Petrova A - 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: petrova a. Bioorg Chem. 2020 Aug;101:104001. doi: 10.1016/j.bioorg.2020.104001. Epub 2020 Jun 10. Bioorg Chem. 2020. PMID: 32683137

2

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: petrova av. Bioorg Chem. 2019 Jul;88:102957. doi: 10.1016/j.bioorg.2019.102957. Epub 2019 Apr 29. Bioorg Chem. 2019. PMID: 31077913

3

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. Among authors: petrova av. 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

4

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: petrova av. 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

5

Allobetulone rearrangement to l8αH,19βH-ursane triterpenoids with antiviral activity.

Babaev M, Khusnutdinova E, Lobov A, Galimova Z, Petrova A, Rybalova T, Nguyen HTT, Meyers C, Prichard M, Kazakova O. Babaev M, et al. Among authors: petrova a. Nat Prod Res. 2022 Jul;36(13):3286-3296. doi: 10.1080/14786419.2020.1855159. Epub 2020 Dec 8. Nat Prod Res. 2022. PMID: 33287588

6

Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis.

Kazakova O, Rubanik L, Lobov A, Poleshchuk N, Baikova I, Kapustina Y, Petrova A, Korzun T, Lopatina T, Fedorova A, Rybalova T, Polovianenko D, Mioc M, Șoica C. Kazakova O, et al. Among authors: petrova a. Steroids. 2021 Nov;175:108912. doi: 10.1016/j.steroids.2021.108912. Epub 2021 Sep 1. Steroids. 2021. PMID: 34480919

7

Novel A-Ring Chalcone Derivatives of Oleanolic and Ursolic Amides with Anti-Proliferative Effect Mediated through ROS-Triggered Apoptosis.

Khusnutdinova E, Petrova A, Zileeva Z, Kuzmina U, Zainullina L, Vakhitova Y, Babkov D, Kazakova O. Khusnutdinova E, et al. Among authors: petrova a. Int J Mol Sci. 2021 Sep 10;22(18):9796. doi: 10.3390/ijms22189796. Int J Mol Sci. 2021. PMID: 34575964 Free PMC article.

8

3-Pyridinylidene Derivatives of Chemically Modified Lupane and Ursane Triterpenes as Promising Anticancer Agents by Targeting Apoptosis.

Kazakova O, Șoica C, Babaev M, Petrova A, Khusnutdinova E, Poptsov A, Macașoi I, Drăghici G, Avram Ș, Vlaia L, Mioc A, Mioc M, Dehelean C, Voicu A. Kazakova O, et al. Among authors: petrova a. Int J Mol Sci. 2021 Oct 2;22(19):10695. doi: 10.3390/ijms221910695. Int J Mol Sci. 2021. PMID: 34639035 Free PMC article.

9

New Investigations with Lupane Type A-Ring Azepane Triterpenoids for Antimycobacterial Drug Candidate Design.

Kazakova O, Racoviceanu R, Petrova A, Mioc M, Militaru A, Udrescu L, Udrescu M, Voicu A, Cummings J, Robertson G, Ordway DJ, Slayden RA, Șoica C. Kazakova O, et al. Among authors: petrova a. Int J Mol Sci. 2021 Nov 21;22(22):12542. doi: 10.3390/ijms222212542. Int J Mol Sci. 2021. PMID: 34830423 Free PMC article.

10

Azepanodipterocarpol is potential candidate for inhibits influenza H1N1 type among other lupane, oleanane, and dammarane A-ring amino-triterpenoids.

Smirnova I, Petrova A, Lobov A, Minnibaeva E, Phoung TTT, Van LT, Khine MM, Esaulkova I, Slita A, Zarubaev V, Kazakova O. Smirnova I, et al. Among authors: petrova a. J Antibiot (Tokyo). 2022 May;75(5):258-267. doi: 10.1038/s41429-022-00514-w. Epub 2022 Mar 4. J Antibiot (Tokyo). 2022. PMID: 35246615 Free PMC article.

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