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methyl 2,5-dihydroxycinnamate

Known as: 2,4-dihydroxymethylcinnamate, 3-(2,5-Dihydroxyphenyl)-2-propenoic Acid Methyl Ester, Methyl 3-(2,5-dihydroxyphenyl)-2-propenoate 
A cell-permeable analog of erbstatin, a compound isolated from Streptomyces that inhibits the autophosphorylation of epidermal growth factor receptor… 
National Institutes of Health

Related topics

Related topics

6 relations

Narrower (1)

ALX-270-098

Broader (4)

Antineoplastic AgentsCinnamatesCross-Linking ReagentsEnzyme Inhibitors
Receptor Tyrosine Kinase Inhibition

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2002
2002
Synthesis and cytotoxicity of some rigid derivatives of methyl 2,5-Dihydroxycinnamate
Eight rigid compounds designed as esterase-stable analogues of methyl 2,5-dihydroxycin-namate (1) were synthesized. These… 
1998
1998
Regulation of the renal Na–HCO3 cotransporter: IX. Modulation by insulin, epidermal growth factor and carbachol
1997
1997
Protein tyrosine kinase, mitogen-activated protein kinase and protein kinase C are involved in the mitogenic signaling of platelet-activating factor (PAF) in HEC-1A cells.
1997
1997
Inhibition of protein tyrosine kinases or protein kinase C prevents nonspecific killer T lymphocyte-mediated tumoricidal activity.
1996
1996
Cell protein cross-linking by erbstatin and related compounds.
1996
1996
Mechanism of Topoisomerase II Inhibition by Staurosporine and Other Protein Kinase Inhibitors*
Topoisomerase II is an essential enzyme for proliferation of eukaryotic cells. It is also a target for many antineoplastic drugs… 
1995
1995
Alpha 2-adrenoceptor-mediated vasoconstriction requires a tyrosine kinase.
1995
1995
Possible role of protein kinase C in the regulation of intracellular stability of focal adhesion kinase in mouse 3T3 cells
1993
1993
Differentiation of human monoblastic leukemia U937 cells induced by inhibitors of myosin light chain kinase and prevention of differentiation by granulocyte-macrophage colony-stimulating factor.
1991
1991
Induction of morphological change by tyrosine kinase inhibitors in Rous sarcoma virus‐transformed rat kidney cells
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