Smirnova I - Search Results

1

Synthesis and cholinesterase inhibiting potential of A-ring azepano- and 3-amino-3,4-seco-triterpenoids.

Kazakova O, Smirnova I, Lopatina T, Giniyatullina G, Petrova A, Khusnutdinova E, Csuk R, Serbian I, Loesche A. Kazakova O, et al. Among authors: smirnova i. Bioorg Chem. 2020 Aug;101:104001. doi: 10.1016/j.bioorg.2020.104001. Epub 2020 Jun 10. Bioorg Chem. 2020. PMID: 32683137

2

[Synthesis and anti-inflammatory activity of quinopimaric acid derivatives].

Kazakova OB, Tret'iakova EV, Smirnova IE, Spirikhin LV, Tolstikov GA, Chudov EV, Bazekin GV, Ismagilova AF. Kazakova OB, et al. Among authors: smirnova ie. Bioorg Khim. 2010 Mar-Apr;36(2):277-82. doi: 10.1134/s1068162010020160. Bioorg Khim. 2010. PMID: 20531487 Russian.

3

An efficient oxyfunctionalization of quinopimaric acid derivatives with ozone.

Kazakova OB, Tretyakova EV, Smirnova IE, Nazyrov TI, Kukovinets OS, Tolstikov GA, Suponitskii KY. Kazakova OB, et al. Among authors: smirnova ie. Nat Prod Commun. 2013 Mar;8(3):293-6. Nat Prod Commun. 2013. PMID: 23678794

4

Synthesis and anticancer activity of quinopimaric and maleopimaric acids’ derivatives.

Tretyakova EV, Smirnova IE, Kazakova OB, Tolstikov GA, Yavorskaya NP, Golubeva IS, Pugacheva RB, Apryshko GN, Poroikov VV. Tretyakova EV, et al. Bioorg Med Chem. 2014 Nov 15;22(22):6481-9. doi: 10.1016/j.bmc.2014.09.030. Bioorg Med Chem. 2014. PMID: 25440729

5

One-pot synthesis of hollongdione from dipterocarpol.

Smirnova IE, Kazakova OB, Huong do TT, Minnibaeva EM, Lobov AN, Suponitsky KY. Smirnova IE, et al. Nat Prod Commun. 2014 Oct;9(10):1417-20. Nat Prod Commun. 2014. PMID: 25522528

6

[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. Among authors: smirnova ie. Bioorg Khim. 2014 Sep-Oct;40(5):608-17. doi: 10.1134/s1068162014050082. Bioorg Khim. 2014. PMID: 25895356 Russian.

7

Synthesis and antiviral activity of maleopimaric and quinopimaric acids' derivatives.

Tretyakova EV, Smirnova IE, Salimova EV, Odinokov VN. Tretyakova EV, et al. Bioorg Med Chem. 2015 Oct 15;23(20):6543-50. doi: 10.1016/j.bmc.2015.09.006. Epub 2015 Sep 5. Bioorg Med Chem. 2015. PMID: 26372075 Review.

8

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: smirnova ie. Nat Prod Commun. 2016 Jan;11(1):33-5. Nat Prod Commun. 2016. PMID: 26996014

9

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: smirnova ie. 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

10

The Introduction of Hydrazone, Hydrazide, or Azepane Moieties to the Triterpenoid Core Enhances an Activity Against M. tuberculosis.

Kazakova OB, Medvedeva NI, Smirnova IE, Lopatina TV, Veselovsky AV. Kazakova OB, et al. Among authors: smirnova ie. Med Chem. 2021;17(2):134-145. doi: 10.2174/1573406416666200115161700. Med Chem. 2021. PMID: 31939731

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