Similar articles for PMID: 25462252

Year	Number of Results
1976	1
1986	2
1990	1
1992	1
1993	1
1996	1
1997	1
2000	2
2001	2
2002	1
2003	6
2004	1
2005	9
2006	7
2007	5
2008	8
2009	11
2010	15
2011	8
2012	9
2013	14
2014	22
2015	20
2016	19
2017	17
2018	21
2019	14
2020	16
2021	5
2022	5
2023	3
2024	0

1

Design, synthesis and anti-leishmanial activity of novel symmetrical bispyridinium cyclophanes.

Gómez-Pérez V, Manzano JI, García-Hernández R, Castanys S, Gamarro F, Campos JM. Gómez-Pérez V, et al. Eur J Med Chem. 2015 Jan 7;89:362-9. doi: 10.1016/j.ejmech.2014.10.040. Epub 2014 Oct 16. Eur J Med Chem. 2015. PMID: 25462252

2

4-amino bis-pyridinium derivatives as novel antileishmanial agents.

Gómez-Pérez V, Manzano JI, García-Hernández R, Castanys S, Campos Rosa JM, Gamarro F. Gómez-Pérez V, et al. Antimicrob Agents Chemother. 2014 Jul;58(7):4103-12. doi: 10.1128/AAC.02481-13. Epub 2014 May 5. Antimicrob Agents Chemother. 2014. PMID: 24798287 Free PMC article.

3

GRIND2-based 3D-QSAR and prediction of activity spectra for symmetrical bis-pyridinium salts with promastigote antileishmanial activity.

Diniz EMLP, Tomich de Paula da Silva CH, Gómez-Perez V, Federico LB, Campos Rosa JM. Diniz EMLP, et al. J Biomol Struct Dyn. 2017 Aug;35(11):2430-2440. doi: 10.1080/07391102.2016.1221364. Epub 2016 Sep 6. J Biomol Struct Dyn. 2017. PMID: 27495391

4

Synthesis and antileishmanial activity of novel pyridinium-hydrazone derivatives.

Alptuzun V, Cakiroglu G, Limoncu ME, Erac B, Hosgor-Limoncu M, Erciyas E. Alptuzun V, et al. J Enzyme Inhib Med Chem. 2013 Oct;28(5):960-7. doi: 10.3109/14756366.2012.697058. Epub 2012 Jul 18. J Enzyme Inhib Med Chem. 2013. PMID: 22803671

5

Design, synthesis and evaluation of amino-substituted 1H-phenalen-1-ones as anti-leishmanial agents.

Freijo MB, López-Arencibia A, Piñero JE, McNaughton-Smith G, Abad-Grillo T. Freijo MB, et al. Eur J Med Chem. 2018 Jan 1;143:1312-1324. doi: 10.1016/j.ejmech.2017.10.032. Epub 2017 Oct 14. Eur J Med Chem. 2018. PMID: 29126735

6

Biological evaluation and structure activity relationship of 9-methyl-1-phenyl-9H-pyrido[3,4-b]indole derivatives as anti-leishmanial agents.

Ashok P, Chander S, Smith TK, Prakash Singh R, Jha PN, Sankaranarayanan M. Ashok P, et al. Bioorg Chem. 2019 Mar;84:98-105. doi: 10.1016/j.bioorg.2018.11.037. Epub 2018 Nov 22. Bioorg Chem. 2019. PMID: 30500524 Free PMC article.

7

Synthesis and biological evaluation of 2-arylbenzimidazoles targeting Leishmania donovani.

Keurulainen L, Siiskonen A, Nasereddin A, Kopelyanskiy D, Sacerdoti-Sierra N, Leino TO, Tammela P, Yli-Kauhaluoma J, Jaffe CL, Kiuru P. Keurulainen L, et al. Bioorg Med Chem Lett. 2015 May 1;25(9):1933-7. doi: 10.1016/j.bmcl.2015.03.027. Epub 2015 Mar 18. Bioorg Med Chem Lett. 2015. PMID: 25827525

8

Design, synthesis and biological evaluation of aryl pyrimidine derivatives as potential leishmanicidal agents.

Suryawanshi SN, Kumar S, Shivahare R, Pandey S, Tiwari A, Gupta S. Suryawanshi SN, et al. Bioorg Med Chem Lett. 2013 Sep 15;23(18):5235-8. doi: 10.1016/j.bmcl.2013.06.060. Epub 2013 Jun 29. Bioorg Med Chem Lett. 2013. PMID: 23910597

9

Synthesis and evaluation of new furanyl and thiophenyl azoles as antileishmanial agents.

Marrapu VK, Mittal M, Shivahare R, Gupta S, Bhandari K. Marrapu VK, et al. Eur J Med Chem. 2011 May;46(5):1694-700. doi: 10.1016/j.ejmech.2011.02.021. Epub 2011 Feb 22. Eur J Med Chem. 2011. PMID: 21385661

10

Synthesis and antikinetoplastid activities of 3-substituted quinolinones derivatives.

Audisio D, Messaoudi S, Cojean S, Peyrat JF, Brion JD, Bories C, Huteau F, Loiseau PM, Alami M. Audisio D, et al. Eur J Med Chem. 2012 Jun;52:44-50. doi: 10.1016/j.ejmech.2012.03.003. Epub 2012 Mar 16. Eur J Med Chem. 2012. PMID: 22472166

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