| 1 | Popov S.A.
    ,        Shults E.E.
    ,        Shpatov A.V.
    ,        Semenova M.D. Synthesis of ursane-derived regioisomeric 2-amino-1,3,4-oxadiazoles and 3-thioxo-1,2,4-triazoles
 Chemistry of Heterocyclic Compounds. 2024.
        V.60.     N7-8.     P.377-389. DOI: 10.1007/s10593-024-03350-y
            WOS
        
            Scopus
        
            OpenAlex
 | 
                    
                                                        | 2 | 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
 | 
                    
                                                        | 3 | 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
 | 
                    
                                                        | 4 | 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 | 
                    
                                                        | 5 | 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
 | 
                    
                                                        | 6 | Borisova M.S.
    ,        Yarovaya O.I.
    ,        Semenova M.D.
    ,        Tolstikova T.G.
    ,        Salakhutdinov N.F. Antiulcerogenic activity of borneol derivatives
 Russian Chemical Bulletin. 2018.
        V.67.     N3.     P.558-561. DOI: 10.1007/s11172-018-2110-y
            WOS
        
            Scopus
        
            РИНЦ
        
            OpenAlex
 | 
                    
                                                        | 7 | Борисова М.С.
    ,        Яровая О.И.
    ,        Семенова М.Д.
    ,        Толстикова Т.Г.
    ,        Салахутдинов Н.Ф. Противоязвенная активность производных борнеола
 Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2018.
            №3.     С.558-561. 
            РИНЦ
 | 
                    
                                                        | 8 | Sokolova A.S.
    ,        Yarovaya O.I.
    ,        Semenova M.D.
    ,        Shtro A.A.
    ,        Orshanskaya I.R.
    ,        Zarubaev V.V.
    ,        Salakhutdinov N.F. Synthesis and in vitro study of novel borneol derivatives as potent inhibitors of the influenza A virus
 
  MedChemComm. 2017.
        V.8.     N5.     P.960-963. DOI: 10.1039/c6md00657d
            WOS
        
            Scopus
        
            РИНЦ
        
            OpenAlex |