Synthesis and evaluation of anti-Toxoplasma gondii and antimicrobial activities of thiosemicarbazides, 4-thiazolidinones and 1,3,4-thiadiazoles.
about
Discovery of potential anti-infectives against Staphylococcus aureus using a Caenorhabditis elegans infection model.Synthesis, DNA Binding, and Antiproliferative Activity of Novel Acridine-Thiosemicarbazone DerivativesSynthesis, Structure and Antioxidant Activity of (Tetra-O-acetyl-β-D-galactopyranosyl)thiosemicarbazones of Substituted BenzaldehydesSynthesis and biological evaluation of new 1,3-thiazolidine-4-one derivatives of nitro-l-arginine methyl esterA Systematic Review of In vitro and In vivo Activities of Anti-Toxoplasma Drugs and Compounds (2006-2016).Drugs in development for toxoplasmosis: advances, challenges, and current status.Thiadiazole-a promising structure in medicinal chemistry.1,4-Disubstituted thiosemicarbazide derivatives are potent inhibitors of Toxoplasma gondii proliferation.Thiadiazoles: the appropriate pharmacological scaffolds with leishmanicidal and antimalarial activities: a review.Synthesis and antimicrobial evaluation of some novel 1,2,4-triazole and 1,3,4-thiadiazole derivatives.2-(4-Oxo-3-phenyl-1,3-thia-zolidin-2-yl-idene)malononitrile.Synthesis and antioxidant activity evaluation of new compounds from hydrazinecarbothioamide and 1,2,4-triazole class containing diarylsulfone and 2,4-difluorophenyl moietiesOrganocatalysis in heterocyclic synthesis: DABCO as a mild and efficient catalytic system for the synthesis of a novel class of quinazoline, thiazolo [3,2-a]quinazoline and thiazolo[2,3-b] quinazoline derivatives.Structural design, synthesis and structure-activity relationships of thiazolidinones with enhanced anti-Trypanosoma cruzi activity.A Perspective on Thiazolidinone Scaffold Development as a New Therapeutic Strategy for ToxoplasmosisStereochemical Investigations of Diastereomeric N-[2-(Aryl)-5-methyl-4-oxo-1,3-thiazolidine-3-yl]-pyridine-3-carboxamides by Nuclear Magnetic Resonance Spectroscopy (1D and 2D)
P2860
Q35083772-0CD7C042-2BFD-43AF-B635-CAE88A8AA732Q35813958-20E0DA0E-DB20-4D35-9689-FD57E6AA1017Q36426038-E8CD2CF3-A7A3-4EF4-992F-6E6F7DDF33FEQ36549942-3EC23241-A10B-4444-97CD-57C413C69543Q37594988-E1737AAD-4094-46DE-BF05-92BBDC6EC4FCQ37613765-BC2430CB-49A5-4876-8EFC-EA13707532CBQ38064804-AA9D3CFF-BEEB-4169-AE77-2D2B7AC44713Q38976714-66376F78-5004-4652-80CE-186FD3D1BE63Q39505293-71C9480A-B856-4500-94D8-68679812115DQ40955645-34D97A80-0C66-452D-AAA7-D6E0E94168C1Q41596791-8FE88997-C593-4943-B094-500BE4BCA750Q41964581-0F530B62-E067-4139-B5AC-82CB2A1081F2Q42116015-69EFD8D2-91FE-4E46-B775-1DC97EA61D3FQ54644826-038A7969-F05A-4244-91DB-39AB7E3EE113Q58553452-1E379A13-D576-4CDA-AA41-EADB10D731FCQ59111155-38C34F12-3BF5-4333-8643-BAEC83396D73
P2860
Synthesis and evaluation of anti-Toxoplasma gondii and antimicrobial activities of thiosemicarbazides, 4-thiazolidinones and 1,3,4-thiadiazoles.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Synthesis and evaluation of an ...... inones and 1,3,4-thiadiazoles.
@en
Synthesis and evaluation of an ...... inones and 1,3,4-thiadiazoles.
@nl
type
label
Synthesis and evaluation of an ...... inones and 1,3,4-thiadiazoles.
@en
Synthesis and evaluation of an ...... inones and 1,3,4-thiadiazoles.
@nl
prefLabel
Synthesis and evaluation of an ...... inones and 1,3,4-thiadiazoles.
@en
Synthesis and evaluation of an ...... inones and 1,3,4-thiadiazoles.
@nl
P2093
P1476
Synthesis and evaluation of an ...... inones and 1,3,4-thiadiazoles.
@en
P2093
Alexandre J S Góes
André P Liesen
Anselmo Q Alves
Antonio J Alves
Antônio R de Faria
Cristiane S Carvalho
Edésio J T de Melo
Elias W Alves
Janete M de Araújo
José G de Lima
P304
P356
10.1016/J.EJMECH.2010.05.017
P577
2010-05-31T00:00:00Z