PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
30343052-8	2019	The effects induced by adhesion substrates were inhibited by AG82 (Tyrphostin 25) and herbimycin A, indicating their dependence on the activation of both the EGF receptor and the tyrosine kinase c-src.	Tyrphostins	67-77	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	195-200	
11493667-6	2001	Moreover, treatment of wild-type cells with tyrphostin AG1007, which inhibits both pp60(c-src) and FAK activity, induced accumulation of tensin in peripheral focal adhesions.	Tyrphostins	44-54	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	88-93	
20499167-4	2010	Our results show that 2.5 microM tyrphostin, 1.0 microM PP1, 4.0 microM U73122, 1.0 microM JNK inhibitor V and 2.0 microM rottlerin blocked the ouabain effect indicating an involvement of receptors for EGF, Src, PLC, JNK and PKC delta respectively.	Tyrphostins	33-43	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	207-210	
16341234-6	2006	We also show that BzATP and ATP activate ERK1/2 by two different pathways since ERK1/2 activation by BzATP, but not by ATP, is blocked by the tryrosine kinase inhibitor, genistein, and the Src protein kinase inhibitor, tyrphostin.	Tyrphostins	219-229	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	189-192	
21697238-6	2011	Tyrphostin AG1478 and PP2, inhibitors of EGFR and Src, respectively, blocked ouabain-dependent ADPKD cell proliferation.	Tyrphostins	0-10	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	50-53	
21887406-10	2011	The obtained data indicate that all tree investigated tyrphostins (AG1024, SU1498 and A23) inhibit signal transmission by Akt (PKB), ERK(1/2), Src and STAT in a similar manner.	Tyrphostins	54-65	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	143-146	
12435806-5	2002	HU-210-induced ERK activation was inhibited by tyrphostin AG1478 and PP2, widely employed inhibitors of the epidermal growth factor receptor (EGF(R)) and the Src family of cytosolic tyrosine kinases, respectively.	Tyrphostins	47-57	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	158-161	
7487083-1	1995	We recently reported that tyrphostin 23 (3,4-dihydroxybenzylidene malononitrile) is unstable in solution and that some of the degradation products are better inhibitors of the tyrosine kinase activity of Src and the EGF-receptor kinase than the parent compound itself (Ramdas et al., Cancer Res.	Tyrphostins	26-36	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	204-207	
9736460-0	1998	Opposing effects of cyclosporin A and tyrphostin AG-1478 indicate a role for Src protein in the cellular control of mineralization.	Tyrphostins	38-48	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	77-80	
8789407-3	1995	In both membrane and cytosolic fractions of porcine coronary artery, we detected src-related tyrosine kinase activity that could be inhibited by both genistein and tyrphostin.	Tyrphostins	164-174	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	81-84	
8789407-5	1995	Protein in both peaks exhibited Western blot cross-reactivity with anti-src antibodies and contained tyrosine kinase activity that was inhibited by genistein and tyrphostin.	Tyrphostins	162-172	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	72-75	
8789407-7	1995	However, because of the comparatively low sensitivity of the isolated src kinase activity towards genistein and tyrphostin, compared with the much higher sensitivity of the contractile response to these inhibitors, a direct role for c-rsc in the regulation of contractions elicited by agonists such as angiotensin II and arginine vasopressin cannot yet be assigned.	Tyrphostins	112-122	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	70-73