Department of Medical Chemistry
(Created: Dec. 30, 2018 )
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- 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:
- Directed modification of natural compounds (alkaloids, terpenoids, coumarins, flavonoids, etc.)
- 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.
- 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:
- STAFF
Staff
- PUBLICATIONS
Laboratory staff publications (DB NIOCh)
Reviews, Articles
2021- V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
Unexpected ring opening during the imination of camphor-type bicyclic ketones
European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=2.888 - V. Fomenko, M. Blokhin, S. Kuranov, M. Khvostov, D. Baev, M.S. Borisova, O. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
Triterpenic Acid Amides as a Promising Agent for Treatment of Metabolic Syndrome
Sci. Pharm. 2021, 89(1), 4 doi:10.3390/scipharm89010004
2020- K. Kovaleva, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, O. Lavrik, N. Salakhutdinov
Dehydroabietylamine-based thiazolidin-4-ones and 2-thioxoimidazolidin-4-ones as novel tyrosyl-DNA phosphodiesterase 1 inhibitors
Molecular Diversity (2020), Published: 24 August 2020 doi:10.1007/s11030-020-10132-z, IF=2.13 - 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 - 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. - 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 - 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
- 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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- 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 - 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 - 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 - 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
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937 - 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
- 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
A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861 - 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 - 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
- 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 - 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 - 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
- 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 - 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 - 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 - 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
- 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
- V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov