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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
of Siberian Branch of Russian Academy of Sciences

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Employee:  Ardashov Oleg Vasilievich
Positions:  Senior Researcher (Cand. Chem.), LPhAC


 


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Personal publicalions (DB NIOCh)


2022

Reviews, articles

  1. A. Kotlyarova, A.V. Podturkina, A.V. Pavlova, D.S. Gorina, A.V. Lastovka, O.V. Ardashov, A.D. Rogachev, A.E. Izyurov, A.B. Arefieva, A.V. Kulikov, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov, Yu. Sidorova
    A Newly Identified Monoterpenoid-Based Small Molecule Able to Support the Survival of Primary Cultured Dopamine Neurons and Alleviate MPTP-Induced Toxicity In Vivo
    Molecules 2022, 27(23), 8286; doi:10.3390/molecules27238286, IF=4.927
  2. O.V. Ardashov, D.V. Korchagina, I.Yu. Bagryanskaya, K.P. Volcho, N.F. Salakhutdinov
    (1S,5R)-6,6-Dimethyl-4-(((1S,2S,5S)-2,6,6-trimethyl-4-oxobicyclo[3.1.1]heptan-2-yl)methyl)bicyclo[3.1.1]hept-3-en-2-one
    Molbank 2022, 2022(4), M1465 doi:10.3390/M1465
  3. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472

2021

Reviews, articles

  1. A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
    Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.706

2019

Reviews, articles

  1. 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

2018

Reviews, articles

  1. A.Yu. Sidorenko, I.V. Il'ina, A.V. Kravtsova, A. Aho, O.V. Ardashov, N.S. Li-Zhulanov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of chiral isobenzofurans from 3-carene in the presence of modified clays
    Molecular Catalysis, 2018, V. 459, Pp 38-45 doi:10.1016/j.mcat.2018.07.025
  2. A.Yu. Sidorenko, A.V. Kravtsova, J. Warna, A. Aho, I. Heinmaa, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays
    Molecular Catalysis, 2018, V. 453, Pp. 139-148 doi:10.1016/j.mcat.2018.05.007

2017

Reviews, articles

  1. M.V. Trushin, R.G. Khamidullina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov
    The action of monoterpenoids with promising antiparkinsonian activity on fertility of Drosophila melanogaster
    Marmara Pharmaceutical Journal, 2017, V. 21, N 4, 2017, Pp 987-991 doi:10.12991/mpj.2017.29
  2. I. Il'ina, A. Pavlova, D. Korchagina, O. Ardashov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of monoterpenoid-derived alkyl-substituted chiral hexahydro-2H-chromenes
    Medicinal Chemistry Research, 2017, V. 26, N 7, pp 1415-1426 doi:10.1007/s00044-017-1847-4, IF=1.276
  3. E. Valdman, I. Kapitsa, Е. Ivanova, T. Voronina, O. Ardashov, K. Volcho, V. Khazanov, N. Salakhutdinov
    Evolution of anti-parkinsonian activity of monoterpenoid (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in various in vivo models
    European Journal of Pharmacology, 2017, V. 815, Pp 351-363 doi:10.1016/j.ejphar.2017.09.022, IF=2.895

2016

Reviews, articles

  1. A.V. Pavlova, E.V. Nazimova, O.S. Mikhal'chenko, I.V. Il'ina, D.V. Korchagina, O.V. Ardashov, E.A. Morozova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2H-Chromen-4,8-Diols Containing Thiophene Substituents
    Chemistry of Natural Compounds, , 2016, V. 52, N 5, pp 813-820 doi:10.1007/s10600-016-1785-2, IF=0.472
  2. A. Sokolova, A. Pavlova, N. Komarova, O. Ardashov, A. Shernyukov, Yu. Gatilov, O. Yarovaya, T. Tolstikova, N. Salakhutdinov
    Synthesis and analgesic activity of new α-truxillic acid derivatives with monoterpenoid fragments
    Medicinal Chemistry Research, 2016, V. 25, N 8, pp 1608-1615 doi:10.1007/s00044-016-1593-z, IF=1.435

2015

Reviews, articles

  1. K. Ponomarev, A. Pavlova, E. Suslov, O. Ardashov, D. Korchagina, A. Nefedov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of new compounds combining azaadamantane and monoterpene moieties
    Medicinal Chemistry Research, 2015, V. 24, N 12, pp 4146-4156 doi:10.1007/s00044-015-1464-z, IF=1.401
  2. O.V. Ardashov, Yu. S. Demidova, D.V. Korchagina, K.P. Volcho, I.L. Simakova, N.F. Salakhutdinov
    The First Synthesis of (4S,5R,6R)-5,6-Dihydroxy-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic Acid
    Helvetica Chimica Acta, V. 98, N 10, Pp 1442-1455 doi:10.1002/hlca.201500125, IF=1.138
  3. O. V. Ardashov, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov
    Synthesis of 10-Carbonyl and 10-Carboxylic Derivatives of para -Mentha-1,8-Diene-5,6-Diol
    Chemistry of Natural Compounds, 2015, V. 51, N 3, pp 483-487 doi:10.1007/s10600-015-1320-x, IF=0.509

2014

Reviews, articles

  1. Yu.S. Demidova, O.V. Ardashov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Isomerization of bicyclic terpene epoxides into allylic alcohols without changing of the initial structure
    Journal of Molecular Catalysis A: Chemical, 2014, V. 388–389, Pp 162–166. Special Issue on Biomass Catalysis. doi:10.1016/j.molcata.2013.09.016, IF=3.678
  2. О.В. Ардашов, К.П. Волчо, Н.Ф. Салахутдинов
    Синтез гидроксипроизводных лимонена
    Успехи химии. 2014. Т. 83. № 4. С. 281-298. (Synthesis of hydroxy derivatives of limonene/ O V Ardashov, K P Volcho and N F Salakhutdinov// Russ. Chem. Rev. 2014, 83(4), 281-298. doi:10.1070/RC2014v083n04ABEH004383), IF=2.582
  3. K. Volcho, Ardashov, O. Mikhalchenko, I. Il'ina, N. Salakhutdinov
    Synthetic Transformations of para-Menthane Monoterpenoids: New Way to Elaboration of Medicines for Mental Health
    Chem. Listy, 108, s120-s121 (2014)., IF=0.195

2013

Reviews, articles

  1. M.V. Trushin, I.A. Arkharova, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov
    Genotoxicological safety assessment of a new antiparkinsonian substance ((1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol)
    World Journal of Medical Sciences, 2013, Т. 8, N 4, С. 355-358. doi:10.5829/idosi.wjms.2013.8.4.1123
  2. О.В. Ардашов, А.М. Генаев, Г.Е. Сальников, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов
    Синтез и установление строения диастереомеров (1R,2R,6S)-6-[1-({[(1R,S)-1-(1-адамантил)этил]амино}метил)винил]-3-метилциклогекс-3-ен-1,2-диола
    Журнал органической химии, 2013, Т. 49, N 10, С.1456-1459. (Synthesis and structure determination of diastereoisomeric (1R,2R,6S)-6-[1-({[(1R,S))-1-(1-adamantyl)ethyl]amino}prop-1-en-2-yl)-3-methylcyclohex-3-ene-1,2-diols/ O. V. Ardashov, A. M. Genaev, G. E. Sal’nikov, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1433-1436 doi:10.1134/S1070428013100059), IF=0.513
  3. O.V. Ardashov, A.V. Pavlova, D.V. Korchagina, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    3-Methyl-6-(prop-1-en-2-yl) cyclohex-3-ene-1,2-diol: the Importance of Functional Groups for Antiparkinsonian Activity
    Medicinal Chemistry, 2013, V. 9, N 5, P. 731-739. doi:10.2174/1573406411309050013, IF=1.373
  4. M. Stekroval, N. Kumarl, P. Maki-Arvelal, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective Preparation of trans-Carveol over Ceria Supported Mesoporous Materials MCM-41 and SBA-15
    Materials, 2013, V.6, N 5, P. 2103-2118. doi:10.3390/ma6052103, IF=2.246
  5. O.V. Ardashov, A.V. Pavlova, D.V. Korchagina, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Antiparkinsonian activity of some 9-N-, O-, S- and C-derivatives of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 5, P. 1082-1087. doi:10.1016/j.bmc.2013.01.003, IF=2.903
  6. О.В. Ардашов, Е.В. Хаид, О.С. Михальченко, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов
    Первый синтез пара-мента-1,8-диенового триола
    Известия АН. Серия химическая, 2013, N 1, С. 172-175. (First synthesis of p-mentha-1,8-diene triol/ O. V. Ardashov, E. V. Khaid, O. S. Mikhal’chenko, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 171-174 doi:10.1007/s11172-013-0025-1), IF=0.423

2011

Reviews, articles

  1. O.V. Ardashov, A.V. Pavlova, I.V. Il'ina, E.A. Morozova, D.V. Korchagina, E.V. Karpova, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Highly potent activity of (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in animal models of Parkinson's disease
    J. Med. Chem., 2011, V. 54, N 11, 3866-74. doi:10.1021/jm2001579, IF=5.206
  2. O.V. Ardashov, V.V. Zarubaev, A.A. Shtro, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Antiviral activity of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol and its derivatives against influenza A(H1N1)2009 virus
    Lett. Drug Des. Discov., 2011, V. 8, N 4, 375-380. doi:10.2174/157018011794839411, IF=0.667

2010

Reviews, articles

  1. Т.Г. Толстикова, А.В. Павлова, Е.А. Морозова, О.В. Ардашов, И.В. Ильина, К.П. Волчо, Н.Ф. Салахутдинов, Г.А. Толстиков
    Высокоэффективное противопаркинсоническое средство нового структурного типа
    Доклады Академии наук, 2010, Т. 435, N 5, C. 708–710. (A highly effective antiparkinsonian drug of a new structural type/ T. G. Tolstikova, A. V. Pavlova, Ye. A. Morozova, O. V. Ardashov, I. V. Il’ina, K. P. Volcho, N. F. Salakhutdinov, G. A. Tolstikov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 398-399. doi:10.1134/S0012496610060074)
  2. О.В. Ардашов, А.М. Генаев, И.В. Ильина, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов
    Гидрирование и конформационный анализ (1R,2R,6S)-6-метилэтенил-3-метилциклогекс-3-ен-1,2-диола
    Журнал органической химии, 2010, Т. 46, N 12, C. 1786-1789. (Hydrogenation and conformational analysis of (1R,2R,6S)-3-methyl-6-(1-methylethenyl)cyclohex-3-ene-1,2-diol/ O.V. Ardashov, A.M. Genaev, I.V. Il'ina, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, G.A. Tolstikov// RUSS J ORG CHEM+, 2010, V. 46, N 12, pp 1786-1789. doi:10.1134/S1070428010120043), IF=0.524
  3. А.В. Павлова, Т.Г. Толстикова, Е.А. Морозова, О.В. Ардашов, И.В. Ильина, К.П. Волчо, Н.Ф. Салахутдинов
    Гидроксикетоны пара-ментанового ряда – перспективные анальгетики
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 495-497. (Hydroxyketones of para-Menthane Series as Promising Analgetics/ A.V. Pavlova, T.G. Tolstikova, E.A. Morozova, O.V. Ardashov, I.V. Ilyina, K.P. Volcho, N.F. Salakhutdinov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp.423-455. (in russian))

2009

Reviews, articles

  1. Т.Г. Толстикова, А.В. Павлова, М.П. Долгих, И.В. Ильина, О.В. Ардашов, К.П. Волчо, Н.Ф. Салахутдинов, Г.А. Толстиков
    Новый высокоэффективный противосудорожный агент – (4S,5R,6R)-пара-мента-1,8-диен-5,6-диол
    Доклады Академии наук (Биология), 2009, Т. 429, № 1, С. 139-141. ((4S,5R,6R)-para-mentha-1,8-dien-5,6-diol is a new highly effective anticonvulsant agent/ T.G. Tolstikova, A.V. Pavlova, M.P. Dolgikh, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, G.A. Tolstikov// Doklady Biological Sciences, 2009, V. 429, N 1, pp 494-496. doi:10.1134/S0012496609060039)
  2. О.В. Ардашов, И.В. Ильина, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов
    Необычные продукты взаимодействия вербенона и вербенола с N-бромсукцинимидом в присутствии воды.
    Журнал органической химии, 2009, Т. 45, N 10, С. 1469-1472. (Unusual products of the reactions of verbenone and verbenol with N-bromosuccinimide in the presence of water/ O.V. Ardashov, I.V. Il'ina, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov// Russian Journal of Organic Chemistry, 2009, V. 45, N 10, pp 1452-1455. doi:10.1134/S1070428009100054), IF=0.556

2007

Reviews, articles

  1. O.V. Ardashov, I.V. Il’ina, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Unusual α-hydroxyaldehyde with a cyclopentane framework from verbenol epoxide
    Mendeleev Commun., 2007, V. 17, N 5, 303-305. doi:10.1016/j.mencom.2007.09.020, IF=0.712



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