FAQ

Anilide analgesics and antipyretics

Known as: Anilides 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1959-2018
02419592018

Related topics

Related topics

1 relation
Anilides

Related mentions per year

Related mentions per year

1938-2018
19401960198020002020
Anilide analgesics and antipyretics
Anilides

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Anilides and quinolones with nitrogen-bearing substituents from benzothiophene and thienothiophene series: synthesis, photochemical synthesis, cytostatic evaluation, 3D-derived QSAR analysis and DNA…
A series of new anilides (2a-c, 4-7, 17a-c, 18) and quinolones (3a-b, 8a-b, 9a-b, 10-15, 19) with nitrogen-bearing substituents… (More)
  • figure 1
  • figure 3
  • figure 2
  • figure 4
  • table 1
Is this relevant?
2013
2013
Synthesis and antimycobacterial evaluation of N-substituted 5-chloropyrazine-2-carboxamides.
To develop new potential antimycobacterial drugs, a series of pyrazinamide derivatives was designed, synthesized and tested for… (More)
Is this relevant?
2012
2012
Effect of competition bias in safety signal generation: analysis of a research database of spontaneous reports in France.
BACKGROUND Automated disproportionality analysis of spontaneous reporting is increasingly used routinely. It can theoretically be… (More)
  • table I
  • table II
  • table III
  • table IV
Is this relevant?
2011
2011
Mild C-H halogenation of anilides and the isolation of an unusual palladium(I)-palladium(II) species.
by Shi and co-workers who demonstrated that anilides could be ortho chlorinated in good to excellent yields using Pd(OAc)2 as the… (More)
  • table 1
  • table 2
  • figure 1
Is this relevant?
2008
2008
Direct ortho-acetoxylation of anilides via palladium-catalyzed sp(2) C-H bond oxidative activation.
Various anilides have been directly ortho-acetoxylated through a Pd(OAc)2-catalyzed C-H bond activation process. The amide group… (More)
Is this relevant?
2005
2005
Discovery of potent anilide inhibitors against the severe acute respiratory syndrome 3CL protease.
A diversified library of peptide anilides was prepared, and their inhibition activities against the SARS-CoV 3CL protease were… (More)
  • figure 1
  • table 1
  • figure 2
Is this relevant?
2003
2003
Development of potential antitumor agents. Synthesis and biological evaluation of a new set of sulfonamide derivatives as histone deacetylase inhibitors.
A series of sulfonamide hydroxamic acids and anilides have been synthesized and studied as histone deacetylase (HDAC) inhibitors… (More)
Is this relevant?
2002
2002
Sulfonamide anilides, a novel class of histone deacetylase inhibitors, are antiproliferative against human tumors.
Inhibition of histone deacetylases (HDACs) is emerging as a new strategy in human cancer therapy. We have designed and… (More)
  • table 1
  • figure 1
  • table 2
  • figure 3
  • figure 2
Is this relevant?
2001
2001
Storage time and deodorization temperature influence the formation of aniline-derived compounds in denatured rapeseed oils.
In 1981 an epidemic, named Toxic Oil Syndrome, occurred in Spain as a result of ingestion of rapeseed oil denatured with 2… (More)
Is this relevant?
1995
1995
Structure-activity relationships for inhibition of type 1 and 2 human 5 alpha-reductase and human adrenal 3 beta-hydroxy-delta 5-steroid dehydrogenase/3-keto-delta 5-steroid isomerase by 6-azaandrost…
A variety of C17 amide-substituted 6-azaandrost-4-en-3-ones were prepared and tested versus human type 1 and 2 steroid 5 alpha… (More)
Is this relevant?