1
|
Retracted
SphK1 regulates proinflammatory responses associated with endotoxin and polymicrobial sepsis.
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Science
|
2010
|
3.63
|
2
|
Synthesis and evaluation of sphingosine analogues as inhibitors of sphingosine kinases.
|
J Med Chem
|
2009
|
1.08
|
3
|
CdpA is a Burkholderia pseudomallei cyclic di-GMP phosphodiesterase involved in autoaggregation, flagellum synthesis, motility, biofilm formation, cell invasion, and cytotoxicity.
|
Infect Immun
|
2010
|
1.04
|
4
|
Synthesis and biological evaluation of polyenylpyrrole derivatives as anticancer agents acting through caspases-dependent apoptosis.
|
J Med Chem
|
2010
|
0.99
|
5
|
Solid-phase synthesis of 3,4-dihydro-1H-pyrimidine-2-ones using sodium benzenesulfinate as a traceless linker.
|
J Comb Chem
|
2005
|
0.91
|
6
|
Traceless solid-phase synthesis and biological evaluation of purine analogs as inhibitors of multidrug resistance protein 4.
|
J Comb Chem
|
2007
|
0.87
|
7
|
Traceless solid-phase synthesis of substituted xanthines.
|
J Comb Chem
|
2006
|
0.85
|
8
|
A facile solid-phase synthesis of 1,2,4,5-tetrasubstituted imidazoles using sodium benzenesulfinate as a traceless linker.
|
J Comb Chem
|
2005
|
0.83
|
9
|
Synthesis and disulfide bond connectivity-activity studies of a kalata B1-inspired cyclopeptide against dengue NS2B-NS3 protease.
|
Bioorg Med Chem
|
2009
|
0.82
|
10
|
Clinical and therapeutic relevance of PIM1 kinase in gastric cancer.
|
Gastric Cancer
|
2011
|
0.81
|
11
|
Polyenylpyrrole derivatives inhibit NLRP3 inflammasome activation and inflammatory mediator expression by reducing reactive oxygen species production and mitogen-activated protein kinase activation.
|
PLoS One
|
2013
|
0.78
|
12
|
Synthesis and in vitro evaluation of West Nile virus protease inhibitors based on the 2-{6-[2-(5-phenyl-4H-{1,2,4]triazol-3-ylsulfanyl)acetylamino]benzothiazol-2-ylsulfanyl}acetamide scaffold.
|
ChemMedChem
|
2013
|
0.78
|
13
|
Synthesis of pyrazolo[5,1-d][1,2,3,5]tetrazine-4(3H)-ones.
|
J Comb Chem
|
2010
|
0.78
|
14
|
Synthesis and in vitro evaluation of West Nile virus protease inhibitors based on the 1,3,4,5-tetrasubstituted 1H-pyrrol-2(5H)-one scaffold.
|
ChemMedChem
|
2013
|
0.78
|
15
|
Discovery, synthesis, and in vitro evaluation of West Nile virus protease inhibitors based on the 9,10-dihydro-3H,4aH-1,3,9,10a-tetraazaphenanthren-4-one scaffold.
|
ChemMedChem
|
2012
|
0.77
|
16
|
Fluorous oxime palladacycle: a precatalyst for carbon-carbon coupling reactions in aqueous and organic medium.
|
J Org Chem
|
2012
|
0.77
|
17
|
Specificity and inhibitory mechanism of andrographolide and its analogues as antiasthma agents on NF-κB p50.
|
J Nat Prod
|
2015
|
0.77
|
18
|
Synthesis of cyclic di-nucleotidic acids as potential inhibitors targeting diguanylate cyclase.
|
Bioorg Med Chem
|
2010
|
0.76
|
19
|
Solid-phase synthesis of pyrazolines and isoxazolines with sodium benzenesulfinate as a traceless linker.
|
Org Lett
|
2003
|
0.76
|
20
|
Generation of reactive oxygen species by polyenylpyrroles derivatives causes DNA damage leading to G2/M arrest and apoptosis in human oral squamous cell carcinoma cells.
|
PLoS One
|
2013
|
0.76
|
21
|
Traceless solid-phase synthesis of heteroannulated 1,3-oxazin-6-ones.
|
J Comb Chem
|
2009
|
0.75
|
22
|
Hydrogen peroxide enhances enterokinase-catalysed proteolytic cleavage of fusion protein.
|
Recent Pat Biotechnol
|
2008
|
0.75
|
23
|
Traceless solid-phase synthesis of N1,N7-disubstituted purines.
|
J Comb Chem
|
2005
|
0.75
|
24
|
[3+2] cycloaddition reactions in the solid-phase synthesis of 1,2,3-triazoles.
|
Org Lett
|
2006
|
0.75
|
25
|
[3 + 2] Cycloaddition reactions in the synthesis of triazolo[4,5-b]pyridin-5-ones and pyrrolo[3,4-b]pyridin-2-ones.
|
J Comb Chem
|
2008
|
0.75
|
26
|
Allylic and benzylic sp3 C-H oxidation in water.
|
Org Biomol Chem
|
2014
|
0.75
|
27
|
Microwave-assisted synthesis of substituted 2-(benzylthio)imidazo[1,2a]pyrimidin-5-ones.
|
J Comb Chem
|
2010
|
0.75
|
28
|
Regiospecific solid-phase strategy to N7-substituted purines and its application to 8-azapurines and [I]-condensed purines.
|
J Comb Chem
|
2007
|
0.75
|
29
|
An efficient solid-phase synthesis of 3-substituted and 3,3-disubstituted 1,2-dialkylpyrazolidine-3,5-diones.
|
Org Biomol Chem
|
2008
|
0.75
|
30
|
Synthesis of 2,4-disubstituted 5-aminoimidazoles using microwave irradiation.
|
J Comb Chem
|
2006
|
0.75
|
31
|
Traceless solid-phase synthesis of nitrogen-containing heterocycles and their biological evaluations as inhibitors of neuronal sodium channels.
|
J Comb Chem
|
2004
|
0.75
|
32
|
An efficient and expeditious synthesis of di- and monosubstituted 2-aminoimidazoles.
|
J Comb Chem
|
2007
|
0.75
|
33
|
Traceless solid-phase synthesis of 6-amino- and 6-hydroxyimino-1,3,5-triazine-2,4-diones and 1,3,5-triazine-2,4,6-triones.
|
J Comb Chem
|
2009
|
0.75
|
34
|
A versatile thiouronium-based solid-phase synthesis of 1,3,5-triazines.
|
Chemistry
|
2011
|
0.75
|
35
|
Synthesis and the biological evaluation of 2-benzenesulfonylalkyl-5-substituted-sulfanyl-[1,3,4]-oxadiazoles as potential anti-hepatitis B virus agents.
|
Antiviral Res
|
2006
|
0.75
|
36
|
A highly efficient solid-phase synthesis of 1,3-substituted xanthines.
|
J Comb Chem
|
2005
|
0.75
|
37
|
Solid-phase synthesis of imidazo[1,2-a]pyridine using sodium benzenesulfinate as a traceless linker.
|
Org Lett
|
2002
|
0.75
|