Scotti MT - Search Results

1

Antileishmanial activity of new thiophene-indole hybrids: Design, synthesis, biological and cytotoxic evaluation, and chemometric studies.

Félix MB, de Souza ER, de Lima MDCA, Frade DKG, Serafim VL, Rodrigues KADF, Néris PLDN, Ribeiro FF, Scotti L, Scotti MT, de Aquino TM, Mendonça Junior FJB, de Oliveira MR. Félix MB, et al. Among authors: scotti l, scotti mt. Bioorg Med Chem. 2016 Sep 15;24(18):3972-3977. doi: 10.1016/j.bmc.2016.04.057. Epub 2016 Apr 26. Bioorg Med Chem. 2016. PMID: 27515718 Free article.

2

Quantitative structure-activity relationship of sesquiterpene lactones with cytotoxic activity.

Scotti MT, Fernandes MB, Ferreira MJ, Emerenciano VP. Scotti MT, et al. Bioorg Med Chem. 2007 Apr 15;15(8):2927-34. doi: 10.1016/j.bmc.2007.02.005. Epub 2007 Feb 11. Bioorg Med Chem. 2007. PMID: 17336532

3

Anti-leishmanial and anti-trypanosomal activities of 1,4-dihydropyridines: In vitro evaluation and structure-activity relationship study.

Reimão JQ, Scotti MT, Tempone AG. Reimão JQ, et al. Among authors: scotti mt. Bioorg Med Chem. 2010 Nov 15;18(22):8044-53. doi: 10.1016/j.bmc.2010.09.015. Epub 2010 Sep 15. Bioorg Med Chem. 2010. PMID: 20934347

4

Comparative computational studies of 3,4-dihydro-2,6-diaryl-4-oxo-pyrimidine-5-carbonitrile derivatives as potential antinociceptive agents.

dos Anjos JV, Srivastava RM, Costa-Silva JH, Scotti L, Scotti MT, Wanderley AG, Leite ES, de Melo SJ, Mendonça Junior FJ. dos Anjos JV, et al. Among authors: scotti l, scotti mt. Molecules. 2012 Jan 16;17(1):809-19. doi: 10.3390/molecules17010809. Molecules. 2012. PMID: 22249410 Free PMC article.

5

Self-organizing maps of molecular descriptors for sesquiterpene lactones and their application to the chemotaxonomy of the Asteraceae family.

Scotti MT, Emerenciano V, Ferreira MJ, Scotti L, Stefani R, da Silva MS, Mendonça Junior FJ. Scotti MT, et al. Among authors: scotti l. Molecules. 2012 Apr 20;17(4):4684-702. doi: 10.3390/molecules17044684. Molecules. 2012. PMID: 22522398 Free PMC article.

6

Preliminary antifungal and cytotoxic evaluation of synthetic cycloalkyl[b]thiophene derivatives with PLS-DA analysis.

Souza BC, De Oliveira TB, Aquino TM, de Lima MC, Pitta IR, Galdino SL, Lima EO, Gonçalves-Silva T, Militão GC, Scotti L, Scotti MT, Mendonça FJ Jr. Souza BC, et al. Among authors: scotti l, scotti mt. Acta Pharm. 2012 Jun;62(2):221-36. doi: 10.2478/v10007-012-0017-y. Acta Pharm. 2012. PMID: 22750820 Free article.

7

Synthesis, structure-activity relationships (SAR) and in silico studies of coumarin derivatives with antifungal activity.

de Araújo RS, Guerra FQ, de O Lima E, de Simone CA, Tavares JF, Scotti L, Scotti MT, de Aquino TM, de Moura RO, Mendonça FJ, Barbosa-Filho JM. de Araújo RS, et al. Among authors: scotti l, scotti mt. Int J Mol Sci. 2013 Jan 10;14(1):1293-309. doi: 10.3390/ijms14011293. Int J Mol Sci. 2013. PMID: 23306152 Free PMC article.

8

Quantitative structure-sorption relationships of pesticides used in the sugarcane industry in the northern coastal area of Paraíba State, Brazil.

da S Soares GC, de M e Silva L, de A Farias CH, Scotti L, Scotti MT. da S Soares GC, et al. Among authors: scotti l, scotti mt. Altern Lab Anim. 2014 Mar;42(1):81-90. doi: 10.1177/026119291404200111. Altern Lab Anim. 2014. PMID: 24773491 Free article.

9

Synthesis and preliminary ex vivo evaluation of the spasmolytic activity of 1,3-thiazolium- and 1,3,4-thiadiazolium-5-methylthio- and 5-thioacetate derivatives.

Luis JA, Aquino TM, Lira BF, Filho PF, Scotti MT, Scotti L, Moura RO, Junior FJ. Luis JA, et al. Among authors: scotti l, scotti mt. Acta Pharm. 2014 Jun;64(2):233-45. doi: 10.2478/acph-2014-0016. Acta Pharm. 2014. PMID: 24914723 Free article.

10

Benzo- and thienobenzo- diazepines: multi-target drugs for CNS disorders.

Mendonça Júnior FJ, Scotti L, Ishiki H, Botelho SP, Da Silva MS, Scotti MT. Mendonça Júnior FJ, et al. Among authors: scotti l, scotti mt. Mini Rev Med Chem. 2015;15(8):630-47. doi: 10.2174/1389557515666150219125030. Mini Rev Med Chem. 2015. PMID: 25694077 Review.

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