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E 3810

Known as: E-3810, E3810 
 
National Institutes of Health

Papers overview

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2015
2015
Human fibroblast growth factor receptors (FGFRs) 1-4 are a family of receptor tyrosine kinases that can serve as drivers of… Expand
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2013
2013
E-3810 is a novel small molecule that inhibits VEGF receptor-1, -2, and -3 and fibroblast growth factor receptor-1 tyrosine… Expand
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Highly Cited
2011
Highly Cited
2011
Tumor angiogenesis is a degenerate process regulated by a complex network of proangiogenic factors. Existing antiangiogenic drugs… Expand
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Highly Cited
1998
Highly Cited
1998
BACKGROUND Rabeprazole (LY307640, E3810) is a new, potent, proton pump inhibitor. A single daily 20 mg dose significantly… Expand
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1995
1995
OBJECTIVE To compare the interaction potential of E3810, [(+/-)-sodium 2-[[4-(3-methoxpropoxy)-3-methylpyridin-2-yl… Expand
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Highly Cited
1995
Highly Cited
1995
We studied the kinetic disposition and metabolism of E3810 [(+/-)-sodium 2-[[4-(3-methoxypropoxy)-3-methylpyridin-2-yl… Expand
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1995
1995
Helicobacter pylori infection is causally related to atrophic gastritis, and it may also be associated with peptic ulcer and… Expand
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1994
1994
E3810 is a new H+,K(+)-ATPase inhibitor with a substituted benzimidazole, which is under clinical investigation for peptic ulcer… Expand
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1991
1991
A substituted benzimidazole ([4-(3-methoxypropoxy)-3-methylpyridine-2-yl]methylsulfinyl)- 1H-benzimidazole sodium salt (E3810… Expand
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1990
1990
The half maximal inhibitory concentrations (IC50) of substituted benzimidazoles for the H+, K(+)-ATPase in hog gastric vesicles… Expand
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