Baltas M - Search Results

1

Distinct CCK-2 receptor conformations associated with β-arrestin-2 recruitment or phospholipase-C activation revealed by a biased antagonist.

Magnan R, Escrieut C, Gigoux V, De K, Clerc P, Niu F, Azema J, Masri B, Cordomi A, Baltas M, Tikhonova IG, Fourmy D. Magnan R, et al. Among authors: baltas m. J Am Chem Soc. 2013 Feb 20;135(7):2560-73. doi: 10.1021/ja308784w. Epub 2013 Feb 6. J Am Chem Soc. 2013. PMID: 23323542

2

Recent advances in the development of cinnamic-like derivatives as antituberculosis agents.

De P, De K, Veau D, Bedos-Belval F, Chassaing S, Baltas M. De P, et al. Among authors: baltas m. Expert Opin Ther Pat. 2012 Feb;22(2):155-68. doi: 10.1517/13543776.2012.661717. Epub 2012 Feb 14. Expert Opin Ther Pat. 2012. PMID: 22329571 Review.

3

Antimalarial bicyclic peroxides belonging to the G-factor family: mechanistic aspects of their formation and iron (II) induced reduction.

Ruiz J, Azema J, Payrastre C, Baltas M, Tuccio B, Vial H, Andre-Barres C. Ruiz J, et al. Among authors: baltas m. Curr Top Med Chem. 2014;14(14):1668-83. doi: 10.2174/1568026614666140808154326. Curr Top Med Chem. 2014. PMID: 25116578

4

Rational inhibitor design, synthesis and NMR spectroscopic study by transferred nuclear overhauser spectroscopy of novel inhibitors of cinnamyl alcohol dehydrogenase, a critical enzyme in lignification.

Kennedy K, Baltas M, Douglas KT, Duran H, Embrey KJ, Giraudon JG, McKie JH, Grima-Pettenati J, Gorrichon L. Kennedy K, et al. Among authors: baltas m. J Enzyme Inhib. 1999;14(3):217-37. doi: 10.3109/14756369909030318. J Enzyme Inhib. 1999. PMID: 10445045

5

Concise asymmetric syntheses of (-)-lentiginosine and of its pyrrolizidinic analogue.

Ayad T, Génisson Y, Baltas M, Gorrichon L. Ayad T, et al. Among authors: baltas m. Chem Commun (Camb). 2003 Mar 7;(5):582-3. doi: 10.1039/b212217k. Chem Commun (Camb). 2003. PMID: 12669835

6

Synthesis and biological evaluation of conformationally constrained analogues of the antitubercular agent ethambutol.

Faugeroux V, Génisson Y, Salma Y, Constant P, Baltas M. Faugeroux V, et al. Among authors: baltas m. Bioorg Med Chem. 2007 Sep 1;15(17):5866-76. doi: 10.1016/j.bmc.2007.05.064. Epub 2007 Jun 2. Bioorg Med Chem. 2007. PMID: 17566744

7

Chemical synthesis and biological evaluation of triazole derivatives as inhibitors of InhA and antituberculosis agents.

Menendez C, Chollet A, Rodriguez F, Inard C, Pasca MR, Lherbet C, Baltas M. Menendez C, et al. Among authors: baltas m. Eur J Med Chem. 2012 Jun;52:275-83. doi: 10.1016/j.ejmech.2012.03.029. Epub 2012 Mar 23. Eur J Med Chem. 2012. PMID: 22483635

8

Design, chemical synthesis of 3-(9H-fluoren-9-yl)pyrrolidine-2,5-dione derivatives and biological activity against enoyl-ACP reductase (InhA) and Mycobacterium tuberculosis.

Matviiuk T, Rodriguez F, Saffon N, Mallet-Ladeira S, Gorichko M, de Jesus Lopes Ribeiro AL, Pasca MR, Lherbet C, Voitenko Z, Baltas M. Matviiuk T, et al. Among authors: baltas m. Eur J Med Chem. 2013;70:37-48. doi: 10.1016/j.ejmech.2013.09.041. Epub 2013 Oct 2. Eur J Med Chem. 2013. PMID: 24140915

9

Design, synthesis and evaluation of new GEQ derivatives as inhibitors of InhA enzyme and Mycobacterium tuberculosis growth.

Chollet A, Mori G, Menendez C, Rodriguez F, Fabing I, Pasca MR, Madacki J, Korduláková J, Constant P, Quémard A, Bernardes-Génisson V, Lherbet C, Baltas M. Chollet A, et al. Among authors: baltas m. Eur J Med Chem. 2015 Aug 28;101:218-35. doi: 10.1016/j.ejmech.2015.06.035. Epub 2015 Jun 20. Eur J Med Chem. 2015. PMID: 26142487

10

In Silico Repositioning of Cannabigerol as a Novel Inhibitor of the Enoyl Acyl Carrier Protein (ACP) Reductase (InhA).

Pinzi L, Lherbet C, Baltas M, Pellati F, Rastelli G. Pinzi L, et al. Among authors: baltas m. Molecules. 2019 Jul 15;24(14):2567. doi: 10.3390/molecules24142567. Molecules. 2019. PMID: 31311157 Free PMC article.

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