Articles - Sciact

Articles (93)

#	Публикация
1	Qi Z. , Xie P. , Wang Z. , Zhou H. , Tao R. , Popov S.A. , Yang G. , Shults E.E. , Wang C. Synthesis of novel ursolic acid-gallate hybrids via 1,2,3-triazole linkage and its anti-oxidant and anti-inflammatory activity study Arabian Journal of Chemistry. 2024. 105762 :1-27. DOI: 10.1016/j.arabjc.2024.105762
2	Popov S.A. , Qi Z. , Wang C. , Shults E.E. Synthesis of ursane-derived isothiocyanates and study of their reactions with series of amines and ammonia Journal of Sulfur Chemistry. 2023. V.44. N5. P.523-541. DOI: 10.1080/17415993.2023.2193669 WOS РИНЦ
3	Khalikova D. , An’kov S. , Zhukova N. , Tolstikova T. , Popov S. , Saiko A. Effect of the Composition of Leuzea and Cranberry Meal Extracts on Metabolic Processes in Norm and Pathology Pharmaceuticals. 2023. V.16. N5. 768 :1-13. DOI: 10.3390/ph16050768 WOS Scopus РИНЦ
4	Shpatov A.V. , Zakharova S.S. , Popov S.A. Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles Chemistry of Natural Compounds. 2022. V.58. N2. P.290-296. DOI: 10.1007/s10600-022-03662-5 WOS РИНЦ
5	Qi Z. , Yang G. , Deng T. , Wang J. , Zhou H. , Popov S.A. , Shults E.E. , Wang C. Design and linkage optimization of ursane-thalidomide-based PROTACs and identification of their targeted-degradation properties to MDM2 protein Bioorganic Chemistry. 2021. V.111. 104901 . DOI: 10.1016/j.bioorg.2021.104901 WOS Scopus РИНЦ
6	Popov S.A. , Wang C. , Qi Z. , Shults E.E. , Turks M. Synthesis of water-soluble ester-linked ursolic acid–gallic acid hybrids with various hydrolytic stabilities Synthetic Communications. 2021. V.51. N16. P.2466-2477. DOI: 10.1080/00397911.2021.1939057 WOS Scopus РИНЦ
7	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
8	Luginina J. , Linden M. , Bazulis M. , Kumpins V. , Mishnev A. , Popov S.A. , Golubeva T.S. , Waldvogel Siegfried R. S.R. , Shults E.E. , Turks M. Electrosynthesis of Stable Betulin-Derived Nitrile Oxides and their Application in Synthesis of Cytostatic Lupane-Type Triterpenoid-Isoxazole Conjugates European Journal of Organic Chemistry. 2021. V.2021. N17. P.2557-2577. DOI: 10.1002/ejoc.202100293 WOS Scopus РИНЦ
9	Pyatrikas D.V. , Gorbyleva E.L. , Fedyaeva A.V. , Zakharova S.S. , Shpatov A.V. , Popov S.A. , Borovskii G.B. Search for biologically active substances of natural origin based on low-polar conifer extracts Известия вузов. Прикладная химия и биотехнология. 2020. V.10. N2. P.240-250. DOI: 10.21285/2227-2925-2020-10-2-240-250 WOS РИНЦ
10	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
11	Shpatov A.V. , Frolova T.S. , Popov S.A. , Sinitsyna O.I. , Salnikova O.I. , Zheng G. , Yan L. , Sinelnikova N.V. , Pshennikova L.M. , Kochetov A.V. Lipophilic Metabolites from Five-Needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity Chemistry and Biodiversity. 2020. V.17. N8. e2000201 . DOI: 10.1002/cbdv.202000201 WOS Scopus
12	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
13	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
14	Толстикова Т.Г. , Сорокина И.В. , Жукова Н.А. , Морозова Е.А. , Харитонов Ю.В. , Миронов М.Е. , Попов С.А. , Шульц Э.Э. Доступные метаболиты растений сибири как источники инновационных препаратов для медицины ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2018. Т.26. №3. С.329-344. DOI: 10.15372/KhUR20180308 РИНЦ
15	Grazhdannikov A.E. , Kornaukhova L.M. , Rodionov V.I. , Pankrushina N.A. , Shults E.E. , Fabiano-Tixier A.S. , Popov S.A. , Chemat F. Selecting a Green Strategy on Extraction of Birch Bark and Isolation of Pure Betulin Using Monoterpenes ACS Sustainable Chemistry and Engineering. 2018. V.6. N5. P.6281-6288. DOI: 10.1021/acssuschemeng.8b00086 WOS Scopus РИНЦ
16	Popov S.A. , Kornaukhova L.M. , Shpatov A.V. , Grigore'ev I.A. Synthesis of Conjugates of Ursolic Acid 3-O-Succinate with NO-H2S Donors Chemistry of Natural Compounds. 2017. V.53. N3. P.592-594. DOI: 10.1007/s10600-017-2061-9 WOS Scopus РИНЦ
17	Popov S.A. , Sheremet O.P. , Kornaukhova L.M. , Grazhdannikov A.E. , Shults E.E. 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. P.122-132. DOI: 10.1016/j.indcrop.2017.03.020 WOS Scopus РИНЦ
18	Shpatov A.V. , Popov S.A. , Salnikova O.I. , Kukina T.P. , Shmidt E.N. , Um B.H. Composition and Bioactivity of Lipophilic Metabolites from Needles and Twigs of Korean and Siberian Pines (Pinus koraiensis Siebold & Zucc. and Pinus sibirica Du Tour) Chemistry and Biodiversity. 2017. V.14. N2. e1600203 . DOI: 10.1002/cbdv.201600203 WOS Scopus РИНЦ
19	Popov S.A. , Kornaukhova L.M. , Shpatov A.V. , Grigor'ev I.A. Synthesis of Ursolic Acid Conjugates Containing a Furoxan Moiety Chemistry of Natural Compounds. 2016. V.52. N3. P.555-557. DOI: 10.1007/s10600-016-1708-2 WOS Scopus РИНЦ
20	Popov S.A. , Kozlova L.P. , Kornaukhova L.M. , Shpatov A.V. Simple and efficient process for large scale preparation of betulonic acid from birch bark extracts Industrial Crops and Products. 2016. V.92. P.197-200. DOI: 10.1016/j.indcrop.2016.07.026 WOS Scopus РИНЦ

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