Laboratory of Directed Transformations of Natural Compounds
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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
 of Siberian Branch of Russian Academy of Sciences

Department of Medical Chemistry

(Created: Dec. 30, 2018 )

 

Suslov E.V.


Head of Lab. 
Ph.D. Evgeny V. Suslov
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.
 
Resercher ares

The main activities of the laboratory are:

  • Search and creation of new highly effective, low-toxic domestic drugs for the treatment and prevention of socially significant diseases. The basis of the creation of medicinal agents are such approaches as:
    1. Directed modification of natural compounds (alkaloids, terpenoids, coumarins, flavonoids, etc.)
    2. Analysis and modification of structures of known natural biologically active compounds;
  • Creation of highly efficient and safe drug delivery systems based on natural compounds and their derivatives;
  • Development of new regioselective and stereoselective approaches and synthesis methods for the modification of natural compounds for the production of target substances;
  • Improving the structure of leading compounds in order to increase their pharmacodynamic and pharmacokinetic characteristics, as well as activity and selectivity, using for this purpose techniques such as the synthesis of structural analogs based on the principle of three-dimensional pharmacophore similarity, changing the conformational mobility of the original molecule, bioisteric replacement, changing the balance of lipophilic and hydrophilic groups, creating peptidomimetics, changing metabolizable groups, etc.

Partners of the laboratory:

  • Novosibirsk State University;
     
  • Moscow State University;

  • School of Chemistry, University of Auckland (New Zealand);
     
  • Institute of Chemical Biology and Fundamental Medicine;
     
  • Institute of Catalysis;
     
  • Abo University (Finland);
     
  • St. Petersburg Pasteur Research Institute of Epidemiology and Microbiology;
     
  • State Research Center of Virology and Biotechnology VECTOR.
     

 

STAFF

Staff

№ Employee Position Room Phone Phone in. email Publications
by years
1 Suslov Evgeny Vladimirovich Senior Researcher (Cand. Chem.) 215, 103 330-88-51, 330-88-70 3-40, 4-46 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Mozhaitsev Evgeny Sergeevich Researcher (Cand. Chem.) 103 330-88-70 4-46 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Ponomarev Konstantin Yurievich Researcher (Cand. Chem.) 103 330-88-70 4-46 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Gladkova Elizaveta Dmitrievna Junior Researcher 204 330-88-70 2-21 This email address is being protected from spambots. You need JavaScript enabled to view it.
5 Podturkina Alexandra Vladimirovna Junior Researcher 129 330-88-70 3-96 This email address is being protected from spambots. You need JavaScript enabled to view it.
6 Filimonov Alexander Sergeevich Junior Researcher 204 330-88-70 2-21 This email address is being protected from spambots. You need JavaScript enabled to view it.
7 Brusentseva Olga Igorevna Junior Researcher (Cand. Chem.) 101 330-56-50 3-86 This email address is being protected from spambots. You need JavaScript enabled to view it.
PHD Students
8 Munkuev Aldar Ayurovich Junior Researcher 103 330-88-70 4-46 This email address is being protected from spambots. You need JavaScript enabled to view it.

PUBLICATIONS
 

 

Laboratory staff publications (DB NIOCh)

Reviews, Articles


2023
  1. M.V. Khvostov, E.D. Gladkova, S.A. Borisov, M.S. Fedotova, N.A. Zhukova, M.K. Marenina, Yu.V. Meshkova, N. Valutsa, O.A. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
    9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation
    Pharmaceutics 2023, 15(1), 44; doi:10.3390/pharmaceutics15010044, IF=6.525
  2. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  3. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927

2022
  1. D.V. Reshetnikov, I.D. Ivanov, D.S. Baev, T.V. Rybalova, E.S. Mozhaitsev, S.S. Patrushev, V.A. Vavilin, T.G. Tolstikova, E.E. Shults
    Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
    Molecules 2022, 27(24), 8787 doi:10.3390/molecules27248787, IF=4.927
  2. OPTIMIZATION OF THE SYNTHESIS OF 2-ADAMANTANECARBOXYLIC ACID/ Munkuev A.A., Sheshkovas A.Zh., Suslov E.V., Volcho K.P., Salakhutdinov N.F.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 612-616. doi:10.15372/CSD2022424
  3. N,N-SUBSTITUTED BISPIDINES AS LIGANDS OF METAL COMPLEX CATALYSTS FOR THE ETHYNYLATION REACTION/ Mozhaitsev E.S., Okhina A.A., Ponomarev K.Yu., Rogachev A.D., Suslov E.V., Volcho K.P., Salakhutdinov N.F., Vatsadze S.Z.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 595-599. doi:10.15372/CSD2022422
  4. M.V. Khvostov, E.D. Gladkova, S.A. Borisov, M.S. Fedotova, N.A. Zhukova, M.K. Marenina, Yu.V. Meshkova, O.A. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
    Study of Hypoglycemic Activity of Novel 9-N-alkyltetrahydroberberine Derivatives
    Int. J. Mol. Sci. 2022, 23(22), 14186 doi:10.3390/ijms232214186, IF=6.208
  5. A.S. Filimonov, O.I. Yarovaya, A.V. Zaykovskaya, N.B. Rudometova, D.N. Shcherbakov, V.Yu. Chirkova, D.S. Baev, S.S. Borisevich, O.A. Luzina, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(10), 2154 doi:10.3390/v14102154, IF=5.817
  6. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  7. Штро А.А., Галочкина А.В., Николаева Ю.В., Гаршинина А.В., Разгуляева Д.Н., Пономарев К.Ю., Можайцев Е.С., Суслов Е.В., Волчо К.П., Салахутдинов Н.Ф.
    Противовирусная активность производных адамантанов в отношении респираторно-синцитиального вируса
    Медицинский академический журнал. 2022. Т. 22. № 2. С. 115-123. doi:10.17816/MAJ108808
  8. A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
    Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
  9. K. Kovaleva, O. Oleshko, O. Yarovaya, S. Cheresiz, A. Zakharenko, K. Ponomarev, O. Lavrik, A. Pokrovsky, N. Salakhutdinov
    Inhibition of the DNA repair enzyme TDP1 by the resin acid derivatives as a new way to increase the efficiency of glioblastoma chemotherapy
    AIP Conference Proceedings 2390, 020036 (2022) doi:10.1063/5.0069407
  10. D.P. Krut'ko, A.V. Medved'ko, K.A. Lyssenko, A.V. Churakov, A.I. Dalinger, M.A. Kalinin, A.O. Gudovannyy, K.Yu. Ponomarev, E.V. Suslov, S.Z. Vatsadze
    Bispidine Platform as a Tool for Studying Amide Configuration Stability
    Molecules 2022, 27(2), 430 doi:10.3390/molecules27020430, IF=4.927
  11. A.Yu. Sidorenko, Yu.M. Kurban, A.V. Kravtsova, I.V. I'ina, N.S. Li-Zhulanov, D.V. Korchagina, J.E. Sanchez-Velandia, A. Aho, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds
    Applied Catalysis A: General, V. 629, 5 January 2022, 118395 doi:10.1016/j.apcata.2021.118395, IF=5.723
  12. V.A. Stepanova, S.S. Patrushev, T.V. Rybalova, E.E. Shults
    Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent
    Journal of Molecular Structure, V.1247, 5 January 2022, 131373 doi:10.1016/j.molstruc.2021.131373, IF=3.841
  13. V.V. Chernyshov, O.I. Yarovaya, Ia.L. Esaulkova, E. Sinegubova, S.S. Borisevich, I.I. Popadyuk, V.V. Zarubaev, N.F. Salakhutdinov
    Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses
    Bioorganic & Medicinal Chemistry Letters, V. 55, 1 January 2022, 128465 doi:10.1016/j.bmcl.2021.128465, IF=2.94

2021
  1. E.V. Suslov, K.Yu. Ponomarev, O.S. Patrusheva, S.O. Kuranov, A.A. Okhina, A.D. Rogachev, A.A. Munkuev, R.V. Ottenbacher, A.I. Dalinger, M.A. Kalinin, S.Z. Vatsadze, K.P. Volcho, N.F. Salakhutdinov
    Novel Bispidine-Monoterpene Conjugates—Synthesis and Application as Ligands for the Catalytic Ethylation of Chalcones
    Molecules, 2021, 26(24), 7539 doi:10.3390/molecules26247539, IF=4.411
  2. M. Neganova, Yu. Aleksandrova, E. Suslov, E. Mozhaitsev, A. Munkuev, D. Tsypyshev, M. Chicheva, A. Rogachev, O. Sukocheva, K. Volcho, S. Klochkov
    Novel Multitarget Hydroxamic Acids with a Natural Origin CAP Group against Alzheimer’s Disease: Synthesis, Docking and Biological Evaluation
    Pharmaceutics, 2021, 13(11), 1893 doi:10.3390/pharmaceutics13111893, IF=6.321
  3. E.D. Gladkova, O.A. Luzina, N.F. Salakhutdinov
    Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine
    Chemistry of Natural Compounds, 2021, V. 57, N 6, Pp 1062-1065 doi:10.1007/s10600-021-03550-4, IF=0.809
  4. Azaadamantanes, a New Promising Scaffold for Medical Chemistry/ E. V. Suslov, K. Yu. Ponomarev, K. P. Volcho, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2021, V. 47, N 6, Pp. 11331154 doi:10.1134/S1068162021060236, IF=0.796
  5. Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN, IF=6.926
  6. A. A. Munkuev,E. S. Mozhaitsev,A. A. Chepanova,E. V. Suslov,D. V. Korchagina,O. D. Zakharova,E. S. Ilina,N. S. Dyrkheeva,A. L. Zakharenko,J. Reynisson,K. P. Volcho,N. F. Salakhutdinov ,O. I. Lavrik
    Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments
    Molecules 2021, 26(11), 3128; doi:10.3390/molecules26113128, IF=4.411
  7. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863

2020
  1. S. Kuranov, O. Luzina, M. Khvostov, D. Baev, D. Kuznetsova, N. Zhukova, P. Vassiliev, A. Kochetkov, T. Tolstikova, N. Salakhutdinov
    Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
    Pharmaceuticals 2020, 13(11), 404 doi:10.3390/ph13110404, IF=4.285
  2. А. Чепанова, Н.С. Ли-Жуланов, Т.А. Кургина, А.Л. Захаренко, О.Д. Захарова, К.П. Волчо, Н.Ф. Салахутдинов, О.И. Лаврик
    Разработка ингибиторов tdpi на основе производных хроменов как потенциальных противораковых препаратов
    Гены и Клетки. 2020. Т. 15. № S3. С. 68-69.
  3. S.O. Kuranov, O.A. Luzina, N.F. Salakhutdinov
    FFA1 (GPR40) Receptor Agonists Based on Phenylpropanoic Acid as Hypoglycemic Agents: Structure–Activity Relationship
    Russian Journal of Bioorganic Chemistry, 2020, V. 46, N 6, Pp 972-988 doi:10.1134/S1068162020060151, IF=0.682
  4. Conjugates of Bispidine and Monoterpenoids as Ligands of Metal Complex Catalysts for the Henry Reaction/ E. S. Mozhaitsev, K. Y. Ponomarev, O. S. Patrusheva, A. V. Medvedko, A. I. Dalinger, A. D. Rogachev, N. I. Komarova, D. V. Korchagina, E. V. Suslov, K. P. Volcho, N. F. Salakhutdinov, S. Z. Vatsadze// Russian Journal of Organic Chemistry, 2020, V.56, N 11, Pp 1969-1981 doi:10.1134/S1070428020110123, IF=0.624
  5. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
    New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
    RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
  6. Yu.S. Demidova, E.S. Mozhaitsev, E.V. Suslov, A.A. Nefedov, A.A. Saraeva, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, I.L. Simakova, D.Yu. Murzin
    Menthylamine synthesis via gold-catalyzed hydrogenation of menthone oxime
    Applied Catalysis A: General, 2020, V. 605, 117799 doi:10.1016/j.apcata.2020.117799, IF=5.6
  7. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  8. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  9. A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Effect of bispidine containing monoterpenoid moieties on physical performance in mice
    2020 Cognitive Sciences, Genomics and Bioinformatics (CSGB), Novosibirsk, Russia, 2020, pp. 114-117 doi:10.1109/CSGB51356.2020.9214697
  10. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  11. N.S. Li-Zhulanov, A.V. Pavlova, D.V. Korchagina, Yu.V. Gatilov, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis of 1,3-Oxazine Derivatives Based on (-)-Isopulegol using the Ritter Reaction and Study of their Analgesic Activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 936-941 doi:10.1007/s10593-020-02753-x, IF=1.519
  12. O.I. Brusentseva, Yu.V. Kharitonov, M.P. Dolgikh, T.G. Tolstikova, E.E. Shul'ts
    Synthesis and Analgesic Activity Assessment of Furanolabdanoid Conjugates with Glucuronic Acid
    Chemistry of Natural Compounds, 2020, V. 56, N 4, Pp 678-687 doi:10.1007/s10600-020-03119-7, IF=0.653
  13. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
    Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
    Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567
  14. V.V. Chernyshov, O.I. Yarovaya, R.Yu. Peshkov, N.F. Salakhutdinov
    Synthesis of cyclic D-(+)-camphoric acid imides and study of their antiviral activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 763-768 doi:10.1007/s10593-020-02728-y, IF=1.491
  15. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  16. O.I. Brusentzeva, Yu.V. Kharitonov, D.S. Fadeev, E.E. Shults
    Synthesis and spectroscopic studies of furan-bridged polyazamacrocycles through 15,16-bis((prop-2-ynylamino)methyl)labdatriene transformations
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2020, 96, N 3-4, Pp 245-250 doi:10.1007/s10847-019-00965-z, IF=1.56
  17. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
    Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
  18. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
    Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
  19. A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    The effect of 3,7-diazabicyclo[3.3.1]nonanes containing monoterpenoid moieties on the physical activity of mice
    Journal of research in pharmacy, 2020, V. 24, N 2, Pp 196-204 doi:10.35333/jrp.2020.136
  20. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
    Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
    Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
  21. Analytical Control of Impurities and Active Components in (-)-Isopulegol Derivative - Highly Potent Analgesic Agent/ Lastovka A.V, Fadeeva V.P., Il'ina I.V., Salakhutdinov N.F.// Pharmaceutical Chemistry Journal doi:10.1007/s11094-020-02176-0, IF=0.538

2019
  1. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
    Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
  2. V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
    The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
    Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
  3. A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
    Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
    Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789
  4. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
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    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  5. Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104, IF=0.794
  6. O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
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    ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
  7. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  8. Synthesis and Hypoglycemic Activity of Aryl(Hetaryl)Propenoic Cyanopyrrolidine Amides/ S. O. Kuranov, M. E. Blokhin, S. A. Borisov, M. V. Khvostov, O. A. Luzina, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 5, pp 374-380 doi:10.1134/S1068162019050078, IF=0.794
  9. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
    Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
    Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
  10. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  11. Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y, IF=1.014
  12. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  13. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  14. N.S. Li-Zhulanov, I.V. Il’ina, A. Chicca, P. Schenker, O.S. Patrusheva, E.V. Nazimova, D.V. Korchagina, M. Krasavin, K.P. Volcho, N.F. Salakhutdinov
    Effect of chiral polyhydrochromenes on cannabinoid system
    Medicinal Chemistry Research, 2019, V. 28, N 4, pp 450-464 doi:10.1007/s00044-019-02294-9, IF=1.72
  15. Synthesis of diazaadamantanes from 1,5-dimethylbispidinone and some natural ketones/ Suslov E.V.1, Ponomarev K. Yu.1, Korchagina D.V.1, Volcho K.P.1,2, Salakhutdinov N.F.// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 601-605 doi:10.1007/s11172-019-2461-z, IF=1.014
  16. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746



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