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Baev Dmitrii Sergeevich

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Articles - 55 , Conference theses - 1


Articles (55) More info

1 Yarovaya O.I. , Filimonov A.S. , Baev D.S. , Borisevich S.S. , Zaykovskaya A.V. , Chirkova V.Y. , Marenina M.K. , Meshkova Y.V. , Belenkaya S.V. , Shcherbakov D.N. , Gureev M.A. , Luzina O.A. , Pyankov O.V. , Salakhutdinov N.F. , Khvostov M.V.
The Potential of Usnic-Acid-Based Thiazolo-Thiophenes as Inhibitors of the Main Protease of SARS-CoV-2 Viruses
Viruses. 2024. V.16. N2. P.215. DOI: 10.3390/v16020215 WOS Scopus OpenAlex
2 Yarovaya O.I. , Baev D.S. , Kovaleva K.S. , Gatilov Y.V. , Meshkova Y.V. , Marinina M.K. , Oreshko V.V. , Tolstikova T.G. , Salakhutdinov N.F.
Synthesis and Properties of New Conjugates of Isatin and Bicyclic Monoterpenes
Russian Journal of General Chemistry. 2024. V.94. N1. P.81-92. DOI: 10.1134/s1070363224010080 WOS Scopus OpenAlex
3 Shchegravina E.S. , Usova S.D. , Baev D.S. , Mozhaitsev E.S. , Shcherbakov D.N. , Belenkaya S.V. , Volosnikova E.A. , Chirkova V.Y. , Sharlaeva E.A. , Svirshchevskaya E.V. , Fonareva I.P. , Sitdikova A.R. , Salakhutdinov N.F. , Yarovaya O.I. , Fedorov A.Y.
Synthesis of conjugates of (aR,7S)-colchicine with monoterpenoids and investigation of their biological activity
Russian Chemical Bulletin. 2023. V.72. N1. P.248-262. DOI: 10.1007/s11172-023-3730-4 WOS Scopus РИНЦ OpenAlex
4 Baev D.S. , Blokhin M.E. , Chirkova V.Y. , Belenkaya S.V. , Luzina O.A. , Yarovaya O.I. , Salakhutdinov N.F. , Shcherbakov D.N.
Triterpenic Acid Amides as Potential Inhibitors of the SARS-CoV-2 Main Protease
Molecules. 2023. V.28. N1. P.303. DOI: 10.3390/molecules28010303 WOS Scopus РИНЦ OpenAlex
5 Sokolova A.S. , Baranova D.V. , Yarovaya O.I. , Zybkina A.V. , Mordvinova E.D. , Zaykovskaya A.V. , Baev D.S. , Tolstikova T.G. , Shcherbakov D.N. , Pyankov O.V. , Maksyutov R.A. , Salakhutdinov N.F.
Synthesis of (1S)-(+)-camphor-10-sulfonamides and evaluation of their anti-filovirus activity
Russian Chemical Bulletin. 2023. V.72. N10. P.2536-2547. DOI: 10.1007/s11172-023-4056-y WOS Scopus РИНЦ OpenAlex
6 Meshkova Y.V. , Baev D.S. , Sorokina I.V. , Popadyuk I.I. , Salomatina O.V. , Zhukova N.A. , Tolstikova T.G. , Salakhutdinov N.F.
Experimental Evaluation of 3-meta-Pyridine-1,2,4-Oxadiazole Derivative of Deoxycholic Acid as a Prototype of 5-α-Reductase Inhibitors in In Silico and In Vivo Models
Russian Journal of Bioorganic Chemistry. 2023. V.49. N1. P.52-64. DOI: 10.1134/s1068162023010181 WOS Scopus РИНЦ OpenAlex
7 Dalinger A.I. , Baev D.S. , Yarovaya O.I. , Chirkova V.Y. , Sharlaeva E.A. , Belenkaya S.V. , Shcherbakov D.N. , Salakhutdinov N.F. , Vatsadze S.Z.
Synthesis of non-symmetric N-benzylbispidinol amides and study of their inhibitory activity against the main protease of the SARS-CoV-2 virus
Russian Chemical Bulletin. 2023. V.72. N1. P.239-247. DOI: 10.1007/s11172-023-3729-x WOS Scopus РИНЦ OpenAlex
8 Filimonov A.S. , Yarovaya O.I. , Zaykovskaya A.V. , Rudometova N.B. , Shcherbakov D.N. , Chirkova V.Y. , Baev D.S. , Borisevich S.S. , Luzina O.A. , Pyankov O.V. , Maksyutov R.A. , Salakhutdinov N.F.
(+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
Viruses. 2022. V.14. N10. 2154 :1-21. DOI: 10.3390/v14102154 WOS Scopus РИНЦ OpenAlex
9 Reshetnikov D.V. , Ivanov I.D. , Baev D.S. , Rybalova T.V. , Mozhaitsev E.S. , Patrushev S.S. , Vavilin V.A. , Tolstikova T.G. , Shults E.E.
Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
Molecules. 2022. V.27. N24. P.8787. DOI: 10.3390/molecules27248787 WOS РИНЦ OpenAlex
10 Sorokina I.V. , Zhukova N.A. , Meshkova Y.V. , Baev D.S. , Tolstikova T.G. , Bakarev M.A. , Lushnikova E.L.
Modeling of Benign Prostatic Hyperplasia in Rats with a High Dose of Testosterone
Bulletin of Experimental Biology and Medicine. 2022. V.173. N5. P.680-686. DOI: 10.1007/s10517-022-05613-0 WOS РИНЦ OpenAlex
11 Khusnutdinova E.F. , Petrova A.V. , Lobov A.N. , Kukovinets O.S. , Baev D.S. , Kazakova O.B.
Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
Natural Product Research. 2021. V.35. N21. P.3850-3858. DOI: 10.1080/14786419.2020.1744139 WOS Scopus OpenAlex
12 Fomenko V. , Blokhin M. , Kuranov S. , Khvostov M. , Baev D. , Borisova M.S. , Luzina O. , Tolstikova T.G. , Salakhutdinov N.F.
Triterpenic Acid Amides as a Promising Agent for Treatment of Metabolic Syndrome
Scientia Pharmaceutica. 2021. V.89. N1. 4 :1-14. DOI: 10.3390/scipharm89010004 WOS Scopus РИНЦ OpenAlex
13 Gromova M.A. , Kharitonov Y.V. , Borisov S.A. , Baev D.S. , Tolstikova T.G. , Shul’ts E.E.
Synthetic Transformations of Higher Terpenoids. 39.∗ Synthesis and Analgesic Activity of Isopimaric Acid Derivatives
Chemistry of Natural Compounds. 2021. V.57. P.474–481. DOI: 10.1007/s10600-021-03391-1 WOS Scopus РИНЦ OpenAlex
14 Sirazhetdinova N.S. , Savelyev V.A. , Baev D.S. , Golubeva T.S. , Klimenko L.S. , Tolstikova T.G. , Ganbaatar J. , Shults E.E.
Synthesis, characterization and anticancer evaluation of nitrogen-substituted 1-(3-aminoprop-1-ynyl)-4-hydroxyanthraquinone derivatives
Medicinal Chemistry Research. 2021. V.30. P.1541–1556. DOI: 10.1007/s00044-021-02754-1 WOS Scopus РИНЦ OpenAlex
15 Kazakova O. , Tret’yakova E. , Baev D.
Evaluation of A-azepano-triterpenoids and related derivatives as antimicrobial and antiviral agents
Journal of Antibiotics. 2021. V.74. P.559–573. DOI: 10.1038/s41429-021-00448-9 WOS Scopus OpenAlex
16 Semenova M.D. , Popov S.A. , Golubeva T.S. , Baev D.S. , Shults E.E. , Turks M.
Synthesis and Cytotoxicity of Sulfanyl, Sulfinyl and Sulfonyl Group Containing Ursane Conjugates with 1,3,4-Oxadiazoles and 1,2,4-Triazoles
ChemistrySelect. 2021. V.6. N25. P.6472-6477. DOI: 10.1002/slct.202101594 WOS Scopus РИНЦ OpenAlex
17 Finke A.O. , Ravaeva M.Y. , Krasnov V.I. , Cheretaev I.V. , Chuyan E.N. , Baev D.S. , Shults E.E.
Cross-Coupling-Cyclocondensation Reaction Sequence to Access a Library of Ring-C Bridged Pyrimidino-tetrahydrothebaines and Pyrimidinotetrahydrooripavines
ChemistrySelect. 2021. V.6. N29. P.7391-7397. DOI: 10.1002/slct.202101790 WOS Scopus OpenAlex
18 Patrushev S.S. , Burova L.G. , Shtro A.A. , Rybalova T.V. , Baev D.S. , Shirokikh I.V. , Evstropov A.N. , Shults E.E.
Modifications of isoalantolactone leading to effective anti-bacterial and anti-viral compounds
Letters in Drug Design and Discovery. 2021. V.18. N7. P.686-700. DOI: 10.2174/1570180817999201211193151 WOS Scopus РИНЦ OpenAlex
19 Sirazhetdinova N.S. , Savelyev V.A. , Frolova T.S. , Baev D.S. , Klimenko L.S. , Chernikov I.V. , Oleshko O.S. , Sarojan T.A. , Pokrovskii A.G. , Shults E.E.
1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
Molecules. 2020. V.25. N11. 2547 . DOI: 10.3390/molecules25112547 WOS Scopus OpenAlex
20 Popov S.A. , Semenova M.D. , Baev D.S. , Frolova T.S. , Shults E.E. , Wang C. , Turks M.
Synthesis of cytotoxic urs-12-ene- and 28-norurs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles
Steroids. 2020. V.153. 108524 . DOI: 10.1016/j.steroids.2019.108524 WOS Scopus РИНЦ OpenAlex
21 Popov S.A. , Semenova M.D. , Baev D.S. , Frolova T.S. , Shestopalov M.A. , Wang C. , Qi Z. , Shults E.E. , Turks M.
Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
Steroids. 2020. V.162. 108698 . DOI: 10.1016/j.steroids.2020.108698 WOS Scopus РИНЦ OpenAlex
22 Sokolova A.S. , Yarovaya O.I. , Zybkina A.V. , Mordvinova E.D. , Shcherbakova N.S. , Zaykovskaya A.V. , Baev D.S. , Tolstikova T.G. , Shcherbakov D.N. , Pyankov O.V. , Maksyutov R.A. , Salakhutdinov N.F.
Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
European Journal of Medicinal Chemistry. 2020. V.207. 112726 . DOI: 10.1016/j.ejmech.2020.112726 WOS Scopus РИНЦ OpenAlex
23 Khlebnicova T.S. , Piven Y.A. , Lakhvich F.A. , Sorokina I.V. , Frolova T.S. , Baev D.S. , Tolstikova T.G.
Betulinic acid-azaprostanoid hybrids: Synthesis and pharmacological evaluation as anti-inflammatory agents
Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry. 2020. V.19. N3. P.254-267. DOI: 10.2174/1871523018666190426152049 Scopus РИНЦ OpenAlex
24 Kuranov S. , Luzina O. , Khvostov M. , Baev D. , Kuznetsova D. , Zhukova N. , Vassiliev P. , Kochetkov A. , Tolstikova T. , Salakhutdinov N.
Bornyl derivatives of p-(Benzyloxy)phenylpropionic acid: In vivo evaluation of antidiabetic activity
Pharmaceuticals. 2020. V.13. N11. 404 :1-22. DOI: 10.3390/ph13110404 WOS Scopus РИНЦ OpenAlex
25 Cheremnykh K.P. , Savelyev V.A. , Borisov S.A. , Ivanov I.D. , Baev D.S. , Tolstikova T.G. , Vavilin V.A. , Shults E.E.
Hybrides of Alkaloid Lappaconitine with Pyrimidine Motif on the Anthranilic Acid Moiety: Design, Synthesis, and Investigation of Antinociceptive Potency
Molecules. 2020. V.25. N23. 5578; . DOI: 10.3390/molecules25235578 WOS Scopus РИНЦ OpenAlex
26 Prima D.O. , Makarov A.G. , Bagryanskaya I.Y. , Kolesnikov A.E. , Zargarova L.V. , Baev D.S. , Eliseeva T.F. , Politanskaya L.V. , Makarov A.Y. , Slizhov Y.G. , Zibarev A.V.
Fluorine-Containing n-6 and Angular and Linear n-6-n' (n, n'=5, 6, 7) Diaza-Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way
ChemistrySelect. 2019. V.4. N8. P.2383-2386. DOI: 10.1002/slct.201803970 WOS Scopus РИНЦ OpenAlex
27 Cheremnykh K.P. , Savelyev V.A. , Pokrovskii M.A. , Baev D.S. , Tolstikova T.G. , Pokrovskii A.G. , Shults E.E.
Design, synthesis, cytotoxicity, and molecular modeling study of 2,4,6-trisubstituted pyrimidines with anthranilate ester moiety
Medicinal Chemistry Research. 2019. V.28. N4. P.545-558. DOI: 10.1007/s00044-019-02314-8 WOS Scopus РИНЦ OpenAlex
28 Frolova T.S. , Lipeeva A.V. , Baev D.S. , Baiborodin S.I. , Orishchenko K.E. , Kochetov A.V. , Sinitsyna O.I.
Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
Bioorganic Chemistry. 2019. V.87. P.876-887. DOI: 10.1016/j.bioorg.2018.11.052 WOS Scopus РИНЦ OpenAlex
29 Sokolova A.S. , Baranova D.V. , Yarovaya O.I. , Baev D.S. , Polezhaeva O.A. , Zybkina A.V. , Shcherbakov D.N. , Tolstikova T.G. , Salakhutdinov N.F.
Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections
Russian Chemical Bulletin. 2019. V.68. N5. P.1041-1046. DOI: 10.1007/s11172-019-2517-0 WOS Scopus РИНЦ OpenAlex
30 Lipeeva A.V. , Zakharov D.O. , Burova L.G. , Frolova T.S. , Baev D.S. , Shirokikh I.V. , Evstropov A.N. , Sinitsyna O.I. , Tolsikova T.G. , Shults E.E.
Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
Molecules. 2019. V.24. N11. 2126 . DOI: 10.3390/molecules24112126 WOS Scopus РИНЦ OpenAlex
31 Khomenko T.M. , Korchagina D.V. , Baev D.S. , Vassiliev P.M. , Volcho K.P. , Salakhutdinov N.F.
Antimicrobial Activity of Substituted Benzopentathiepin-6-amines
Journal of Antibiotics. 2019. V.72. N8. P.590-599. DOI: 10.1038/s41429-019-0191-y WOS Scopus РИНЦ OpenAlex
32 Popov S.A. , Semenova M.D. , Baev D.S. , Sorokina I.V. , Zhukova N.A. , Frolova T.S. , Tolstikova T.G. , Shults E.E. , Turks M.
Lupane-type conjugates with aminoacids, 1,3,4-oxadiazole and 1,2,5-oxadiazole-2-oxide derivatives: Synthesis, anti-inflammatory activity and in silico evaluation of target affinity
Steroids. 2019. V.150. 108443 . DOI: 10.1016/j.steroids.2019.108443 WOS Scopus РИНЦ OpenAlex
33 Kremis S.A. , Baev D.S. , Lipeeva A.V. , Shults E.E. , Tolstikova T.G. , Sinitsyna O.I. , Kochetov A.V. , Frolova T.S.
Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
Journal of Biochemical and Molecular Toxicology. 2019. V.33. N11. e22396 . DOI: 10.1002/jbt.22396 WOS Scopus РИНЦ OpenAlex
34 Zakharova O. , Nevinsky G. , Politanskaya L. , Baev D. , Ovchinnikova L. , Tretyakov E.
Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
Journal of Fluorine Chemistry. 2019. V.226. UNSP 109353 . DOI: 10.1016/j.jfluchem.2019.109353 WOS Scopus РИНЦ OpenAlex
35 Kong R. , Zhu X. , Meteleva E.S. , Polyakov N.E. , Khvostov M.V. , Baev D.S. , Tolstikova T.G. , Dushkin A.V. , Su W.
Atorvastatin calcium inclusion complexation with polysaccharide arabinogalactan and saponin disodium glycyrrhizate for increasing of solubility and bioavailability
Drug Delivery and Translational Research. 2018. V.8. N5. P.1200-1213. DOI: 10.1007/s13346-018-0565-x WOS Scopus РИНЦ OpenAlex
36 Frolova T.S. , Lipeeva A.V. , Baev D.S. , Tsepilov Y.A. , Sinitsyna O.I.
Apoptosis as the basic mechanism of cytotoxic action of ursolic and pomolic acids in glioma cells
Molecular Biology. 2017. V.51. N5. P.705-711. DOI: 10.1134/S0026893317050090 WOS Scopus РИНЦ OpenAlex
37 Sokolova A.S. , Yarovaya O.I. , Baev D.S. , Shernyukov A.V. , Shtro A.A. , Zarubaev V.V. , Salakhutdinov N.F.
Aliphatic and alicyclic camphor imines as effective inhibitors of influenza virus H1N1
European Journal of Medicinal Chemistry. 2017. V.127. P.661-670. DOI: 10.1016/j.ejmech.2016.10.035 WOS Scopus РИНЦ OpenAlex
38 Lipeeva A.V. , Baev D.S. , Dolgikh M.P. , Tolstikova T.G. , Shults E.E.
Rapid Access to Oxazine Fused Furocoumarins and in vivo and in silico Studies of theirs Biological Activity
Medicinal Chemistry. 2017. V.13. N7. P.625-632. DOI: 10.2174/1573406413666170601114527 WOS Scopus РИНЦ OpenAlex
39 Kong R. , Zhu X. , Meteleva E.S. , Chistyachenko Y.S. , Suntsova L.P. , Polyakov N.E. , Khvostov M.V. , Baev D.S. , Tolstikova T.G. , Yu J. , Dushkin A.V. , Su W.
Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
International Journal of Pharmaceutics. 2017. V.534. N1-2. P.108-118. DOI: 10.1016/j.ijpharm.2017.10.011 WOS Scopus РИНЦ OpenAlex
40 Zhivetyeva S.I. , Zakharova O.D. , Ovchinnikova L.P. , Baev D.S. , Bagryanskaya I.Y. , Shteingarts V.D. , Tolstikova T.G. , Nevinsky G.A. , Tretyakov E.V.
Phosphonium betaines derived from hexafluoro-1,4-naphthoquinone: Synthesis and cytotoxic and antioxidant activities
Journal of Fluorine Chemistry. 2016. V.192. P.68-77. DOI: 10.1016/j.jfluchem.2016.10.014 WOS Scopus РИНЦ OpenAlex
41 Lipeeva A.V. , Khvostov M.V. , Baev D.S. , Shakirov M.M. , Tolstikova T.G. , Shults E.E.
Synthesis, in vivo Anticoagulant Evaluation and Molecular Docking Studies of Bicoumarins Obtained from Furocoumarin Peucedanin
Medicinal Chemistry. 2016. V.12. N7. P.674-683. DOI: 10.2174/1573406412666160129105115 WOS Scopus РИНЦ OpenAlex
42 D'yakonov V.A. , Dzhemileva L.U. , Makarov A.A. , Mulyukova A.R. , Baev D.S. , Khusnutdinova E.K. , Tolstikova T.G. , Dzhemilev U.M.
nZ,(n+4) Z-Dienoic fatty acids: a new method for the synthesis and inhibitory action on topoisomerase I and II alpha
Medicinal Chemistry Research. 2016. V.25. N1. P.30-39. DOI: 10.1007/s00044-015-1446-1 WOS Scopus РИНЦ OpenAlex
43 Maksimova G.A. , Pakharukova M.Y. , Kashina E.V. , Zhukova N.A. , Lvova M.N. , Khvostov M.V. , Baev D.S. , Katokhin A.V. , Tolstikova T.G. , Mordvinov V.A.
The morphofunctional and biochemical characteristics of opisthorchiasis-associated cholangiocarcinoma in a Syrian hamster model
Russian Journal of Genetics: Applied Research. 2016. V.6. N4. P.454-462. DOI: 10.1134/S2079059716040134 Scopus РИНЦ OpenAlex
44 Govdi A.I. , Sorokina I.V. , Baev D.S. , Bryzgalov A.O. , Tolstikova T.G. , Tolstikov G.A. , Vasilevsky S.F.
Acetylenic derivatives of betulonic acid amide as a new type of compounds possessing spasmolytic activity
Russian Chemical Bulletin. 2015. V.64. N6. P.1327-1334. DOI: 10.1007/s11172-015-1013-4 WOS Scopus РИНЦ OpenAlex
45 Nechepurenko I.V. , Boyarskikh U.A. , Khvostov M.V. , Baev D.S. , Komarova N.I. , Filipenko M.L. , Tolstikova T.G. , Salakhutdinov N.F.
Hypolipidemic Berberine Derivatives with a Reduced Aromatic Ring C
Chemistry of Natural Compounds. 2015. V.51. N5. P.916-922. DOI: 10.1007/s10600-015-1447-9 WOS Scopus РИНЦ OpenAlex
46 Lipeeva A.V. , Pokrovsky M.A. , Baev D.S. , Shakirov M.M. , Bagryanskaya I.Y. , Tolstikova T.G. , Pokrovsky A.G. , Shults E.E.
Synthesis of 1H-1,2,3-triazole linked aryl(arylamidomethyl) - dihydrofurocoumarin hybrids and analysis of their cytotoxicity
European Journal of Medicinal Chemistry. 2015. V.100. P.119-128. DOI: 10.1016/j.ejmech.2015.05.016 WOS Scopus OpenAlex
47 D'yakonov V.A. , Dzhemileva L.U. , Makarov A.A. , Mulukova A.R. , Baev D.S. , Khusnutdinova E.K. , Tolstikova T.G. , Dzhemilev U.M.
Stereoselective synthesis of 11-phenylundeca-5Z,9Z-dienoic acid and investigation of its human topoisomerase I and II alpha inhibitory activity
Bioorganic and Medicinal Chemistry Letters. 2015. V.25. N11. P.2405-2408. DOI: 10.1016/j.bmcl.2015.04.011 WOS Scopus РИНЦ OpenAlex
48 D'yakonov V.A. , Dzhemileva L.U. , Makarov A.A. , Mulyukova A.R. , Baev D.S. , Khusnutdinova E.K. , Tolstikova T.G. , Dzhemilev U.M.
11-Phenylundeca-5Z,9Z-dienoic Acid: Stereoselective Synthesis and Dual Topoisomerase I/II alpha Inhibition
Current Cancer Drug Targets. 2015. V.15. N6. P.504-510. DOI: 10.2174/1568009615666150506093155 WOS Scopus РИНЦ OpenAlex
49 Govdi A.I. , Sokolova N.V. , Sorokina I.V. , Baev D.S. , Tolstikova T.G. , Mamatyuk V.I. , Fadeev D.S. , Vasilevsky S.F. , Nenajdenko V.G.
Synthesis of new betulinic acid-peptide conjugates and in vivo and in silico studies of the influence of peptide moieties on the triterpenoid core activity
MedChemComm. 2015. V.6. N1. P.230-238. DOI: 10.1039/c4md00236a WOS Scopus РИНЦ OpenAlex
50 Semenov D.E. , Zhukova N.A. , Ivanova E.P. , Sorokina I.V. , Baiev D.S. , Nepomnyashchikh G.I. , Tolstikova T.G. , Biryukova M.S.
Hepatoprotective Properties of Betulonic Acid Amide and Heptral in Toxic Liver Injury Induced by Carbon Tetrachloride in Combination with Ethanol
Bulletin of Experimental Biology and Medicine. 2015. V.158. N3. P.336-341. DOI: 10.1007/s10517-015-2756-5 WOS Scopus РИНЦ OpenAlex

Conference theses (1) More info

1 Prima D.O. , Baev D.S. , Vorontsova E.V. , Frolova T.S. , Bagryanskaya I.Y. , Slizhov Y.G. , Tolstikova T.G. , Makarov A.Y. , Zibarev A.V.
New Cancer Cells Apoptosis Agents: Fluorinated Aza-Heterocycles
AIP Conference Proceedings. 2017. V.1882. 020057 . DOI: 10.1063/1.5001636 WOS Scopus РИНЦ OpenAlex

Identifiers

ResearcherID: L-4273-2013
Scopus ID: 56479229200 , 55203191400
ORCID: 0000-0002-1795-9256
Elibrary ID: 534178