Поздразделение:
Лаборатория медицинской химии (ЛМХ)
Руководитель:
зав. лабораторией (дхн) Шульц Эльвира Эдуардовна
Публикации (по IF ) сотрудников подразделения (БД НИОХ СО РАН)
- A.E. Grazhdannikov, L.M. Kornaukhova, V.I. Rodionov, N.A. Pankrushina, E.E. Shults, A.S. Fabiano-Tixier, S.A. Popov, F. Chemat
Selecting a green strategy on extraction of birch bark and isolation of pure betulin using monoterpenes
ACS Sustainable Chem. Eng., , 2018, 6 (5), pp 6281-6288 doi:10.1021/acssuschemeng.8b00086, IF=6.14
- E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
- Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
Bioorganic Chemistry, Volume 111, June 2021, 104901 doi:10.1016/j.bioorg.2021.104901, IF=5.275
- D.V. Reshetnikov, I.D. Ivanov, D.S. Baev, T.V. Rybalova, E.S. Mozhaitsev, S.S. Patrushev, V.A. Vavilin, T.G. Tolstikova, E.E. Shults
Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
Molecules 2022, 27(24), 8787 doi:10.3390/molecules27248787, IF=4.927
- Yu.V. Kharitonov, E.E. Shults
An Approach toward 17-Arylsubstituted Marginatafuran-Type Isospongian Diterpenoids via a Palladium-Catalyzed Heck–Suzuki Cascade Reaction of 16-Bromolambertianic Acid
Molecules 2022, 27(9), 2643 doi:10.3390/molecules27092643, IF=4.927
- M.E. Mironov, S.A. Borisov, T.V. Rybalova, D.S. Baev, T.G. Tolstikova, E.E. Shults
Synthesis of Anti-Inflammatory Spirostene-Pyrazole Conjugates by a Consecutive Multicomponent Reaction of Diosgenin with Oxalyl Chloride, Arylalkynes and Hydrazines or Hydrazones
Molecules 2022, 27(1), 162 doi:10.3390/molecules27010162, IF=4.927
- E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
- M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
- T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
- V.A. Stepanova, S.S. Patrushev, T.V. Rybalova, E.E. Shults
Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent
Journal of Molecular Structure, V.1247, 5 January 2022, 131373 doi:10.1016/j.molstruc.2021.131373, IF=3.841
- S.F. Vasilevsky, A.I. Govdi, E.E. Shults, M.M. Shakirov, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, I.V. Alabugin
Efficient synthesis of the first betulonic acid -acetylene hybrids and their hepatoprotective and anti-inflammatory activity
Bioorg. Med. Chem. 2009, V. 17, N 14, 5164-5169. doi:0.1016/j.bmc.2009.05.059, IF=3.75
- B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
- M.A. Timoshenko, Yu.V. Kharitonov, M.M. Shakirov, I.Yu. Bagryanskaya, E.E. Shults
Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives
ChemistryOPEN, V. 5, N 1, pp 65-70, February 2016 doi:10.1002/open.201500187, IF=3.585
- A.V. Lipeeva, M.A. Pokrovsky, D.S. Baev, M.M. Shakirov, I.Y. Bagryanskaya, T.G. Tolstikova, A.G. Pokrovsky, E.E. Shults
Synthesis of 1H-1,2,3-triazole linked aryl(arylamidomethyl) - dihydrofurocoumarin hybrids and analysis of their cytotoxicity
European Journal of Medicinal Chemistry, V.100, 2015, Pp 119-128 doi:10.1016/j.ejmech.2015.05.016, IF=3.447
- K.P. Cheremnykh, V.A. Savelyev, E.E. Shults
An Efficient Access to 3,5-Disubstituted Isoxazoles with Anthranilate Ester Moiety: Alkaloid Lappaconitine – Aryl Conjugates with an Isoxazole Linker
Asian Journal of Organic Chemistry, V. 10, N 10, Pp. 2638-2643 doi:10.1002/ajoc.202100474, IF=3.319
- N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
- K.P. Cheremnykh, V.A. Savelyev, S.A. Borisov, I.D. Ivanov, D.S. Baev, T.G. Tolstikova, V.A. Vavilin, E.E. Shults
Hybrides of Alkaloid Lappaconitine with Pyrimidine Motif on the Anthranilic Acid Moiety: Design, Synthesis, and Investigation of Antinociceptive Potency
Molecules 2020, 25(23), 5578 doi:10.3390/molecules25235578, IF=3.266
- A.A. Ivanov, E.A. Ukladov, S.A. Kremis, S.Z. Sharapov, S.I. Baiborodin, A.V. Lipeeva, E.E. Shults, T.S. Golubeva
Investigation of cytotoxic and antioxidative activity of 1,2,3-triazolyl-modified furocoumarins and 2,3-dihydrofurocoumarins
Protoplasma , 2022, 259 (5), Pp. 1321-1330 doi:10.1007/s00709-022-01739-0, IF=3.186
- S.A. Popov, O.P. Sheremet, L.M. Kornaukhova, A.E. Grazhdannikov, E.E. Shults
An approach to effective green extraction of triterpenoids from outer birch bark using ethyl acetate with extractant recycle
Industrial Crops and Products, 2017, V.102, Pp 122-132 doi:10.1016/j.indcrop.2017.03.020, IF=3.18
- A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06
