX, Leading to c-Flip Downregulation and Apoptosis in Oral Cancer Cells

P. Chueh, A. Shchekotikhin, Chia-Wei Weng, 2022, Cancers.

Water-Soluble Heliomycin Derivatives to Target i-Motif DNA.

Zoë A. E. Waller, P. Chueh, A. Shchekotikhin, 2021, Journal of natural products.

Experimental Evaluation of Anticancer Efficiency and Acute Toxicity of Anthrafuran for Oral Administration †

A. Shchekotikhin, A. Tikhomirov, H. Treshalina, 2020, Pharmaceuticals.

Engagement with tNOX (ENOX2) to Inhibit SIRT1 and Activate p53-Dependent and -Independent Apoptotic Pathways by Novel 4,11-Diaminoanthra[2,3-b]furan-5,10-diones in Hepatocellular Carcinoma Cells

P. Chueh, S. Chuang, A. Shchekotikhin, 2019, Cancers.

New anthra[2,3-b]furancarboxamides: A role of positioning of the carboxamide moiety in antitumor properties.

M. Moisenovich, A. Shtil, V. Tsvetkov, 2019, European journal of medicinal chemistry.

Engagement with tNOX ( ENOX 2 ) to Inhibit SIRT 1 and Activate p 53-Dependent and-Independent Apoptotic Pathways by Novel 4 , 11-Diaminoanthra [ 2 , 3-b ] furan-5 , 10-diones in Hepatocellular Carcinoma Cells

P. Chueh, S. Chuang, A. Shchekotikhin, 2019 .

RNA G-Quadruplexes in Kirsten Ras (KRAS) Oncogene as Targets for Small Molecules Inhibiting Translation.

G. Capranico, A. Shchekotikhin, A. Tikhomirov, 2017, Journal of medicinal chemistry.

Heterocyclic Analogs of 5,12-Naphthacene-Quinone. 12. Synthesis of 2-Substituted Derivatives of 4,11-Dimethoxy-5,10-Dioxo-Anthra[2,3-b]Furan-3-Carboxylic Acids

M. Preobrazhenskaya, A. Shchekotikhin, A. Korolev, 2014, Chemistry of Heterocyclic Compounds.

Synthesis and photochemical properties of phenoxy derivatives of anthra[2,3-b]furan-5,10-dione

V. Traven, A. Shchekotikhin, V. A. Barachevskii, 2008 .

Synthesis and Biological Activity of 7(7,11)-Hydroderivatives of Oligomycin A

V. Danilenko, A. Shchekotikhin, A. Korolev, 2018 .

Synthesis, antimicrobial and antiproliferative properties of epi-oligomycin A, the (33S)-diastereomer of oligomycin A

V. Danilenko, A. Shchekotikhin, A. Korolev, 2020, Natural product research.

Glucose starvation greatly enhances antiproliferative and antiestrogenic potency of oligomycin A in MCF-7 breast cancer cells.

A. Shchekotikhin, D. Sorokin, A. Scherbakov, 2021, Biochimie.

Design, synthesis and biomedical evaluation of mostotrin, a new water soluble tryptanthrin derivative

V. Stonik, A. Popov, A. Shchekotikhin, 2020, International journal of molecular medicine.

Heteroarene-fused anthraquinone derivatives as potential modulators for human aurora kinase B.

A. S. Ethayathulla, P. Kaur, A. Shchekotikhin, 2021, Biochimie.

Stereochemistries and Biological Properties of Oligomycin A Diels-Alder Adducts.

A. Shchekotikhin, A. Scherbakov, L. Dezhenkova, 2021, The Journal of organic chemistry.

Photodynamic therapy for ras-driven cancers: targeting G-quadruplex RNA structures with bifunctional alkyl-modified porphyrins.

Francesca D'Este, A. Shchekotikhin, S. Richter, 2020, Journal of medicinal chemistry.

HRAS is silenced by two neighboring G-quadruplexes and activated by MAZ, a zinc-finger transcription factor with DNA unfolding property

A. Shchekotikhin, S. Cogoi, L. Xodo, 2014, Nucleic acids research.

Evaluation of Toxic Properties of New Glycopeptide Flavancin on Rats

A. Shchekotikhin, H. Treshalina, E. Pereverzeva, 2022, Pharmaceuticals.

Bacterial Cell Wall Analogue Peptides Control the Oligomeric States and Activity of the Glycopeptide Antibiotic Eremomycin: Solution NMR and Antimicrobial Studies

G. Batta, P. Herczegh, A. Shchekotikhin, 2021, Pharmaceuticals.

Novel Quinoxaline-2-Carbonitrile-1,4-Dioxide Derivatives Suppress HIF1α Activity and Circumvent MDR in Cancer Cells

A. Shchekotikhin, A. Scherbakov, O. Andreeva, 2018, Cancer investigation.

Toxicological characteristic of novel antitumour multitargeted agent anthrafuran

A. Shchekotikhin, E. Pereverzeva, I. Treschalin, 2017 .

Heterocyclic analogs of 5,12-naphthacenequinone 16*. Synthesis and properties of new DNA ligands based on 4,11-diaminoanthra[2,3-b]thiophene-5,10-dione

D. Andreeva, A. Shchekotikhin, A. Tikhomirov, 2020, Chemistry of Heterocyclic Compounds.

Methods for the Synthesis and Modification of Linear Anthrafurandiones (Review)

M. Preobrazhenskaya, A. Shchekotikhin, A. Tikhomirov, 2014, Chemistry of Heterocyclic Compounds.

Heterocyclic analogs of 5,12-naphthacenequinone 6. Synthesis of 4,11-dimethoxy derivatives of anthra-[2,3-b]thiophene-5,10-dione and anthra[2,3-d]isothiazole-5,10-dione

M. Preobrazhenskaya, A. Shchekotikhin, V. N. Buyanov, 2007 .

Heterocyclic analogs of 5,12-naphthacenequinone. 4. Synthesis of 4,11-dimethoxy-anthra[2,3-d]isoxazole-5,10-dione

M. Preobrazhenskaya, A. Shchekotikhin, Y. Luzikov, 2006 .

Heterocyclic Analogs of 5,12-Naphthacenequinone. 1. Synthesis of Heterocyclic Analogs Starting from 2,3-Diaminoquinizarine

M. Preobrazhenskaya, A. Shchekotikhin, V. N. Buyanov, 2005 .

Annelation of furan rings to arenes

A. Shchekotikhin, A. Tikhomirov, O. Omelchuk, 2016 .

Heterocyclic analogs of 5,12-naphthacene-quinone. 11*. A new method for preparing 4,11-dimethoxyanthra[2,3-b]furan-5,10-dione

M. Preobrazhenskaya, A. Shchekotikhin, A. Korolev, 2013, Chemistry of Heterocyclic Compounds.

Heterocyclic analogs of 5,12-naphthacenequinone 10.* Synthesis of furanoquinizarine and its new derivatives

A. Shchekotikhin, A. Korolev, A. Tikhomirov, 2012, Chemistry of Heterocyclic Compounds.

Abstract 6224: Novel antitumor semi-synthetic heliomycin derivatives direct targeting tNOX-NAD+-SIRT1 axis to activate apoptosis/autophagy, as determined by the cellular thermal shift assay (CETSA)

P. Chueh, A. Shchekotikhin, A. Tikhomirov, 2020 .

Water-soluble 4-(dimethylaminomethyl)heliomycin exerts greater antitumor effects than parental heliomycin by targeting the tNOX-SIRT1 axis and apoptosis in oral cancer cells

Mu-Kuan Chen, P. Chueh, A. Shchekotikhin, 2023, bioRxiv.

Development of a Dosage Form of the New Antitumor Antibiotic Olivamide

A. Shchekotikhin, L. Dezhenkova, A. Tevyashova, 2019, Pharmaceutical Chemistry Journal.

Synthesis of 6″-Modified Kanamycin A Derivatives and Evaluation of Their Antibacterial Properties

I. Osterman, A. Shchekotikhin, A. Tevyashova, 2023, Pharmaceutics.

Guanidino anthrathiophenediones as G-quadruplex binders: uptake, intracellular localization, and anti-Harvey-Ras gene activity in bladder cancer cells.

A. Shchekotikhin, S. Cogoi, L. Xodo, 2013, Journal of medicinal chemistry.

Reductive Elimination of Alkoxy Group in Anthraquinone Derivatives

D. Andreeva, A. Shchekotikhin, A. Tikhomirov, 2022, SSRN Electronic Journal.

Synthesis and fluorescence of anthra[2,3-b]furan-5,10-dione derivatives

V. Traven, A. Shchekotikhin, E. Shevtsova, 2007 .

Subchronic Toxicity Study of Oral Anthrafuran on Rabbits

A. Shchekotikhin, H. Treshalina, E. Pereverzeva, 2021, Pharmaceuticals.

Heterocyclic analogs of 5,12-naphthacenequinone 8.* Synthesis of furano-anthraquinones

M. Preobrazhenskaya, A. Shchekotikhin, Y. Luzikov, 2009 .

Synthesis of thiopheno-quinizarine derivatives

A. Shchekotikhin, L. Kovalenko, Y. Luzikov, 2007 .

Modern Trends of Organic Chemistry in Russian Universities

R. S. Begunov, A. V. Kolobov, K. I. Kobrakov, 2018, Russian Journal of Organic Chemistry.

Quinoxaline 1,4-Dioxides: Advances in Chemistry and Chemotherapeutic Drug Development

A. Shchekotikhin, G. Buravchenko, 2023, Pharmaceuticals.

Eremomycin pyrrolidide: a novel semisynthetic glycopeptide with improved chemotherapeutic properties

M. Preobrazhenskaya, A. Shchekotikhin, A. Dekhnich, 2018, Drug design, development and therapy.

eremomycin pyrrolidide: a novel semisynthetic glycopeptide with improved chemotherapeutic properties

A. Shchekotikhin, A. Dekhnich, E. Mirchink, 2018 .

Supplemental Data

V. Danilenko, I. Godovikov, A. Shchekotikhin, 2012 .

Bioinformatic analysis of genes of Streptomyces xinghaiensis (fradiae) ATCC 19609 with a focus on mutations conferring resistance to oligomycin A and its derivatives.

V. Danilenko, A. Shchekotikhin, O. B. Bekker, 2020, Journal of global antimicrobial resistance.

Draft genome sequencing and analysis of mutations of Streptomyces fradiae strain ATCC19609-Olg4R, resistant to (33S)-33-deoxy-33-thiocyanatooligomycin А

V. Danilenko, A. Shchekotikhin, O. B. Bekker, 2017, Russian Journal of Genetics.

Neurotoxic properties of new antitumor agent anthrafuran

A. Shchekotikhin, I. Treshchalin, E. Pereverzeva, 2019, Russian Journal of Biotherapy.

Experimental Evaluation of the Hypersensitivity Reactions of a New Glycopeptide Antibiotic Flavancin in Animal Models

A. Shchekotikhin, S. A. Dovzhenko, M. B. Kobrin, 2023, Pharmaceuticals.

Naphthoindoles. 8. Electrophilic substitution reactions of 4,11-dimethyxynaphtho[2,3-f]indole-5,10-dione

A. Shchekotikhin, K. F. Turchin, N. N. Suvorov, 1998 .

The chemistry of heterocycles in the 21st century

A. A. Larin, I. V. Dyachenko, Y. Gorbunova, 2024, Russian Chemical Reviews.

New heteroarene-fused anthraquinones: Synthesis and PyBOP-mediated amination

A. Shchekotikhin, A. Tikhomirov, Valeria A. Litvinova, 2023, Tetrahedron.