Montanari CA - Search Results

1

Can Cysteine Protease Cross-Class Inhibitors Achieve Selectivity?

Cianni L, Feldmann CW, Gilberg E, Gütschow M, Juliano L, Leitão A, Bajorath J, Montanari CA. Cianni L, et al. Among authors: montanari ca. J Med Chem. 2019 Dec 12;62(23):10497-10525. doi: 10.1021/acs.jmedchem.9b00683. Epub 2019 Aug 15. J Med Chem. 2019. PMID: 31361135 Review.

2

Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase.

Leitão A, Andricopulo AD, Oliva G, Pupo MT, de Marchi AA, Vieira PC, da Silva MF, Ferreira VF, de Souza MC, Sá MM, Moraes VR, Montanari CA. Leitão A, et al. Among authors: montanari ca. Bioorg Med Chem Lett. 2004 May 3;14(9):2199-204. doi: 10.1016/j.bmcl.2004.02.025. Bioorg Med Chem Lett. 2004. PMID: 15081008

3

Three-dimensional models of non-steroidal ligands: a comparative molecular field analysis.

Menezes IR, Leitão A, Montanari CA. Menezes IR, et al. Among authors: montanari ca. Steroids. 2006 Jun;71(6):417-28. doi: 10.1016/j.steroids.2006.01.001. Epub 2006 Feb 14. Steroids. 2006. PMID: 16481019

4

The role of molecular interaction fields on enantioselective and nonselective separation of chiral sulfoxides.

Montanari ML, Cass QB, Leitão A, Andricopulo AD, Montanari CA. Montanari ML, et al. Among authors: montanari ca. J Chromatogr A. 2006 Jul 14;1121(1):64-75. doi: 10.1016/j.chroma.2006.04.072. Epub 2006 May 22. J Chromatogr A. 2006. PMID: 16716332

5

The molecular retention mechanism in reversed-phase liquid chromatography of meso-ionic compounds by quantitative structure-retention relationships (QSRR).

Almeida TM, Leitão A, Montanari ML, Montanari CA. Almeida TM, et al. Among authors: montanari ca, montanari ml. Chem Biodivers. 2005 Dec;2(12):1691-700. doi: 10.1002/cbdv.200590139. Chem Biodivers. 2005. PMID: 17191966

6

In silico screening of HIV-1 non-nucleoside reverse transcriptase and protease inhibitors.

Leitão A, Andricopulo AD, Montanari CA. Leitão A, et al. Among authors: montanari ca. Eur J Med Chem. 2008 Jul;43(7):1412-22. doi: 10.1016/j.ejmech.2007.08.017. Epub 2007 Sep 19. Eur J Med Chem. 2008. PMID: 17954002

7

2D QSAR and similarity studies on cruzain inhibitors aimed at improving selectivity over cathepsin L.

Freitas RF, Oprea TI, Montanari CA. Freitas RF, et al. Among authors: montanari ca. Bioorg Med Chem. 2008 Jan 15;16(2):838-53. doi: 10.1016/j.bmc.2007.10.048. Epub 2007 Oct 22. Bioorg Med Chem. 2008. PMID: 17996450

8

Novel insights for dihydroorotate dehydrogenase class 1A inhibitors discovery.

Cheleski J, Rocha JR, Pinheiro MP, Wiggers HJ, da Silva AB, Nonato MC, Montanari CA. Cheleski J, et al. Among authors: montanari ca. Eur J Med Chem. 2010 Dec;45(12):5899-909. doi: 10.1016/j.ejmech.2010.09.055. Epub 2010 Oct 7. Eur J Med Chem. 2010. PMID: 20965617

9

Comparative molecular field analysis of a series of inhibitors of HIV-1 protease.

Ferreira LG, Leitão A, Montanari CA, Andricopulo AD. Ferreira LG, et al. Among authors: montanari ca. Med Chem. 2011 Mar;7(2):71-9. doi: 10.2174/157340611794859370. Med Chem. 2011. PMID: 21222610

10

Molecular design, synthesis and biological evaluation of 1,4-dihydro-4-oxoquinoline ribonucleosides as TcGAPDH inhibitors with trypanocidal activity.

Soares FA, Sesti-Costa R, da Silva JS, de Souza MC, Ferreira VF, Santos Fda C, Monteiro PA, Leitão A, Montanari CA. Soares FA, et al. Among authors: montanari ca. Bioorg Med Chem Lett. 2013 Aug 15;23(16):4597-601. doi: 10.1016/j.bmcl.2013.06.029. Epub 2013 Jun 24. Bioorg Med Chem Lett. 2013. PMID: 23850203

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