Alves MA - Search Results

1

New Leishmania donovani nucleoside hydrolase inhibitors from Brazilian flora.

Nirma C, Rangel GT, Alves MA, Casanova LM, Moreira MM, Rodrigues LM, Hamerski L, Tinoco LW. Nirma C, et al. Among authors: alves ma. RSC Adv. 2019 Jun 13;9(32):18663-18669. doi: 10.1039/c9ra02382h. eCollection 2019 Jun 10. RSC Adv. 2019. PMID: 35515226 Free PMC article.

2

Carbamoyl-N-aryl-imine-urea: a new framework to obtain a putative leishmanicidal drug-candidate.

Alves MA, de Queiroz AC, Leite AB, Martins FT, Doriguetto AC, Barreiro EJ, Alexandre-Moreira MS, Lima LM. Alves MA, et al. RSC Adv. 2020 Mar 26;10(21):12384-12394. doi: 10.1039/d0ra00287a. eCollection 2020 Mar 24. RSC Adv. 2020. PMID: 35497630 Free PMC article.

3

Discovery of naphthyl-N-acylhydrazone p38α MAPK inhibitors with in vivo anti-inflammatory and anti-TNF-α activity.

Freitas RHCN, Cordeiro NM, Carvalho PR, Alves MA, Guedes IA, Valerio TS, Dardenne LE, Lima LM, Barreiro EJ, Fernandes PD, Fraga CAM. Freitas RHCN, et al. Among authors: alves ma. Chem Biol Drug Des. 2018 Feb;91(2):391-397. doi: 10.1111/cbdd.13085. Epub 2017 Sep 10. Chem Biol Drug Des. 2018. PMID: 28815968

4

Monocyclic Nitro-heteroaryl Nitrones with Dual Mechanism of Activation: Synthesis and Antileishmanial Activity.

Pacheco JDS, Costa DS, Cunha-Júnior EF, Andrade-Neto VV, Fairlamb AH, Wyllie S, Goulart MOF, Santos DC, Silva TL, Alves MA, Costa PRR, Dias AG, Torres-Santos EC. Pacheco JDS, et al. Among authors: alves ma. ACS Med Chem Lett. 2021 Aug 16;12(9):1405-1412. doi: 10.1021/acsmedchemlett.1c00193. eCollection 2021 Sep 9. ACS Med Chem Lett. 2021. PMID: 34531949 Free PMC article.

5

Design, Synthesis, and Pharmacological Evaluation of First-in-Class Multitarget N-Acylhydrazone Derivatives as Selective HDAC6/8 and PI3Kα Inhibitors.

Rodrigues DA, Guerra FS, Sagrillo FS, de Sena M Pinheiro P, Alves MA, Thota S, Chaves LS, Sant'Anna CMR, Fernandes PD, Fraga CAM. Rodrigues DA, et al. Among authors: alves ma. ChemMedChem. 2020 Mar 18;15(6):539-551. doi: 10.1002/cmdc.201900716. Epub 2020 Feb 17. ChemMedChem. 2020. PMID: 32022441

6

Semicarbazone derivatives as promising therapeutic alternatives in leishmaniasis.

Cavalcanti de Queiroz A, Alves MA, Barreiro EJ, Lima LM, Alexandre-Moreira MS. Cavalcanti de Queiroz A, et al. Among authors: alves ma. Exp Parasitol. 2019 Jun;201:57-66. doi: 10.1016/j.exppara.2019.04.003. Epub 2019 Apr 17. Exp Parasitol. 2019. PMID: 31004571

7

Synthesis, biological evaluation, and structure-activity relationship of clonazepam, meclonazepam, and 1,4-benzodiazepine compounds with schistosomicidal activity.

Menezes CM, Rivera G, Alves MA, do Amaral DN, Thibaut JP, Noël F, Barreiro EJ, Lima LM. Menezes CM, et al. Among authors: alves ma. Chem Biol Drug Des. 2012 Jun;79(6):943-9. doi: 10.1111/j.1747-0285.2012.01354.x. Epub 2012 Mar 19. Chem Biol Drug Des. 2012. PMID: 22321778

8

3-Aminothiophene-2-acylhydrazones: non-toxic, analgesic and anti-inflammatory lead-candidates.

da Silva YK, Reyes CT, Rivera G, Alves MA, Barreiro EJ, Moreira MS, Lima LM. da Silva YK, et al. Among authors: alves ma. Molecules. 2014 Jun 20;19(6):8456-71. doi: 10.3390/molecules19068456. Molecules. 2014. PMID: 24955640 Free PMC article.

9

Design, synthesis and in vitro trypanocidal and leishmanicidal activities of novel semicarbazone derivatives.

Alves MA, de Queiroz AC, Alexandre-Moreira MS, Varela J, Cerecetto H, González M, Doriguetto AC, Landre IM, Barreiro EJ, Lima LM. Alves MA, et al. Eur J Med Chem. 2015 Jul 15;100:24-33. doi: 10.1016/j.ejmech.2015.05.046. Epub 2015 Jun 2. Eur J Med Chem. 2015. PMID: 26069927

10

Simple HPLC-UV for the quantification of a new leishmanicidal candidate (E)-1-4(trifluoromethyl) benzylidene)-5-(2-4-dichlorozoyl) carbonylhydrazine (LASSBio-1736) in rat plasma for pharmacokinetics assessment.

Moraes BKS, Bajerski L, Parisotto A, Silva CEDR, Alves MA, Barreiro EJ, Freddo RJ, Dalla Costa T, Lima LM, Haas SE. Moraes BKS, et al. Among authors: alves ma. Biomed Chromatogr. 2016 Jul;30(7):1029-1035. doi: 10.1002/bmc.3646. Epub 2016 Jan 3. Biomed Chromatogr. 2016. PMID: 26542632

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