PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 19100119-10 2008 The expressions of p-JAK2 and p-STAT3 as well as the expression of AGT mRNA and c-fos mRNA significantly activated by CT-1, which could be inhibited by SIM or Janus Kinase-selective inhibitor AG490. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 192-197 angiotensinogen Rattus norvegicus 67-70 30412649-11 2019 Moreover, the p38 mitogen-activated protein kinase (MAPK) inhibitor SB203580, the c-Jun N-terminal kinase (JNK) inhibitor SP600125 and the Janus-activated kinase (JAK)2 inhibitor AG490 suppressed Ang II-induced differentiation of BM-MSCs into keratinocytes. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 179-184 angiotensinogen Rattus norvegicus 196-202 9299374-10 1997 Selective inhibition of Jak2 kinase with AG-490 blocked formation of angiotensin II induced SIF complexes, suggesting that Jak2 kinase is required for cardiomyocyte SIF induction. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 41-47 angiotensinogen Rattus norvegicus 69-83 32620936-10 2021 Pretreatment of NRCMs with the Jak2 inhibitor AG490 (10 microM) blocked Ang II-induced reduction in GJA1-20k expression and Cx43 gap junction formation; knockdown of Jak2 in NRCMs significantly lessened Ang II-induced cardiomyocyte hypertrophy and normalized GJA1-20k expression and Cx43 gap junction formation. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 46-51 angiotensinogen Rattus norvegicus 72-78 32620936-10 2021 Pretreatment of NRCMs with the Jak2 inhibitor AG490 (10 microM) blocked Ang II-induced reduction in GJA1-20k expression and Cx43 gap junction formation; knockdown of Jak2 in NRCMs significantly lessened Ang II-induced cardiomyocyte hypertrophy and normalized GJA1-20k expression and Cx43 gap junction formation. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 46-51 angiotensinogen Rattus norvegicus 203-209 25088002-10 2014 Pretreatment of the cells with AG490, a JAK2 inhibitor, markedly inhibited Ang II-induced STAT3 phosphorylation on Tyr705 and fibronectin expression. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 31-36 angiotensinogen Rattus norvegicus 75-81 24058756-5 2012 The Ang II-mediated phosphorylation of both JAK2 and STAT3 was blocked by AG490, a selective JAK2 inhibitor. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 74-79 angiotensinogen Rattus norvegicus 4-10 15770649-5 2005 We also found that AGE (150 microg/ml) increased angiotensinogen protein at 2 days, which was attenuated by AG-490 (a JAK2 inhibitor). alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 108-114 angiotensinogen Rattus norvegicus 49-64 15770649-9 2005 AG-490 and CTGF antisense (but not sense) oligodeoxynucleotide (ODN) attenuated Ang II (10(-7)M) and AGE-induced mitogenesis and type I collagen production at 3 and 7 days, respectively. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 0-6 angiotensinogen Rattus norvegicus 80-86 10884366-9 2000 Additionally, a Jak2 inhibitor, AG490, blocked the Ang II-induced Stat3 phosphorylation. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 32-37 angiotensinogen Rattus norvegicus 51-57 9732408-9 1998 The nonflavone tyrosine kinase inhibitor tyrphostin B42 (30 microM) reduced Ang II-induced maximal contraction (to 11.2% control) but, unlike the other tyrosine kinase inhibitors, also reduced KCl-induced contraction (to 55.2% control), indicating a probable nonselectivity of tyrphostin B42. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 41-55 angiotensinogen Rattus norvegicus 76-82 9602424-13 1998 Selective inhibition of Jak2 kinase with AG-490 blocked formation of prolactin-inducing factor (PIF) complexes by Ang II, suggesting that Jak2 kinase was required for the tyrosine phosphorylation of Stat5 in cardiac myocytes. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 41-47 angiotensinogen Rattus norvegicus 114-120