Vasilakaki S - Search Results

1

A facile consensus ranking approach enhances virtual screening robustness and identifies a cell-active DYRK1α inhibitor.

Mavrogeni ME, Pronios F, Zareifi D, Vasilakaki S, Lozach O, Alexopoulos L, Meijer L, Myrianthopoulos V, Mikros E. Mavrogeni ME, et al. Among authors: vasilakaki s. Future Med Chem. 2018 Oct;10(20):2411-2430. doi: 10.4155/fmc-2018-0198. Epub 2018 Oct 16. Future Med Chem. 2018. PMID: 30325204 Free PMC article.

2

Novel Aryl-Substituted Pyrimidones as Inhibitors of 3-Mercaptopyruvate Sulfurtransferase with Antiproliferative Efficacy in Colon Cancer.

Bantzi M, Augsburger F, Loup J, Berset Y, Vasilakaki S, Myrianthopoulos V, Mikros E, Szabo C, Bochet CG. Bantzi M, et al. Among authors: vasilakaki s. J Med Chem. 2021 May 13;64(9):6221-6240. doi: 10.1021/acs.jmedchem.1c00260. Epub 2021 Apr 15. J Med Chem. 2021. PMID: 33856792

3

Development of a potent 2-oxoamide inhibitor of secreted phospholipase A2 guided by molecular docking calculations and molecular dynamics simulations.

Vasilakaki S, Barbayianni E, Leonis G, Papadopoulos MG, Mavromoustakos T, Gelb MH, Kokotos G. Vasilakaki S, et al. Bioorg Med Chem. 2016 Apr 15;24(8):1683-95. doi: 10.1016/j.bmc.2016.02.040. Epub 2016 Mar 2. Bioorg Med Chem. 2016. PMID: 26970660 Free PMC article.

4

Inhibitors of secreted phospholipase A2 suppress the release of PGE2 in renal mesangial cells.

Vasilakaki S, Barbayianni E, Magrioti V, Pastukhov O, Constantinou-Kokotou V, Huwiler A, Kokotos G. Vasilakaki S, et al. Bioorg Med Chem. 2016 Jul 1;24(13):3029-3034. doi: 10.1016/j.bmc.2016.05.017. Epub 2016 May 13. Bioorg Med Chem. 2016. PMID: 27234891

5

Using physics-based pose predictions and free energy perturbation calculations to predict binding poses and relative binding affinities for FXR ligands in the D3R Grand Challenge 2.

Athanasiou C, Vasilakaki S, Dellis D, Cournia Z. Athanasiou C, et al. Among authors: vasilakaki s. J Comput Aided Mol Des. 2018 Jan;32(1):21-44. doi: 10.1007/s10822-017-0075-9. Epub 2017 Nov 8. J Comput Aided Mol Des. 2018. PMID: 29119352

6

α-Ketoheterocycles Able to Inhibit the Generation of Prostaglandin E₂ (PGE₂) in Rat Mesangial Cells.

Psarra A, Theodoropoulou MA, Erhardt M, Mertiri M, Mantzourani C, Vasilakaki S, Magrioti V, Huwiler A, Kokotos G. Psarra A, et al. Among authors: vasilakaki s. Biomolecules. 2021 Feb 13;11(2):275. doi: 10.3390/biom11020275. Biomolecules. 2021. PMID: 33668480 Free PMC article.

7

The design and discovery of phospholipase A₂ inhibitors for the treatment of inflammatory diseases.

Batsika CS, Gerogiannopoulou AD, Mantzourani C, Vasilakaki S, Kokotos G. Batsika CS, et al. Among authors: vasilakaki s. Expert Opin Drug Discov. 2021 Nov;16(11):1287-1305. doi: 10.1080/17460441.2021.1942835. Epub 2021 Jul 15. Expert Opin Drug Discov. 2021. PMID: 34143707 Review.

8

Small Peptides Able to Suppress Prostaglandin E₂ Generation in Renal Mesangial Cells.

Vasilakaki S, Pastukhov O, Mavromoustakos T, Huwiler A, Kokotos G. Vasilakaki S, et al. Molecules. 2018 Jan 13;23(1):158. doi: 10.3390/molecules23010158. Molecules. 2018. PMID: 29342835 Free PMC article.

9

Small-molecule inhibitors as potential therapeutics and as tools to understand the role of phospholipases A₂.

Nikolaou A, Kokotou MG, Vasilakaki S, Kokotos G. Nikolaou A, et al. Among authors: vasilakaki s. Biochim Biophys Acta Mol Cell Biol Lipids. 2019 Jun;1864(6):941-956. doi: 10.1016/j.bbalip.2018.08.009. Epub 2018 Aug 23. Biochim Biophys Acta Mol Cell Biol Lipids. 2019. PMID: 30905350 Free PMC article. Review.

10

Corrigendum to "Small-molecule inhibitors as potential therapeutics and as tools to understand the role of phospholipases A2" [Biochim. Biophys. Acta Mol. Cell Biol. Lipids 1864/6 2019 941-956].

Nikolaou A, Kokotou MG, Vasilakaki S, Kokotos G. Nikolaou A, et al. Among authors: vasilakaki s. Biochim Biophys Acta Mol Cell Biol Lipids. 2019 Nov;1864(11):1681. doi: 10.1016/j.bbalip.2019.06.009. Epub 2019 Jun 17. Biochim Biophys Acta Mol Cell Biol Lipids. 2019. PMID: 31221540 Free PMC article. No abstract available.

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