Detalhe da pesquisa
1.
Novel Organic Salts Based on Mefloquine: Synthesis, Solubility, Permeability, and In Vitro Activity against Mycobacterium tuberculosis.
Molecules
; 27(16)2022 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36014405
2.
Mefloquine synergism with anti-tuberculosis drugs and correlation to membrane effects: Biologic, spectroscopic and molecular dynamics simulations studies.
Bioorg Chem
; 110: 104786, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33740676
3.
Synthesis and evaluation of copper(II) complexes with isoniazid-derived hydrazones as anticancer and antitubercular agents.
Biometals
; 29(6): 953-963, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27591998
4.
Anti-tuberculosis evaluation and conformational study of N-acylhydrazones containing the thiophene nucleus.
Arch Pharm (Weinheim)
; 347(6): 432-48, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24616002
5.
Mefloquine-oxazolidine derivatives, derived from mefloquine and arenecarbaldehydes: In vitro activity including against the multidrug-resistant tuberculosis strain T113.
Bioorg Med Chem
; 20(1): 243-8, 2012 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22142615
6.
Novel 2-Nitroimidazole and Imidazooxazole Derivatives and their Activity against Trypanosoma cruzi and Mycobacterium tuberculosis.
Med Chem
; 18(6): 701-709, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34784878
7.
Synthesis, antitubercular activity, and SAR study of N-substituted-phenylamino-5-methyl-1H-1,2,3-triazole-4-carbohydrazides.
Bioorg Med Chem
; 19(18): 5605-11, 2011 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21840219
8.
Synthesis, Antitrypanosomal and Antimycobacterial Activities of Coumarin N-acylhydrazonic Derivatives.
Med Chem
; 17(6): 630-637, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-31965946
9.
Synthesis of alpha- and beta-pyran naphthoquinones as a new class of antitubercular agents.
Arch Pharm (Weinheim)
; 343(2): 81-90, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20077521
10.
Synthesis and antitubercular activity of heteroaromatic isonicotinoyl and 7-chloro-4-quinolinyl hydrazone derivatives.
ScientificWorldJournal
; 10: 1347-55, 2010 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20623095
11.
Benzoylthioureas: Design, Synthesis and Antimycobacterial Evaluation.
Med Chem
; 16(1): 93-103, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-30526466
12.
Synthesis and antitubercular activity of 7-chloro-4-quinolinylhydrazones derivatives.
Bioorg Med Chem Lett
; 19(22): 6272-4, 2009 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19819134
13.
Synthesis and in vitro antitubercular activity of a series of quinoline derivatives.
Bioorg Med Chem
; 17(4): 1474-80, 2009 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19188070
14.
Synthesis and Antibacterial Activity of Mefloquine-Based Analogs Against Sensitive and Resistant Mycobacterium tuberculosis Strains.
Curr Top Med Chem
; 19(9): 683-689, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30836914
15.
Cutaneous tuberculosis in Rio de Janeiro, Brazil: description of a series of 75 cases.
Int J Dermatol
; 58(12): 1451-1459, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31553059
16.
Synthesis and antimycobacterial evaluation of new trans-cinnamic acid hydrazide derivatives.
Bioorg Med Chem Lett
; 18(2): 538-41, 2008 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18068364
17.
Preparation and antitubercular activities of alkylated amino alcohols and their glycosylated derivatives.
Bioorg Med Chem
; 15(24): 7789-94, 2007 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17851083
18.
Anti-Mycobacterial Evaluation of 7-Chloro-4-Aminoquinolines and Hologram Quantitative Structure-Activity Relationship (HQSAR) Modeling of Amino-Imino Tautomers.
Pharmaceuticals (Basel)
; 10(2)2017 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28598408
19.
Synthesis, Antitubercular and Anticancer Activities of p-nitrophenylethylenediamine-derived Schiff Bases.
Med Chem
; 2016 Nov 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27823561
20.
Syntheses and antimycobacterial activities of [(2S,3R)-2-(amino)-4-(arenesulfonamido)-3-hydroxy-1-phenylbutane derivatives.
Med Chem
; 10(2): 189-200, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23627296