PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 10447750-5 1999 Inhibition of the antigen presenting capacity by piceatannol, a protein tyrosine kinase (PTK) syk inhibitor, indicates that this is an active process resulting from immunoglobulin E (IgE)-antigen-FcepsilonRI engagement which involves tyrosines found in the immunoreceptor tyrosine-based activation motif (ITAM) embedded in the cytoplasmic tail of the FcepsilonRI beta and gamma chains. 3,3',4,5'-tetrahydroxystilbene 49-60 spleen tyrosine kinase Mus musculus 94-97 10754332-9 2000 Although piceatannol, a reportedly selective inhibitor of Syk, also prevented degranulation and activation of p38 MAPK, no fMLP-induced phosphorylation of Syk could be observed, raising doubts about the specificity of the inhibitor. 3,3',4,5'-tetrahydroxystilbene 9-20 spleen tyrosine kinase Mus musculus 58-61 9732296-4 1998 The Syk inhibitor piceatannol blocks the Syk homologue ZAP-70, which is expressed by TAM2D2 cells, with the same dose dependence as the inhibition of invasion. 3,3',4,5'-tetrahydroxystilbene 18-29 spleen tyrosine kinase Mus musculus 4-7 9732296-4 1998 The Syk inhibitor piceatannol blocks the Syk homologue ZAP-70, which is expressed by TAM2D2 cells, with the same dose dependence as the inhibition of invasion. 3,3',4,5'-tetrahydroxystilbene 18-29 spleen tyrosine kinase Mus musculus 41-44 9396765-7 1997 Pharmacologic exposure to piceatannol, a known Syk family kinase inhibitor, inhibits natural cytotoxicity. 3,3',4,5'-tetrahydroxystilbene 26-37 spleen tyrosine kinase Mus musculus 47-50 35230826-9 2022 Targeting this subset with ANP loaded with the drug piceatannol, a spleen tyrosine kinase (Syk) inhibitor, mitigated the effects of polymicrobial sepsis by reducing tissue inflammation while fully preserving neutrophilic host-defense function. 3,3',4,5'-tetrahydroxystilbene 52-63 spleen tyrosine kinase Mus musculus 67-89 35230826-9 2022 Targeting this subset with ANP loaded with the drug piceatannol, a spleen tyrosine kinase (Syk) inhibitor, mitigated the effects of polymicrobial sepsis by reducing tissue inflammation while fully preserving neutrophilic host-defense function. 3,3',4,5'-tetrahydroxystilbene 52-63 spleen tyrosine kinase Mus musculus 91-94 19017976-4 2008 Pretreatment of mDC with the Syk inhibitor piceatannol blocked B7-DC XAb-induced Ag uptake with a concomitant loss of tumor protection in mice. 3,3',4,5'-tetrahydroxystilbene 43-54 spleen tyrosine kinase Mus musculus 29-32 28680194-2 2017 Indeed, we found that overexpression of myeloid differentiation primary response gene 88 (MyD88), an adaptor molecule that drives TLR signaling, induced IRAK1 expression and that piceatannol, a Syk inhibitor, successfully suppressed the MyD88-dependent upregulation of IRAK1 under LPS treatment conditions. 3,3',4,5'-tetrahydroxystilbene 179-190 spleen tyrosine kinase Mus musculus 194-197 28680194-4 2017 According to our measurements of IRAK1 mRNA levels, the transcriptional upregulation of IRAK1 was induced by LPS treatment between 4 and 60 min, and this can be suppressed in Syk knockout cells, providing an effect similar that that seen under piceatannol treatment. 3,3',4,5'-tetrahydroxystilbene 244-255 spleen tyrosine kinase Mus musculus 175-178 27186801-1 2016 Piceatannol is a polyphenolic analog of resveratrol that selectively inhibits the non-receptor tyrosine kinase-Syk. 3,3',4,5'-tetrahydroxystilbene 0-11 spleen tyrosine kinase Mus musculus 111-114 24212132-5 2013 We treated mice with piceatannol, a Syk inhibitor, and consequently the infarct volume and swelling were suppressed by piceatannol. 3,3',4,5'-tetrahydroxystilbene 21-32 spleen tyrosine kinase Mus musculus 36-39 24212132-5 2013 We treated mice with piceatannol, a Syk inhibitor, and consequently the infarct volume and swelling were suppressed by piceatannol. 3,3',4,5'-tetrahydroxystilbene 119-130 spleen tyrosine kinase Mus musculus 36-39 24212132-6 2013 The levels of phospho-Syk, MMP9 and ICAM-1 were downregulated, and the level of Claudin5 was uplegurated in piceatannol-treated groups. 3,3',4,5'-tetrahydroxystilbene 108-119 spleen tyrosine kinase Mus musculus 22-25 16751367-7 2006 Pretreatment of the cells with Src-family or Syk-family selective tyrosine kinase inhibitors, PP2 or piceatannol, respectively, inhibited the formation of microtubules and reduced the amount of tyrosine phosphorylated proteins in gamma-tubulin complexes, suggesting that Src and Syk family kinases are involved in the initial stages of microtubule formation. 3,3',4,5'-tetrahydroxystilbene 101-112 spleen tyrosine kinase Mus musculus 45-48 16751367-7 2006 Pretreatment of the cells with Src-family or Syk-family selective tyrosine kinase inhibitors, PP2 or piceatannol, respectively, inhibited the formation of microtubules and reduced the amount of tyrosine phosphorylated proteins in gamma-tubulin complexes, suggesting that Src and Syk family kinases are involved in the initial stages of microtubule formation. 3,3',4,5'-tetrahydroxystilbene 101-112 spleen tyrosine kinase Mus musculus 279-282