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Федеральное государственное бюджетное учреждение науки
Новосибирский институт органической химии им. Н.Н. Ворожцова
Сибирского отделения Российской академии наук

Поздразделение:  Лаборатория физиологически активных веществ (ЛФАВ)
Руководитель:  зав. лабораторией (дхн) Салахутдинов Нариман Фаридович


 

Публикации (по IF ) сотрудников подразделения (БД НИОХ СО РАН)

  1. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
     
  2. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
     
  3. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
     
  4. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-pot monoterpene alcohol amination over Au/ZrO2 catalyst: Effect of the substrate structure
    Journal of Catalysis, 2018, V. 360, Pages 127-134 doi:10.1016/j.jcat.2018.01.020, IF=6.759
     
  5. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
     
  6. N.E. Polyakov, T.V. Leshina, N.F. Salakhutdinov, T.A. Konovalova, L.D. Kispert
    Antioxidant and redox properties of supramolecular complexes of carotenoids with beta-glycyrrhizic acid
    Free Radical Bio. Med., 2006, V. 40, N 10, 1804-1809. doi:10.1016/j.freeradbiomed.2006.01.015, IF=5.399
     
  7. 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
     
  8. 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
     
  9. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
     
  10. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    A new synthetic varacin analogue, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), decreased hereditary catalepsy and increased the BDNF gene expression in the hippocampus in mice
    Psychopharmacology, 2012, V. 221, N 3, 469–478. doi:10.1007/s00213-011-2594-8, IF=4.77
     
  11. A. Sidorenko, A. Kravtsova, A. Aho, I. Heinmaa, V. Agabekov, K. Volcho, N. Salakhutdinov, D. Murzin
    Acid-modified Halloysite Nanotubes as a Stereoselective Catalyst for Synthesis of 2H-Chromene Derivatives by the Reaction of Isopulegol with Aldehydes
    ChemCatChem, 2018, V. 10, N 18, Pp 3950-3954 doi:10.1002/cctc.201800974, IF=4.674
     
  12. I.L. Simakova, Yu.S. Demidova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, A. Simakov
    Gold catalyzed one-pot myrtenol amination: Effect of catalyst redox activationOriginal Research Article
    Сatalysis Today, V. 279, Part 1, 1 January 2017, Pages 63-70 doi:10.1016/j.cattod.2016.01.044, IF=4.636
     
  13. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
     
  14. N.F. Salakhutdinov, L.N. Rogoza, G.A. Tolstikov
    Hypercholesteremia: Chemical Aspect of Approach
    Curr. Med. Chem., 2011. V. 18, N 26, pp 4076-4105. doi:10.2174/092986711796957248, IF=4.63
     
  15. И.И. Попадюк, О.В. Саломатина, Н.Ф. Салахутдинов
    Современные подходы к модификации желчных кислот с целью синтеза соединений, обладающих ценными физико-химическими и биологическими свойствами
    Успехи химии. 2017. Т. 86. № 5. С. 388-443 (Modern approaches to modification of bile acids for the synthesis of compounds possessing valuable physicochemical and biological properties/ I.I. Popadyuk, O.V. Salomatina, N. F. Salakhutdinov// Russian Chemical Reviews, 2017, V. 86, N 5, Pp 388-443 doi:10.1070/RCR4683), IF=4.58
     
  16. Ju.A. Sidorova, K.P. Volcho, N.F. Salakhutdinov
    Neuroregeneration in Parkinson’s Disease: From Proteins to Small Molecules
    Current Neuropharmacology, 2019,V. 17 , N 3 , Pp. 268 - 287 doi:10.2174/1570159X16666180905094123, IF=4.568
     
  17. 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
     
  18. E.A. Kulikova, O.S. Kozhevnikova, A.V. Kulikov, N.G. Kolosova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, D.V. Telegina
    Alterations of STEP46 and STEP61 Expression in the Rat Retina with Age and AMD-Like Retinopathy Development
    Int. J. Mol. Sci. 2020, 21(15), 5182 doi:10.3390/ijms21155182, IF=4.556
     
  19. A.V. Markov, Al.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
    Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556
     
  20. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov,O I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
     


 

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16-07-2020

Категория: Объявления о защитах диссертаций

Черемных Кирилл Павлович, 18.09.2020 в 11-00 Защита диссертации Черемных К.П. «Синтез гетероциклических производных природных и синтетических антранилатов на основе алкинонов, полученных в условиях металлокомплексного катализа»




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