1
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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
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2
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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
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3
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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
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4
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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
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РИНЦ
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5
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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
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6
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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
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7
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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
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