Anilides

Known as: Anilides [Chemical/Ingredient], anilide 
Any aromatic amide obtained by acylation of aniline.
National Institutes of Health

Related topics

Related topics

50 relations

Narrower (46)

1045U852-(2-propynyl)tosylanilide2-(hydroxy)-3-octyn carboxanilide2-(methylseleninyl)benzanilide
(More)
In Bloodagonistsantagonists & inhibitorschemical synthesis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Cinnamic anilides as new mitochondrial permeability transition pore inhibitors endowed with ischemia-reperfusion injury protective effect in vivo.
In this account, we report the development of a series of substituted cinnamic anilides that represents a novel class of… (More)
  • figure 1
  • figure 2
  • table 1
  • figure 3
  • table 2
Is this relevant?
2007
2007
Design and synthesis of anticonvulsants from a combined phthalimide-GABA-anilide and hydrazone pharmacophore.
Two series of pharmacophoric hybrids of phthalimide-GABA-anilides/hydrazones were designed and synthesized and evaluated for… (More)
Is this relevant?
Highly Cited
2004
Highly Cited
2004
Histone deacetylase inhibitors have a profound antigrowth activity in endometrial cancer cells.
PURPOSE HDAC inhibitors (HDACIs) have been shown to inhibit cancer cell proliferation, stimulate apoptosis, and induce cell cycle… (More)
  • figure 1
  • table 1
  • table 2
  • figure 2
  • figure 3
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?
2000
2000
Anilide derivatives of an 8-phenylxanthine carboxylic congener are highly potent and selective antagonists at human A(2B) adenosine receptors.
No highly selective antagonists of the A(2B) adenosine receptor (AR) have been reported; however such antagonists have… (More)
Is this relevant?
2000
2000
Anilides of (R)-trifluoro-2-hydroxy-2-methylpropionic acid as inhibitors of pyruvate dehydrogenase kinase.
The optimization of a series of anilide derivatives of (R)-3,3, 3-trifluoro-2-hydroxy-2-methylpropionic acid as inhibitors of… (More)
Is this relevant?
Highly Cited
1999
Highly Cited
1999
Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives.
Newly synthesized benzamide derivatives were evaluated for their inhibitory activity against histone deacetylase. The structure… (More)
  • table 1
Is this relevant?
Highly Cited
1998
Highly Cited
1998
In vivo characterization of the drug resistance profile of the major ABC transporters and other components of the yeast pleiotropic drug resistance network.
Multidrug resistance (MDR) mediated by broad specificity transporters is one of the most important strategies used by pathogens… (More)
Is this relevant?
Highly Cited
1995
Highly Cited
1995
EmrR is a negative regulator of the Escherichia coli multidrug resistance pump EmrAB.
The emrAB locus of Escherichia coli encodes a multidrug resistance pump that protects the cell from several chemically unrelated… (More)
  • table 1
  • figure 1
  • figure 2
  • table 2
  • figure 3
Is this relevant?
1979
1979
New antiarrhythmic agents. 1. Primary alpha-amino anilides.
Thirty-two alpha-amino anilides with various substituents in the aromatic ring and in the alpha position are described. Their… (More)
Is this relevant?