Laboratory of Nitrogen Compounds (LNC)

Head - Cand. of Chemical Sciences
Igor A. Kirilyuk
Phone: 8(383) 330-7387

e-mail:This email address is being protected from spambots. You need JavaScript enabled to view it.

The Laboratory of Nitrogen Compounds (LNC) was organized by professor Leonid B. Volodarsky on the basis of research group founded in 1974. Since 1998 the laboratory is headed by professor Igor A. Grigor’ev, who was simultaneously the director of the Novosibirsk Institute of Organic Chemistry SB RAS since 2002 to 2012.

The subject of research activities of the LNC originated from studies of chemistry of hydroxylamine bifunctional organic derivatives. Further evolution of these research resulted in development of original methods for synthesis of various heterocyclic compounds, oximes, nitrones and stable nitroxides.

In 1994 the Russian Federation State Premium for science and technology was awarded to three researchers from LNC for their works on “Imidazoline nitroxides”. The fruitful research activities of Laboratory research fellows allowed them to create from nitroxides a series of high technology products, “a functional spin probes”, the compounds with a set of unique properties which are relevant to various fields of science and technology. These spin probes are designed to monitor local pH values and thiol concentrations, to follow production of nitric oxide NO, formation of superoxide anion radical and other reactive oxygen species. The use of these spin probes allowed LNC in collaboration with researchers from other institutions in Russia and abroad to develop of special methods for analysis and investigation of complex molecular structures, including those related to biological samples on molecular or cellular levels, in isolated organs and tissues. Recently the examples of successful applications of these functional spin probes to noninvasive studies of physiological processes in vivo have been described; the diagnostic procedures are in developmental stage.

Besides that, a broad variety of research is being carried out in LNS currently, including development of new therapeutic agents, new functional materials for applications of organic electronic devices, molecular magnets, mediators of radical polymerization, etc. The range of research activity of LNC is still expanding.

Laboratory of Nitrogen Compounds of NIOCh SB RAS have been renowned in Russia and abroad. The majority of international conferences on EPR biological applications and/or nitroxide chemistry frequently include some scientific contributions by researchers from LNC. The Laboratory of Nitrogen Compounds was the organizer of international conferences on nitroxides in 1989 and in 2005. The LNC is more and more engaged in research collaboration with leading research groups from Russia, USA, Germany, France, Italy, Japan, etc..

Research areas:

Research areas:

The major scientific trends  

• Development of the new methods for synthesis and modification of organic hydroxylamine derivatives (including nitroxides, nitrones, Alkoxyamines, etc.) and a search for the new fields of application of these compounds.
• Molecular design and synthesis of functional spin probes (i.e., those designed to monitor pH, thiols, nitric oxide NO, etc.) for investigation of various complex systems, including biological samples and models, living animals, sorbents, catalysts, etc..
• Molecular design and synthesis of specific spin labels for studies of structure and dynamics of molecular and supramolecular systems, including biological macromolecules and their complexes.
• Molecular design and synthesis of spin traps and spin probes for studies of processes involving short-living free radicals, including biogenic reactive oxygen species.
• The studies of antioxidant properties of nitroxides, hydroxylamines and nitrones; development of the therapeutic agents on the basis of the above mentioned compounds, for prevention and treatment of various pathologies, which origination and/or development is associated with reactive oxygen species; targeting of nitroxide-based antioxidants using natural and/or synthetic biologically active molecules residues.
• Development nitroxide and/or alkoxyamine mediators of free radical polymerization of vinyl monomers.
• Molecular design and synthesis of paramagnetic ligands, paramagnetic liquid crystals and similar nitroxide-containing compounds for preparations of new organic and metalocomplex magnetic materials.
• Development of nitroxide-based materials for microelectronic components, such as organic accumulators, dye-sensitized solar cells, data storage devices, etc..
• Molecular design and synthesis of new 1,1-diphosphonate-based calcium metabolism regulators and cytostatic drugs.

Scientific achievements

 

• The convenient scalable technologies have been developed for preparation of 1,2-hydroxyaminooxymes, 1,2-hydroxyaminoketones, N,N’-bis-hydroxyamines and similar building blocks from easily available chemicals; the utility of these blocks for synthesis of various heterocyclic systems have been demonstrated.
• As a result of extensive studies of reactivities of nitrone and imine moieties in various heterocyclic systems, the original general methods have been developed for chemical modification and synthesis of practically useful compounds.
• The original spin probes, the derivatives of stable nitroxides of imidazoline and imidazolidine series, have been developed, which EPR spectra are highly sensitive to pH changes. Based on these compounds, the methods have been developed for local pH monitoring in microvolumes of heterogeneous samples of various origin (in liposomes, polyelectrolyte pores, membrane surfaces, subcellular fractions and compartments, in extracellular media, in isolated organs and living tissues in vivo), for studies of proton transport, for studies of surface potentials of catalysts, sorbents, membranes, biomacromolecules, etc.The methods have been developed for preparation of imidazoline and/or pyrroline nitroxides with bulky substituents or spirocyclic moieties adjacent to nitroxide group; these nitroxides were shown to be resistant to reduction in biological samples.

 

Collaboration with:

 

• Pacific Institute of Bioorganic Chemistry Far-East Branch of Russian Academy of Science;
• Institute of Bioorganic Chemistry of the National Academy of Sciences of Belarus;
• Buryat State University;
• Institute of Problems of Chemical and Energetic Technologies Siberian Branch of RAS;
• JSC International research and Production holding “Phytochemistry” (Karaganda, Kazakhstan);
• Institute of Chemistry and Chemical Technology Mongolian Academy of Sciences;
• Institute of Organic Chemistry, University of Cologne (Kцln, Germany);
• Laboratory of Molecular Pharmacology, Center for Cancer Research, NCI, USA.

 

The major scientific trends of current researchs/Priority directions

 

• Basic. V.36. “Theoretical chemistry and methodology of oranic synthesis development; new methods of physic-chemical investigations”.
• Interdisciplinary Integration Projects
  • V.37: “Current problems of chemistry of materials, including nanomaterials”.
  • V.41:“Chemical problems of creation of pharmacologically active compounds of new generation”.

 

Current projects

 

• Headed or coordinated by laboratory researchers
  • RAS basic project V.36.6.8:
    • “Development of methods for synthesis of heteroatom-containing organic compounds for biomedical research and for preparation of new materials”. Headed by Prof. Igor A. Grigor’ev.
  • RFBR Projects No.:
    • 11-03-92107-ЯФ_а “Development of novel all-organic liquid crystalline nitroxide radical compounds showing strong magnetic interactions at high temperatures”. Head from RF – Grigor’ev I.A.
    • 12-03-00718-а “Development of specifically targeted nitroxides and hydroxylamines for red-ox status regulation”. Head – Prof. Grigor’ev I.A.
    • 12-03-00737-а “A new synthetic strategy for sterically hindered nitroxides based on intramolecular 1,3-dipolar cycloaddition in alkenyl nitrones”. Head – Dr. Kirilyuk I.A.
    • 12-03-31330 мол_а “Molecular design, synthesis and properties of new redox systems based on nitroxides”. Head – Mostovich E.A.
• Projects or programs in which the Laboratory is engaged
  • Federal research program RF “Physico-chemical studies of functional properties of new nitroxides and of nitroxide-based high-tech materials” headed by Prof Bagryanskaya (application 2012-1.2.1-12-000-1005-020).
  • Moscow city regional scientific programs:
    • “Development and practical application of new methods of healthcare, prophylaxis and diagnostics of cancer, infectious and another dangerous diseases”.
    • “Synthesis and studies of diphosphonic acids as a complexones for calcium metabolism regulation in atherosclerosis plaque”.
  • Interdisciplinary Integration Projects of SB RAS, V.37
    • Project No. 1 “Synthesis of functional nitroxides aimed to create new manetoactive compounds and materials” (Coordinated by corresponding member of RAS Ovcharenko V.I., ITC SB RAS).
    • Project No. 129 “A comprehensive study of soft media condition in electromagnetic field aimed to design highly efficient energy converters of new generation” (Coordinated by Dr Sci Klement’ev V.M., ILP SB RAS).
  • Interdisciplinary Integration Project of SB RAS, V.41
    • Project No. 52 “Oncogenesis of glioma and human brain reparation” (Coordinators: Dr Sci Mordvinov V.A. (ICG SB RAS) and corresponding member of RAS Krivoshapkin A.L. (ICG SB RAS).
  • RFBR Projects No.
    • 10-04-91331-ННИО_а “Nano-electrostatics of biological interfaces”. Head from RF– Academician Skulachev V.P. (MSU).
    • 12-03-01042-а “Novel synthetic methodologies for homo- and co-polymer nanostructured materials”. Head – Dr. Edeleva M.V., ITC SB RAS).
    • 12-04-01435-а “Development and application of new spin probes for in vivo EPR tomography and EPR spectroscopy of spin-labeled proteins”. Head – Bagryanskaya E. G. (NIOCh SB RAS).
   

 

 

 

STAFF

Staff

№	Employee	Position	Room	Phone	Phone in.	email	Publications
							by years
1	Kirilyuk Igor Anatolievich	Lab's Head (Cand. Chem)	207	330-73-87	2-74	This email address is being protected from spambots. You need JavaScript enabled to view it.
2	Dobrynin Sergey Aleksandrovich	Senior Researcher (Cand. Chem.)	207	330-73-87	2-74	This email address is being protected from spambots. You need JavaScript enabled to view it.
3	Mazhukin Dmitry Gennadievich	Senior Researcher (Cand. Chem.)	317 НТК, 231	330-68-52	2-56, 4-10	This email address is being protected from spambots. You need JavaScript enabled to view it.
4	Morozov Denis Aleksandrovich	Senior Researcher (Cand. Chem.)	208	330-73-87	4-11	This email address is being protected from spambots. You need JavaScript enabled to view it.
5	Polienko Yulia Fedorovna	Senior Researcher (Cand. Chem.)	206	330-73-87	4-12	This email address is being protected from spambots. You need JavaScript enabled to view it.
6	Taratayko Andrey Igorevich	Senior Researcher (Cand. Chem.)	231	330-73-87	4-10	This email address is being protected from spambots. You need JavaScript enabled to view it.
7	Zhurko Irina Fridrikhovna	Researcher (Cand. Chem.)	207	330-73-87	2-74	This email address is being protected from spambots. You need JavaScript enabled to view it.
8	Trofimov Dmitry Gennadievich	Leading Engineer	231	330-73-87	4-10	This email address is being protected from spambots. You need JavaScript enabled to view it.
Students
9	Gulman Mark Mikhailovich	laboratory assistant	207	330-73-87	2-74	This email address is being protected from spambots. You need JavaScript enabled to view it.
10	Trakhinina Sofia Yurievna	laboratory assistant	231			This email address is being protected from spambots. You need JavaScript enabled to view it.
11	Usatov Mikhail Sergeevich	laboratory assistant	207			This email address is being protected from spambots. You need JavaScript enabled to view it.
PHD Students
12	Khoroshunova Yulia Vladislavovna	Junior Researcher	208	330-73-87	4-11	This email address is being protected from spambots. You need JavaScript enabled to view it.

PUBLICATIONS

 

Publications over the past years

Laboratory staff publications (DB NIOCh)

Reviews, Articles

2022

1. ACID-CATALYZED PYRIDYLIMIDAZOLINE REARRANGEMENT/ Salnikov G.E., Kirilyuk I.A., Morozov D.A., Cherkasov S.A., Genaev A.M.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 625-639. doi:10.15372/CSD2022426
2. S.A. Dobrynin, M.M. Gulman, D.A. Morozov, I.F. Zhurko, A.I. Taratayko, Yu.S. Sotnikova, Yu.I. Glazachev, Yu.V. Gatilov, I.A. Kirilyuk
   Synthesis of Sterically Shielded Nitroxides Using the Reaction of Nitrones with Alkynylmagnesium Bromides
   Molecules 2022, 27(21), 7626 doi:10.3390/molecules27217626, IF=4.927
3. S.I. Dikalov, A.E. Dikalova, I.A. Kirilyuk
   Coupling of phagocytic NADPH oxidase activity and mitochondrial superoxide production
   Frontiers in Cardiovascular Medicine, 2022, 9, 942736 doi:10.3389/fcvm.2022.942736, IF=5.846
4. S.A. Cherkasov, P.M. Kaletina, Yu.F. Polienko, D. Parkhomenko
   The Kinetic Solvent Effect on 1,3-Dipolar Cycloaddition to 2,2,5,5-Tetramethyl-3-imidazoline-3-oxide-1-oxyl
   ChemPlusChem, V. 87, N 7, July 27, 2022, e202200119 doi:10.1002/cplu.202200119, IF=3.21
5. S. Ketter, M. Dajka, O. Rogozhnikova, S.A. Dobrynin, V.M. Tormyshev, E.G. Bagryanskaya, B. Joseph
   In situ distance measurements in a membrane transporter using maleimide functionalized orthogonal spin labels and 5-pulse electron-electron double resonance spectroscopy
   Journal of Magnetic Resonance Open (companion title to the Journal of Magnetic Resonance), Volumes 10-11, June 2022, 100041 doi:10.1016/j.jmro.2022.100041
6. N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
   Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
   Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
7. A.S. Spitsyna, A.S. Poryvaev, N.E. Sannikova, A.A. Yazikova, I.A. Kirilyuk, S.A. Dobrynin, O.A. Chinak, M.V. Fedin, O.A. Krumkacheva
   Stability of ZIF-8 Nanoparticles in Most Common Cell Culture Media
   Molecules 2022, 27(10), 3240; doi:10.3390/molecules27103240, IF=4.927
8. A.I. Taratayko, Yu.I. Glazachev, I.V. Eltsov, E.I. Chernyak, I.A. Kirilyuk
   3,4-Unsubstituted 2-tert-Butyl-pyrrolidine-1-oxyls with Hydrophilic Functional Groups in the Side Chains
   Molecules 2022, 27(6), 1922 doi:10.3390/molecules27061922, IF=4.411
9. I.O. Timofeev, L.V. Politanskaya, E.V. Tretyakov, Yu.F. Polienko, V.M. Tormyshev, E.G. Bagryanskaya, O.A. Krumkacheva, M.V. Fedin
   Fullerene-based triplet spin labels: methodology aspects for pulsed dipolar EPR spectroscopy
   Phys. Chem. Chem. Phys., 2022, V.24, N 7, Pp. 4475-4484 doi:10.1039/D1CP05545C, IF=3.945
10. L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, N.P. Gritsan, A.A. Dmitriev, M.S. Kazantsev, E.V. Zaytseva, D.A. Parkhomenko, I.V. Beregovaya, G.A. Zakabluk, E.V. Tretyakov
    Multispin Systems with a Rigid Ferrocene-1,1'-diyl-Substituted 1,3-Diazetidine-2,4-diimine Coupler: A General Approach
    European journal of organic Chemistry, V. 2022, N 7, February 18, 2022, e202101234 doi:10.1002/ejoc.202101234, IF=3.261
11. Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025, IF=7.46
12. I.Y. Zhuravleva, A.A. Dokuchaeva, E.V. Karpova, T.P. Timchenko, A.T. Titov, SvS. Shatskaya, Yu.F. Polienko
    Immobilized Bisphosphonates as Potential Inhibitors of Bioprosthetic Calcification: Effects on Various Xenogeneic Cardiovascular Tissues
    Biomedicines 2022, 10(1), 65 doi:10.3390/biomedicines10010065, IF=4.757
13. D.G. Trofimov, Yu.I. Glazachev, A.A. Gorodetsky, D.A. Komarov, T.V. Rybalova, I.A. Kirilyuk
    4-Dialkylamino-2,5-dihydroimidazol-1-oxyls with Functional Groups at the Position 2 and at the Exocyclic Nitrogen: The pH-Sensitive Spin Labels
    Gels 2022, 8(1),11 doi:10.3390/gels8010011, IF=4.432
14. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21

2021

1. A.A. Kuzhelev, D. Dai, V. Denysenkov, I.A. Kirilyuk, E.G. Bagryanskaya, T. F. Prisner
   Influence of Rotational Motion of Nitroxides on Overhauser Dynamic Nuclear Polarization: A Systematic Study at High Magnetic Fields
   The Journal of Physical Chemistry C, 2021, 125, 46, 25651–25659 doi:10.1021/acs.jpcc.1c06979, IF=4.125
2. M.Yu. Ivanov, Yu.F. Polienko, I.A. Kirilyuk, S.A. Prikhod'ko, N
   Peek Inside the Water Mixtures of Ionic Liquids at Molecular Level: Microscopic Properties Probed by EPR Spectroscopy
   Int. J. Mol. Sci. 2021, 22(21), 11900 doi:10.3390/ijms222111900, IF=5.923
3. P. Fehling, K. Buckenmaier, S.A. Dobrynin, D.A. Morozov, Yu.F. Polienko, Yu.V. Khoroshunova, Yu. Borozdina, P. Mayer, J. Engelmann, K. Scheffler, G. Angelovsk, I.A. Kirilyuk
   The effects of nitroxide structure upon 1H Overhauser dynamic nuclear polarization efficacy at ultralow-field
   J. Chem. Phys., 2021, V. 155, N 14, 144203 doi:10.1063/5.0064342, IF=3.487
4. Yu.V. Khoroshunova,D. A. Morozov,A. I. Taratayko,S. A. Dobrynin,I. V. Eltsov,T. V. Rybalova,Yu. S. Sotnikova,D. N. Polovyanenko,N. B. Asanbaeva,I. A. Kirilyuk
   The Reactions of 6-(Hydroxymethyl)-2,2-dimethyl-1-azaspiro[4.4]nonanes with Methanesulfonyl Chloride or PPh3-CBr4
   Molecules 2021, 26(19), 6000 doi:10.3390/molecules26196000, IF=4.411
5. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
   A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
   Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
6. S.A. Dobrynin, M.S. Usatov, I.F. Zhurko, D.A. Morozov, Yu.F. Polienko, Yu.I. Glazachev, D.A. Parkhomenko, M.A. Tyumentsev, Yu.V. Gatilov, E.I. Chernyak, E.G. Bagryanskaya, I.A. Kirilyuk
   A Simple Method of Synthesis of 3-Carboxy-2,2,5,5-Tetraethylpyrrolidine-1-oxyl and Preparation of Reduction-Resistant Spin Labels and Probes of Pyrrolidine Series
   Molecules 2021, 26(19), 5761 doi:10.3390/molecules26195761, IF=4.41
7. S.S. Ovcherenko, O.A. Chinak, A.V. Chechushkov, S.A. Dobrynin, I.A. Kirilyuk, O.A. Krumkacheva, V.A. Richter, E.G. Bagryanskaya
   Uptake of Cell-Penetrating Peptide RL2 by Human Lung Cancer Cells: Monitoring by Electron Paramagnetic Resonance and Confocal Laser Scanning Microscopy
   Molecules 2021, 26(18), 5442 doi:10.3390/molecules26185442, IF=4.41
8. B.Y. Mladenova Kattnig, N.A. Chumakova, D.R. Kattnig, I.A. Grigor’ev, G. Grampp, A.I. Kokorin
   Influence of the Electric Charge of Spin Probes on Their Diffusion in Room-Temperature Ionic Liquids
   The Journal of Physical Chemistry B, 2021, V. 125, N 32, Pp. 9235–9243 doi:10.1021/acs.jpcb.1c02493, IF=2.99
9. D.O. Antonov, D.P. Tambasova, A.B. Shishmakov, I.A. Kirilyuk, E.G. Kovaleva
   Acidic and Electrosurface Properties of Binary TiO2–SiO2 Xerogels Using EPR of pH-Sensitive Nitroxides
   Gels, 2021, 7(3), 119 doi:10.3390/gels7030119, IF=4.702
10. S.A. Cherkasov, A.D. Semikina, P.M. Kaletina, Yu.F. Polienko, D.A. Morozov, A.M. Maksimov, I.A. Kirilyuk, E.G. Bagryanskaya, D. Parkhomenko
    The Kinetics of 1,3-Dipolar Cycloaddition of Vinyl Monomers to 2,2,5,5-Tetramethyl-3-imidazoline-3-oxides
    ChemPhysChem, 2021, V.86, N 8, Pp 1080-1086 doi:10.1002/cplu.202100266, IF=2.862
11. L. N. Grigor’eva,A. Ya. Tikhonov,K. A. Lomanovich,D. G. Mazhukin
    Stable Bicyclic Functionalized Nitroxides: The Synthesis of Derivatives of Aza-nortropinone–5-Methyl-3-oxo-6,8-diazabicyclo[3.2.1]-6-octene 8-oxyls
    Molecules 2021, 26(10), 3050 doi:10.3390/molecules26103050, IF=4.411
12. Yu.F. Polienko, N.M. Kuprikova, D.A. Parkhomenko, Yu.V. Gatilov, E.I. Chernyak, I.A. Kirilyuk
    Synthesis of 2,5-Bis(spirocyclohexane)-Substituted Nitroxides: New Spin Labeling Agents
    Tetrahedron, 2021, V. 81, 131915 doi:10.1016/j.tet.2020.131915, IF=2.457
13. E.V. Zaytseva, D.G. Mazhukin
    Spirocyclic Nitroxides as Versatile Tools in Modern Natural Sciences: From Synthesis to Applications. Part I. Old and New Synthetic Approaches to Spirocyclic Nitroxyl Radicals
    Molecules 2021, 26(3), 677 doi:10.3390/molecules26030677, IF=4.411
14. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158

2020

1. N.A. Chumakova, E.N. Golubeva, S.V. Kuzin, T.A. Ivanova, I.A. Grigoriev, S.V. Kostjuk, M.Ya. Melnikov
   New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
   Polymers 2020, 12(12), 3046 doi:10.3390/polym12123046, IF=3.426
2. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
   Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
   RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
3. S. Cherkasov, D. Parkhomenko, A. Genaev, G. Salnikov, M. Edeleva, D. Morozov, T. Rybalova, I. Kirilyuk, S.R-A. Marque, E. Bagryanskaya
   NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines
   Molecules 2020, 25(21), 5080 doi:10.3390/molecules25215080, IF=3.266
4. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
   Application of EPR to porphyrin-protein agents for photodynamic therapy
   Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
5. S.A. Amitina, E.V. Zaytseva, N.A. Dmitrieva, A.V. Lomanovich, N.V. Kandalintseva, Yu.A. Ten, I.A. Artamonov, A.F. Markov, D.G. Mazhukin
   5-Aryl-2-(3,5-dialkyl-4-hydroxyphenyl)-4,4-dimethyl-4H-imidazole 3-Oxides and Their Redox Species: How Antioxidant Activity of 1-Hydroxy-2,5-dihydro-1H-imidazoles Correlates with the Stability of Hybrid Phenoxyl-Nitroxides
   Molecules 2020, 25(14), 3118 doi:10.3390/molecules25143118, IF=3.267
6. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
   Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
   Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
7. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
   Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
   Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
8. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
   Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
   Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
9. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
   Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
   The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
10. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
11. I.F. Zhurko, S. Dobrynin, A.A. Gorodetskii, Yu.I. Glazachev, T.V. Rybalova, E.I. Chernyak, N. Asanbaeva, E.G. Bagryanskaya, I.A. Kirilyuk
    2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties
    Molecules 2020, 25(4), 845 doi:10.3390/molecules25040845, IF=3.267

2019

1. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
   DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
   Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
2. M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
   Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
   Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
3. V.I. Borovkov, A.I. Taratayko, Yu.N. Molin
   Radiation-Induced Fluorescence from Doped Polyolefins on a Nanosecond Timescale: Kinetics of the Processes Involving Geminate Radical Ions
   The Journal of Physical Chemistry B, Just Accepted ( June 17, 2019) doi:10.1021/acs.jpcb.9b03914, IF=2.923
4. S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
   Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
   Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
5. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
   Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
   Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
6. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
   Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
   Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
7. Yu.V. Khoroshunova, D.A. Morozov, A.I. Taratayko, P.D. Gladkikh, Yu.I. Glazachev, I.A. Kirilyuk
   Synthesis of 1-azaspiro[4.4]nonan-1-oxyls via intramolecular 1,3-dipolar cycloaddition
   Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2036-2042 doi:10.3762/bjoc.15.200, IF=2.595
8. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
   Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
   Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
9. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
   EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
   Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
10. M. Edeleva, D. Morozov, D. Parkhomenko, Yu. Polienko, A. Iurchenkova, I. Kirilyuk, E. Bagryanskaya
    Versatile approach to activation of alkoxyamine homolysis by 1,3-dipolar cycloaddition for efficient and safe nitroxide mediated polymerization
    Chem. Commun., 2019,V. 55, N 2, Pp 190-193 doi:10.1039/C8CC08541B, IF=6.164

2018

1. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
   Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
   J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
2. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
   In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
   Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
3. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
   Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
   Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
4. Yu.A. Ten, O.G. Salnikov, S.A. Amitina, D.V. Stass, T.V. Rybalova, M.S. Kazantsev, A.S. Bogomyakov, E.A. Mostovich, D.G. Mazhukin
   The Suzuki–Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series
   RSC Adv., 2018, V. 8, N 46, Pp 26099-26107 doi:10.1039/C8RA05103H, IF=2.936
5. A.I. Taratayko, T.V. Rybalova, V.A. Reznikov
   Synthesis of paramagnetic spiropyran derivatives
   Chemistry of Heterocyclic Compounds, 2018, V. 54, N 10, pp 981-983 doi:10.1007/s10593-018-2375-y, IF=1.2
6. A. A. Sonina, I.P. Koskin, P.S. Sherin, T. V. Rybalova, I. K. Shundrina, E. A. Mostovich, M. S. Kazantsev
   Crystal packing control of a trifluoromethyl-substituted furan/phenylene co-oligomer
   Acta Crystallographica Section B, 2018, V. 74, N 5, Pp 450-457 doi:10.1107/S2052520618011782, IF=6.467
7. S.A. Dobrynin, Yu.I. Glazachev, Yu.V. Gatilov, E.I. Chernyak, G.E. Salnikov, I.A. Kirilyuk
   Synthesis of 3,4-Bis-(hydroxymethyl)-2,2,5,5-tetraethylpyrrolidin-1-oxyl via 1,3-Dipolar Cycloaddition of Azomethine Ylide to Activated Alkene
   J. Org. Chem., 2018, V. 83, N 10, Pp 5392-5397 doi:10.1021/acs.joc.8b00085, IF=4.805
8. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
   Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
   European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
9. E.V. Zaytseva, Yu.V. Gatilov, D.G. Mazhukin
   The synthesis of new functionalized 1,3,5-triazine-based stable bi- and trinitroxides of the 2,5-dihydroimidazole series
   Arkivoc, 2018, part v, 359-374 doi:10.24820/ark.5550190.p010.614, IF=1.048
10. I.P. Koskin, E.A. Mostovich, E. Benassi, M.S. Kazantsev
    A quantitative topological descriptor for linear co-oligomer fusion
    Chem. Commun., 2018, V. 54, N 52, Pp 7235-7238 doi:10.1039/C8CC03156H, IF=6.29
11. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
12. S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
    Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
    J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
13. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
14. S. Dikalov, Yu.F. Polienko, I. Kirilyuk
    Electron Paramagnetic Resonance Measurements of Reactive Oxygen Species by Cyclic Hydroxylamine Spin Probes
    Antioxidants & Redox Signaling, 2018, V. 28, N 15, Pp 1433-1444 doi:10.1089/ars.2017.7396, IF=6.53
15. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
16. M.S. Kazantsev, A.A. Beloborodova, A.D. Kuimov, I.P. Koskin, E.S. Frantseva, T.V. Rybalova, I.K. Shundrina, C.S. Becker, E.A. Mostovich
    Synthesis, luminescence and charge transport properties of furan/phenylene co-oligomers: The study of conjugation length effect
    Organic Electronics, , 2018, V. 56, May 2018, Pages 208-215 doi:10.1016/j.orgel.2018.01.010, IF=3.68
17. L. Gurskaya, I. Bagryanskaya, E. Amosov, M. Kazantsev, L. Politanskaya, E. Zaytseva, E. Bagryanskaya, A. Chernonosov, E. Tretyakov
    1,3-Diaza[3]ferrocenophanes functionalized with a nitronyl nitroxide group
    Tetrahedron, 2018, V. 74, N 15, Pp 1942-1950 doi:10.1016/j.tet.2018.02.062, IF=2.377
18. V.N. Verkhovlyuk, V.I. Borovkov, V.A. Bagryansky, S.B. Zikirin, A.I. Taratayko, O.A. Anisimov, Yu.N. Molin
    Hyperfine Structure in the OD ESR Spectra of Recombining Charge Pairs in Doped Polyethylene Matrices
    Applied Magnetic Resonance, 2018, V. 49, N 4, pp 345-355 doi:10.1007/s00723-018-0978-1, IF=0.835
19. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
20. Т.С. Фролова, С.Ж. Шарапов, О.И. Синицина, Т.Г. Толстикова, И.А. Григорьев, С.В. Морозов, Ю.В. Юшкова
    Новые ионные конъюгаты на основе a-токоферилсукцината как потенциальные цитотоксические агенты1
    Биоорганическая химия. 2018. Т. 44. № 3. С. 325-332. doi:10.7868/S0132342318030089, IF=0.838
21. S.I. Dikalov, A.E. Dikalova, D.A. Morozov, I.A. Kirilyuk
    Cellular accumulation and antioxidant activity of acetoxymethoxycarbonyl pyrrolidine nitroxides
    Free Radical Research, 2018, V. 52, N 3: International Conference on Electron Paramagnetic Resonance Spectroscopy and Imaging of Biological Systems (EPR-2017), Pp 339-350 doi:10.1080/10715762.2017.1390744, IF=3.038
22. Yu.V. Yushkova, E.I. Chernyak, Yu.V. Gatilov, V.G. Vasil'ev, S.V. Morozov, I.A. Grigor'ev
    Synthesis, Structure, Antioxidant Activity, and Water Solubility of Trolox Ion Conjugates
    Saudi Pharmaceutical Journal, 2018, V. 26, N 1, Pp 84-92 doi:10.1016/j.jsps.2017.10.008, IF=3.11

2017

1. S.A. Popov, L.M. Kornaukhova, A.V. Shpatov, I.A. Grigor'ev
   Synthesis of Conjugates of Ursolic Acid 3-O-Succinate with NO-H₂S Donors
   Chemistry of Natural Compounds, с. 1-3, Article in Press doi: 10.1007/s10600-017-2061-9, IF=0.46
2. И.Ю. Журавлева, М.Б. Васильева, Т.П. Тимченко, Е.В. Кузнецова, Ю.Ф. Полиенко, И.Р. Ничай, И.А. Григорьев, А.В. Богачев-Прокофьев
   Кальцификация эластин-содержащих ксеногенных биоматериалов: влияние консервантов и бисфосфонатов
   Сибирский научный медицинский журнал, 2017, N. 37, № 6, Стр. 28-37 (http://sibmed.net/article.php?lang=rus&id_article=562)
3. L.Bales. Barney, M.M. Bakirov, R.T. Galeev, I.A. Kirilyuk, A.I. Kokorin, K.M. Salikhov
   The Current State of Measuring Bimolecular Spin Exchange Rates by the EPR Spectral Manifestations of the Exchange and Dipole–Dipole Interactions in Dilute Solutions of Nitroxide Free Radicals with Proton Hyperfine Structure
   Applied Magnetic Resonance, 2017, V. 48, N 11-12, pp 1399-1445 doi:10.1007/s00723-017-0958-x, IF=0.864
4. Yu.V. Yushkova, S.V. Morozov, E.I. Chernyak, I.A. Grigor'ev
   Covalent and Ionic Conjugates of Trolox and α-Tocopherol with 1-Aminoadamantane
   Chemistry of Natural Compounds, 2017, V. 53, N 6, Pp 1059-1065 doi:10.1007/s10600-017-2201-2, IF=0.46
5. N.V. Mamontova, E.I. Chernyak, E.V. Amosov, Yu.V. Gatilov, V.I. Vinogradova, S.F. Aripova, S.V. Morozov, I.A. Grigor'ev
   First Ionic Conjugates of Dihydroquercetin Monosuccinate with Amines
   Chemistry of Natural Compounds, 2017, V. 53, N 6, pp 1045-1051 doi:10.1007/s10600-017-2198-6, IF=0.46
6. Yu.V. Yushkova, S.V. Morozov, E.I. Chernyak, N.A. Grigor'ev
   Synthesis of New Trolox-Based Antioxidants Containing Amino-bis-Phosphonic Acids
   Chemistry of Natural Compounds,2017, V. 53, N 4, pp 764-766 doi:10.1007/s10600-017-2115-z, IF=0.46
7. H. Kubota, D.A. Komarov, H. Yasui, S. Matsumoto, O. Inanami, I.A. Kirilyuk, V.V. Khramtsov, H. Hirata
   Feasibility of in vivo three-dimensional T2* mapping using dicarboxy-PROXYL and CW-EPR-based single-point imaging
   Magnetic Resonance Materials in Physics, Biology and Medicine, 2017, V. 30, N 3, pp 291-298 doi:10.1007/s10334-016-0606-8, IF=1.718
8. E.G. Kovaleva, L.S. Molochnikov, D.P. Stepanova, A.V. Pestov, D.G. Trofimov, I.A. Kirilyuk, A.I. Smirnov
   Interfacial Electrostatic Properties of Hydrated Mesoporous and Nanostructured Alumina Powders by Spin Labeling EPR
   Cell Biochemistry and Biophysics, 2017, V. 75, N 2, pp 159-170 doi:10.1007/s12013-016-0767-0, IF=1.32
9. M.A. Voinov, C.T. Scheid, I.A. Kirilyuk, D.G. Trofimov, A.I. Smirnov
   IKMTSL-PTE, a Phospholipid-Based EPR Probe for Surface Electrostatic Potential of Biological Interfaces at Neutral pH: Effects of Temperature and Effective Dielectric Constant of the Solvent
   Journal of Physical Chemistry B, 2017, V. 121, N 11, Pp 2443-2453 doi:10.1021/acs.jpcb.7b00592, IF=3.177
10. V.V. Annenkov, E.N. Danilovtseva, S.S. Khutsishvili, V.A. Pal'shin, Yu.F. Polienko, V.V. Saraev, T.I. Vakul'skaya, S.N. Zelinskiy, I.A. Grigor'ev
    Polyamine-based spin probes for the study of siliceous structures
    Microporous and Mesoporous Materials, 2017, V. 242, Pages 74-81 doi:10.1016/j.micromeso.2017.01.010, IF=3.615
11. A.G. Matveeva, Yu.V. Yushkova, S.V. Morozov, I.A. Grygor'ev, S.A. Dzuba
    Multi-Gaussian Monte Carlo Analysis of PELDOR Data in the Frequency DomainMulti-Gaussian Monte Carlo Analysis of PELDOR Data in the Frequency Domain
    Zeitschrift fur Physikalische Chemie, 2017б V. 231, N 3, Pp 671-688 doi:10.1515/zpch-2016-0830, IF=1.327
12. A.I. Kokorin, B.Y. Mladenova-Kattnig, I.A. Grigor'ev, G. Grampp
    Unexpected Features of the Intramolecular Spin Exchange in Imidazoline Nitroxide Biradicals Dissolved in Ionic Liquids
    Applied Magnetic Resonance, 2017, V. 48, N 3, Pp 287-296 doi:10.1007/s00723-016-0858-5, IF=0.864
13. Organic Hydrogen Sulfide Donor Compounds with Cardioprotective Properties (Review)/ N. I. Tkacheva, S. V. Morozov, B. B. Lomivorotov, I. A. Grigor'ev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 3, pp 165-174 doi:10.1007/s11094-017-1576-5, IF=0.444
14. V. Borovkov, A. Taratayko, A. Bessmertnykh, V. Bagryansky, Yu. Molin
    Solvent Radical Anions in Irradiated Aliphatic Ketones and Esters as Observed Using Time-Resolved Magnetic Field Effects in the Recombination Fluorescence
    Zeitschrift fur Physikalische Chemie, 2017,V. 231, N 2, Pp. 311-323 doi:10.1515/zpch-2016-0818, IF=1.327
15. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, И.А. Григорьев, Н.И. Ткачева, В.И. Родионов
    Оценка эффективности действия нового местного гемостатического ванкомицин-содержащего средства на основе окисленной целлюлозы в эксперименте
    Сиб. мед. журнал.-2017. - Т. 32, № 1. - С. 108-111.
16. I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
    A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
    Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
17. А.М. Чернявский, И.А. Григорьев, С.В. Морозов, А.Р. Таркова
    Первый российский комплексный гемостатик
    Наука из первых рук. 2017. Т. 73. № 1. С. 84-89.

2016

1. А.Р. Таркова, С.В. Морозов, Н.И. Ткачева, В.И. Родионов, И.А. Григорьев, А.М. Чернявский
   Оценка гемостатических свойств нового местного антибиотик-содержащего средства на основе окисленной целлюлозы в эксперименте
   Сибирский научный медицинский журнал, 2016, т.36, № 6, 12-17
2. Yu.V. Yushkova, S.V. Morozov, Chernyak, I.A. Grigor'ev
   Synthesis of Ionic Biologically Active Conjugates from Trolox and α-Tocopherol Succinates
   Chemistry of Natural Compounds, 2016, V. 52, N 6, pp 1015-1019 doi:10.1007/s10600-016-1850-x, IF=0.472
3. O.D. Zakharova, T.S. Frolova, Yu.V. Yushkova, E.I. Chernyak, A.G. Pokrovsky, M.A. Pokrovsky, S.V. Morozov, O.I. Sinitsina, I.A. Grigor'ev, G.A. Nevinsky
   Antioxidant and antitumor activity of trolox, trolox succinate, an α-tocopheryl succinate conjugates with nitroxides
   European Journal of Medicinal Chemistry, 2016, V. 122, Pages 127-137 doi:10.1016/j.ejmech.2016.05.051, IF=3.901
4. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin
   Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series
   Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049, IF=5.77
5. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
   Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
   Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
6. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, Н.И. Ткачева, И.А. Григорьев, В.И. Родионов
   Экспериментальная оценка гемостатической активности нового антибиотик-содержащего средства местного действия на основе окисленной целлюлозы
   Современная медицина: актуальные вопросы. 2016. № 8 (50). С. 19-26.
7. A.A. Gorodetsky, I.A. Kirilyuk, V.V. Khramtsov, D.A. Komarov
   Functional electron paramagnetic resonance imaging of ischemic rat heart: Monitoring of tissue oxygenation and pH
   Magnetic Resonance in Medicine, 2016,V. 76, N 1, Pp 350-358 doi:10.1002/mrm.25867, IF=3.782
8. Yu.F. Polienko, O.A. Snytnikova, V.V. Yanshole, E.I. Chernyak, S.V. Morozov, I.A. Grigor'ev, Yu.P. Tsentalovich
   Effect of the spacer length and nitroxide sterical shielding upon photostability of spin-labeled kynurenines
   Journal of Photochemistry and Photobiology A: Chemistry, V.322-323, 15 May-1 June 2016, Pp 76-84 doi:10.1016/j.jphotochem.2016.03.007, IF=2.476
9. А.М. Чернявский, А.Р. Таркова, Т.М. Рузматов, С.В. Морозов, И.А. Григорьев
   Инфекции в кардиохирургии
   Хирургия. Журнал им. Н.И. Пирогова. 2016. № 5. С. 64-68.
10. A.A. Kuzhelev, R.K. Strizhakov, O.A. Krumkacheva, Y.F. Polienko, D.A. Morozov, G.Yu. Shevelev, D.V. Pyshnyi, I.A. Kirilyuk, M.V. Fedin, E.G. Bagryanskaya
    Room-Temperature Electron Spin Relaxation of Nitroxides Immobilized in Trehalose: Effect of Substituents Adjacent to NO-group
    Journal of Magnetic Resonance, V. 266, May 2016, Pages 1-7 doi:10.1016/j.jmr.2016.02.014, IF=2.888
11. S.A. Popov, L.M. Kornaukhova, A.V. Shpatov, I.A. Grigor'ev
    Synthesis of Ursolic Acid Conjugates Containing a Furoxan Moiety
    Chemistry of Natural Compounds, 2016, V. 52, N 3, pp 555-557 doi:10.1007/s10600-016-1708-2, IF=0.472
12. K. Suzuki, Y. Takemoto, S. Takaoka, K.Taguchi. Y. Uchida, D.G. Mazhukin, I.A. Grigor'ev, R. Tamura
    Chiral all-organic nitroxide biradical liquid crystals showing remarkably large positive magneto-LC effects
    Chem. Commun., 2016,52(20), 3935-3938 doi:10.1039/C5CC09202G, IF=6.566
13. S.A. Popov, L.M. Kornaukhova, A.V. Shpatov, I.A. Grigorev
    Synthesis of Conjugate Esters of 5-(4-Hydroxyphenyl)-3H-1,2-Dithiole-3-Thione and Ursolic Acid 3-O-ACYL Derivatives
    Chemistry of Natural Compounds, 2016, V. 52, N 1, pp 183-185 doi:10.1007/s10600-016-1588-5, IF=0.472

2015

1. I. A. Kirilyuk, A. A. Bobko, S. V. Semenov, D. A. Komarov, I. G. Irtegova, I. A. Grigor'ev, E. G. Bagryanskaya
   The effect of sterical shielding on the redox properties of imidazoline and imidazolidine nitroxides
   J. Org. Chem., 2015, 80 (18), pp 9118-9125 doi:10.1021/acs.joc.5b01494, IF=4.721
2. M. Kozuleva, I. Klenina, I. Mysin, I. Kirilyuk, V. Opanasenko, I. Proskuryakov, B. Ivanov
   Quantification of superoxide radical production in thylakoid membrane using cyclic hydroxylamines
   Free Radical Biology and Medicine, V. 89, 2015, Pp 1014-1023 doi:10.1016/j.freeradbiomed.2015.08.016, IF=5.736
3. Efficacy of different forms of local hemostatic materials based on oxidize cellulose in the experiment/ A.R. Tarkova, A.M. Chernyavskiy, I.A. Grigor'ev, S.V. Morozov, V.I. Rodionov, N.I. Kravchenko// Вестник хирургии им. И.И. Грекова, 2015, Т. 174. № 6. С. 56-59.(in Russian)
4. Yu.V. Yushkova, E.I. Chernyak, S.V. Morozov, I.A. Grigor'ev
   Antioxidants Based on Covalently and Ionically Bound Trolox Conjugates
   Chemistry of Natural Compounds, November 2015, V. 51, N 6, pp 1070-1073 doi:10.1007/s10600-015-1494-2, IF=0.509
5. K.S. Taletskiy, V.I. Borovkov, L.N. Schegoleva, I.V. Beregovaya, A.I. Taratayko, Y.N. Molin
   Radical Cationic Pathway for the Decay of Ionized Glyme Molecules in Liquid Solution
   Journal of Physical Chemistry B, 2015, V. 119, N 45, Pages 14472-14478 doi:10.1021/acs.jpcb.5b06086, IF=3.302
6. А.Р. Таркова, А.М. Чернявский, И.А. Григорьев, С.В. Морозов, В.И. Родионов
   Исследование местных гемостатических средств с целью профилактики осложнений срединной стернотомии в эксперименте
   В сборнике: Современные аспекты диагностики и лечения в кардиохирургии Материалы научно-практической конференции с международным участием. 2015. С. 78-80.
7. Studies of Carbomer Gels Using Rotational Viscometry and Spin Probes/ A. N. Lyapunov, E. P. Bezuglaya, N. A. Lyapunov, I. A. Kirilyuk// Pharmaceutical Chemistry Journal, 2015, V. 49, N 9, pp 639-644 doi:10.1007/s11094-015-1344-3, IF=0.451
8. C. Becker, N. Chukanov, I. Grigor’ev
   New amino-bisphosphonate building blocks in the synthesis of bisphosphonic derivatives based on lead compounds
   Phosphorus, Sulfur, and Silicon and the Related Elements, 2015, V. 190, N 7, 1201-1212. 10.1080/10426507.2014.979989 doi:10.1080/10426507.2014.979989, IF=0.561
9. T.S. Frolova, O.D. Zakharova, Y.F. Polienko, Y.V. Yushkova, E.I. Chernyak, S.V. Morozov, O.I. Sinitsina, I.A. Grigor’ev, G.A. Nevinsky
   Conjugates of trolox and alpha-tocopheryl succinate with nitroxides: Synthesis, antioxidant and antitumor activity
   International Journal of Medicine and Pharmaceutical Sciences. 2015. Vol. 5. No. 3. P. 9-24.
10. A.E. Dikalova, I.A. Kirilyuk, S.I. Dikalov
    Antihypertensive effect of mitochondria-targeted proxyl nitroxides
    Redox Biology, V. 4, 2015, Pp 355-362 doi:10.1016/j.redox.2014.12.012
11. Local hemostatic agent based on oxidized cellulose/ A.R. Tarkova, A.M. Chernyavskiy, S.V. Morozov, I.A. Grigor’ev, N.I. Tkacheva, V.I. Rodionov// The Siberian Scientific Medical Journal, 2015, V. 35, № 2, Pp 11-15
12. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigoriev
    Electrical potential near hydrated surface of ordered mesoporous molecular sieves assessed by EPR of molecular pH-probes
    Microporous and Mesoporous Materials, Volume 203, February 2015, Pages 1-7 doi:10.1016/j.micromeso.2014.10.010, IF=3.453
13. About the mechanism of membrane permeability enhancement by substances in their intermolecular complexes with polysaccharide arabinogalactan from larches Larix sibirica and Larix gmelinii/ A. V. Dushkin, Yu. S. Chistyachenko, D. A. Komarov, M. V. Khvostov, T. G. Tolstikova, I. F. Zhurko, I. A. Kirilyuk, I. A. Grigor’ev, N. Z. Lyakhov// Doklady Biochemistry and Biophysics, January 2015, Volume 460, Issue 1, pp 9-12 doi:10.1134/S1607672915010020, IF=0.343
14. S.A. Popov, A.V. Shpatov, I.A. Grigor’ev
    Synthesis of Substituted Esters of Ursolic, Betulonic, and Betulinic Acids Containing the Nitroxyl Radical 4-Amino-2,2,6,6-Tetramethylpiperidine-1-Oxyl
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 87-90 doi:10.1007/s10600-015-1209-8, IF=0.509
15. Sh.N. Zhurakulov, V.A. Babkin, E.I. Chernyak, S.V. Morozov, I.A. Grigor’ev, M.G. Levkovich, V.I. Vinogradova
    Aminomethylation of 1-Aryl-6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinolines by Dihydroquercetin
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 57-61 doi:10.1007/s10600-015-1203-1, IF=0.509

2014

1. X-ray emission and X-ray photoelectron study of the electronic structure of paramagnetic and diamagnetic derivatives of 3-imidazoline/ L. N. Mazalov, A. D. Fedorenko, N. A. Kryuchkova, Yu. P. Dikov, Yu. F. Polienko, I. A. Grigor'ev// Journal of Structural Chemistry, November 2014, Volume 55, Issue 6, pp 1044-1056 doi:10.1134/S0022476614060079, IF=0.5
2. Первые спин-меченые сукцинильные производные α-токоферола и тролокса/ Ю.В. Юшкова, Е.И. Черняк, С.В. Морозов, И.А. Григорьев// Химия природных соединений. 2014, № 5, С. 718-722 doi:10.1007/s10600-014-1093-7, IF=0.5
3. E.V. Zaytseva, A.V. Shernyukov, A.M. Genaev, R. Tamura, I.A. Grigor’ev, D.G. Mazhukin
   New spirocyclic nitroxides of 2,5-dihydroimidazole series flanked by two mesogenic fragments
   ARKIVOC, 2014, (vi) 10-24. http://www.arkat-usa.org/get-file/51547/ doi:10.3998/ark.5550190.p008.808, IF=1.75
4. L.A. Shundrin, I.A. Kirilyuk, I.A. Grigor'ev
   3-Carboxy-2,2,5,5-tetra(²H₃)methyl-[4-²H(¹H)]-3-pyrroline-(1-¹⁵N)-1-oxyl as a spin probe for in vivo L-band electron paramagnetic resonance imaging
   Mendeleev Communications, V. 24, N 5, September–October 2014, Pp 298-300. doi:10.1016/j.mencom.2014.09.017, IF=1.154
5. Local hemostasis control by using of oxidized cellulose drugs/ A.M. Cherniavskii, I.A. Grigor'ev, S.V. Morozov, A.R. Tarkova, N.I. Tkacheva// Хирургия. Журнал им. Н.И. Пирогова. 2014. № 8. С. 71-75
6. I.A. Grigor'ev, N.I. Tkacheva, S.V. Morozov
   Conjugates of Natural Compounds with Nitroxyl Radicals as a Basis for Creation of Pharmacological Agents of New Generation
   Current Medicinal Chemistry, 2014, 21(24), pp 2839-2852. doi:10.2174/0929867321666140304153104, IF=3.714
7. Синтез диастереомерных спироциклических нитроксильных радикалов ряда 3-имидазолина с двумя мезогенными группами/ Е.В.Зайцева, А.В.Шернюков, С.А.Амитина, Р.Тамура, И.А.Григорьев// Хим.Гетероцикл.Соедин., 2014, N 8, 1207-1220. doi:10.1007/s10593-014-1571-7, IF=0.698
8. Синтез первых конъюгатов флавоноида дигидрокверцетина в алкалоидом цитизином/ Н.В. Кошелева, Е.И. Черняк, С.В. Морозов, В.И. Виноградова, Ш.Ш. Сагдуллаев, Н.Д. Абдуллаев, И.А. Григорьев// Химия природных соединений, 2014, № 3, С.383-385 doi:10.1007/s10600-014-0982-0, IF=0.5
9. Synthesis and study of antitumor activity of tetraethyl 2-(2',2',6',6'-Tetramethylpiperidin-4'-ylamino)ethylidene-1,1-bisphosphonate/ I. A. Grigor’ev, D. A. Morozov, V. A. Svyatchenko, N. N. Kiselev, V. B. Loktev, E. A. Luk’yanets, G. N. Vorozhtsov// Doklady Chemistry, July 2014, V. 457, N 1, pp 137-140. doi:10.1134/S0012500814070064, IF=0.351
10. Effect of the surface charge on the complexing and catalytic properties of Сu²⁺-containing composite materials based on zirconia and powdered cellulose/ E. G. Kovaleva, L. S. Molochnikov, E. V. Parshina, A. B. Shishmakov, Yu. V. Mikushina, I. A. Kirilyuk, I. A. Grigor’ev// Russian Journal of Physical Chemistry B, 2014, V. 8, N 3, pp 317-325. doi:10.1134/S199079311403021X, IF=0.335
11. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
12. Использование реакции Манниха для синтеза спин-меченых производных природного флаваноида дигидрокверцетина/ Н.В. Кошелева, Е.И. Черняк, Ю.Ф. Полиенко, С.В. Морозов, И.А. Григорьев// Химия природных соединений, 2014, № 2, С. 231-235 doi:10.1007/s10600-014-0927-7, IF=0.5
13. M.V. Edeleva, D.A. Parkhomenko, D.A. Morozov, S.A. Dobrynin, D.G. Trofimov, B. Kanagatov, I.A. Kirilyuk, E.G. Bagryanskaya
    Controlled/living polymerization of methyl methacrylate using new sterically hindered imidazoline nitroxides prepared via intramolecular 1,3-dipolar cycloaddition reaction
    Journal of Polymer Science Part A: Polymer Chemistry, 2014, V. 52, N 7, pp 929-943. doi:10.1002/pola.27071, IF=3.244
14. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
15. Spirocyclic 2,5-dihydro-1H-imidazole 1-oxyl radicals with a mesogenic substituent on C⁴. Synthesis and crystal structure/ E. V. Zaytseva, Yu. V. Gatilov, S. A. Amitina, R. Tamura, I. A. Grigor’ev, D. G. Mazhukin// Russian Journal of Organic Chemistry, 2014, V. 50, N 1, pp 72-77. doi:10.1134/S107042801401014X, IF=0.675

2013

1. Hepatoprotective Activity of Betulonic Acid Amides Containing Piperidine or Pyrrolidine Nitroxide Moieties/ I. V. Sorokina, D. S. Baev, N. A. Zhukova, T. G. Tolstikova, A. N. Antimonova, N. I. Petrenko, E. E. Shults, and I. A. Grigor’ev// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 6, pp. 668–670. doi:10.1134/S1068162013060083, IF=0.523
2. A. I. Taratayko, C.S. Becker,.I. A. Grigor’ev,Y. V. Gatilov, T. V. Rybalova, V. A. Reznikov
   Synthesis of 3,4-dihydro-2H-pyrrole 1-oxide based aldonitrones as potential spin trapping agents
   Arkivoc 2013, (iv), 272-290.full text doi:10.3998/ark.5550190.p008.159, IF=1.57
3. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigor'ev
   Dynamics of pH-sensitive nitroxide radicals in water adsorbed in ordered mesoporous molecular sieves by EPR Spectroscopy
   Microporous and Mesoporous Materials, 2013, V. 179, P. 258-264. doi:10.1016/j.micromeso.2013.05.019, IF=3.365
4. K.S. Bekker, N.V. Chukanov, I.A. Grigor'ev
   Synthesis of a bis-Phosphonic Acid Derivative of Trolox, a New Potential Antioxidant
   Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 785-786. doi:10.1007/s10600-013-0746-2, IF=0.598
5. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, V.A. Svyatchenko, N.N. Kiselev, V.B. Loktev, I.A. Grigor’ev
   First bis-Phosphonic Acid Derivatives of the Plant Alkaloid Cytisine
   Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 781-782. doi:10.1007/s10600-013-0744-4, IF=0.598
6. R. Nazarewicz, A. Dikalova, A. Bikineyeva, S. Ivanov, I.A. Kirilyuk, I.A. Grigor'ev, S.I. Dikalov
   Does Scavenging of Mitochondrial Superoxide Attenuate Cancer Prosurvival Signaling Pathways?
   Antioxidants & Redox Signaling, 2013, V.19, N 4, pp 344-349. doi:10.1089/ars.2013.5185, IF=7.189
7. Modification of Cellulose as a Promising Direction in the Design of New Materials/ N. I. Tkacheva, S. V. Morozov, I. A. Grigor’ev, D. M. Mognonov, N. A. Kolchanov// Polymer Science Series B, 2013, V. 55, N 7-8, pp 409-429. doi:10.1134/S1560090413070063, IF=0.439
8. K.S. Bekker, N.V. Chukanov, S.A. Popov, I.A. Grigor'ev
   Conjugates of Bisphosphonates with Derivatives of Ursolic, Betulonic, and Betulinic Acids
   Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 581-582. doi:10.1007/s10600-013-0680-3, IF=0.598
9. K.S. Bekker, N.V. Chukanov, I.A. Grigor'ev
   Synthesis of a bisphosphonate derivative of folic acid
   Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 495-495. doi:10.1007/s10600-013-0646-5, IF=0.598
10. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, Yu.V. Gatilov, I.A. Grigor'ev
    First spin-labeled cytisine derivatives
    Chemistry of Natural Compounds, 2013, V. 49, N 2, P. 311-315. doi:10.1007/s10600-013-0588-y, IF=0.598
11. Yu.V. Yushkova, E.I. Chernyak, Yu.F. Polienko, Yu.V. Gatilov, S.V. Morozov, I.A. Grigor’ev
    Synthesis of spin-labeled amides of 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (trolox)
    Chemistry of Natural Compounds, 2013, V. 49, N 2, P. 253-257. doi:10.1007/s10600-013-0574-4, IF=0.598
12. Synthetic transformations of higher triterpenoids. XXX. Synthesis and cytotoxic activity of betulonic acid amides with fragments of nitroxyl radicals/ A. N. Antimonova, N. I. Petrenko, E. E. Shults, Yu. F. Polienko, M. M. Shakirov, I. G. Irtegova, M. A. Pokrovskii, K. M. Sherman, I. A. Grigor’ev, A. G. Pokrovskii, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 181-185 doi:10.1134/S1068162013020027, IF=0.523