PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8831515-10	1996	Stretch-induced changes in levels of Ang II receptors were inhibited by genistein but not by H-7, staurosporin, and protein kinase C depletion or by BAPTA-AM.	1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine	93-96	angiotensinogen	Rattus norvegicus	37-43	
15694920-9	2005	Pressure application of H-7 alone decreased the basal firing activity of angiotensin II-sensitive neurons in SHR but not in WKY.	1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine	24-27	angiotensinogen	Rattus norvegicus	73-87	
10882187-6	2000	Pretreatment with 10(-6) M of PKC inhibitor, 1-(5-isoquinolinesulfonyl-methyl) piperazine (H7), blocked Ang II-induced hypertrophy and PGF2alpha release.	1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine	91-93	angiotensinogen	Rattus norvegicus	104-110	
11841996-4	2002	ANG II-induced contraction of rat IAS smooth muscle and SMC was attenuated by tyrosine kinase inhibitors genistein and tyrphostin, protein kinase C (PKC) inhibitor H-7, Ca(2+) channel blocker nicardipine, Rho kinase inhibitor Y-27632 or p(44/42) mitogen-activating protein kinase (MAPK(44/42)) inhibitor PD-98059.	1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine	164-167	angiotensinogen	Rattus norvegicus	0-6	
11841996-5	2002	Combinations of nicardipine and H-7, Y-27632, and PD-98059 caused further attenuation of the ANG II effects.	1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine	32-35	angiotensinogen	Rattus norvegicus	93-99	
8632699-6	1996	We observed that PMA (0.1 microM) stimulated ANP release whereas H-7 (10 microM), an inhibitor of PKC in the presence of Ang II, prevented ANP increase.	1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine	65-68	angiotensinogen	Rattus norvegicus	121-127