Kazakova OB - Search Results

1

Structural modifications of 2,3-indolobetulinic acid: Design and synthesis of highly potent α-glucosidase inhibitors.

Khusnutdinova EF, Petrova AV, Thu HNT, Tu ALT, Thanh TN, Thi CB, Babkov DA, Kazakova OB. Khusnutdinova EF, et al. Among authors: kazakova ob. Bioorg Chem. 2019 Jul;88:102957. doi: 10.1016/j.bioorg.2019.102957. Epub 2019 Apr 29. Bioorg Chem. 2019. PMID: 31077913

2

Betulin and ursolic acid synthetic derivatives as inhibitors of Papilloma virus.

Kazakova OB, Giniyatullina GV, Yamansarov EY, Tolstikov GA. Kazakova OB, et al. Bioorg Med Chem Lett. 2010 Jul 15;20(14):4088-90. doi: 10.1016/j.bmcl.2010.05.083. Epub 2010 May 25. Bioorg Med Chem Lett. 2010. PMID: 20558062

3

[Synthesis of new olean-18(19)-ene derivatives from allobetulin].

Kazakova OB, Khusnutdinova ÉF, Tolstikov GA, Suponitskiĭ KIu. Kazakova OB, et al. Bioorg Khim. 2010 Jul-Aug;36(4):552-5. doi: 10.1134/s1068162010040102. Bioorg Khim. 2010. PMID: 20823924 Russian.

4

[Synthesis and cytotoxicity of allobetulin derivatives].

Kazakova OB, Smirnova IE, Khusnutdinova EF, Zhukova OS, Fetisova LV, Apryshko GN, Medvedeva NI, Iamansarov EIu, Baĭkova IP, Nguen TT, Thu do T. Kazakova OB, et al. Bioorg Khim. 2014 Sep-Oct;40(5):608-17. doi: 10.1134/s1068162014050082. Bioorg Khim. 2014. PMID: 25895356 Russian.

5

Inhibition of Alpha-Glucosidase by Synthetic Derivatives of Lupane, Oleanane, Ursane and Dammarane Triterpenoids.

Khusnutdinova EF, Smirnova IE, Giniyatullina GV, Medvedeva NI, Yamansarov EY, Kazakov DV, Kazakova OB, Linh PT, Viet do Q, Huong DT. Khusnutdinova EF, et al. Among authors: kazakova ob. Nat Prod Commun. 2016 Jan;11(1):33-5. Nat Prod Commun. 2016. PMID: 26996014

6

Synthesis and antimalarial activity of 3'-trifluoromethylated 1,2,4-trioxolanes and 1,2,4,5-tetraoxane based on deoxycholic acid.

Yamansarov EY, Kazakov DV, Medvedeva NI, Khusnutdinova EF, Kazakova OB, Legostaeva YV, Ishmuratov GY, Huong LM, Ha TTH, Huong DT, Suponitsky KY. Yamansarov EY, et al. Among authors: kazakova ob. Steroids. 2018 Jan;129:17-23. doi: 10.1016/j.steroids.2017.11.008. Epub 2017 Nov 24. Steroids. 2018. PMID: 29180289

7

Synthesis and antimycobacterial activity of triterpeni≿ A-ring azepanes.

Medvedeva NI, Kazakova OB, Lopatina TV, Smirnova IE, Giniyatullina GV, Baikova IP, Kataev VE. Medvedeva NI, et al. Among authors: kazakova ob. Eur J Med Chem. 2018 Jan 1;143:464-472. doi: 10.1016/j.ejmech.2017.11.035. Epub 2017 Nov 21. Eur J Med Chem. 2018. PMID: 29202408

8

Synthesis of A-ring quinolones, nine-membered oxolactams and spiroindoles by oxidative transformations of 2,3-indolotriterpenoids.

Khusnutdinova EF, Kazakova OB, Lobov AN, Kukovinets OS, Suponitsky KY, Meyers CB, Prichard MN. Khusnutdinova EF, et al. Among authors: kazakova ob. Org Biomol Chem. 2019 Jan 16;17(3):585-597. doi: 10.1039/c8ob02624f. Org Biomol Chem. 2019. PMID: 30574983

9

Diastereoselective Synthesis of Triterpenoid 1,2,4-Trioxolanes by Griesbaum Co-ozonolysis.

Kazakova OB, Khusnutdinova EF, Petrova AV, Yamansarov EY, Lobov AN, Fedorova AA, Suponitsky KY. Kazakova OB, et al. J Nat Prod. 2019 Sep 27;82(9):2550-2558. doi: 10.1021/acs.jnatprod.9b00393. Epub 2019 Sep 6. J Nat Prod. 2019. PMID: 31490689

10

Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity.

Khusnutdinova EF, Petrova AV, Lobov AN, Kukovinets OS, Baev DS, Kazakova OB. Khusnutdinova EF, et al. Among authors: kazakova ob. Nat Prod Res. 2021 Nov;35(21):3850-3858. doi: 10.1080/14786419.2020.1744139. Epub 2020 Mar 28. Nat Prod Res. 2021. PMID: 32223360

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