PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 10614779-4 1999 Although only hydroxamate matrix metalloproteinase (MMP) inhibitors inhibited the basal processing and release of TNF-alpha, the PMA-induced processing and release of TNF-alpha were inhibited not only by MMP inhibitors but also by 1,10-phenanthroline, 3,4-dichloroisocoumarin (3,4-DCI), iodoacetamide, and Nalpha-p-tosyl-L-phenylalanine chloromethyl ketone (TPCK). 1,10-phenanthroline 231-250 tumor necrosis factor Homo sapiens 167-176 10614779-5 1999 Hydroxamate MMP inhibitors and 1,10-phenanthroline inhibited the processing of TNF-alpha on the cell surface, whereas 3,4-DCI, iodoacetamide, and TPCK inhibited the transport of TNF-alpha to the cell surface. 1,10-phenanthroline 31-50 tumor necrosis factor Homo sapiens 79-88 7569774-5 1995 Furthermore, 1,10-phenanthroline also reduced PMA-induced down-regulation of TNF-receptors in both cell lines as judged by TNF-binding to cells. 1,10-phenanthroline 13-32 tumor necrosis factor Homo sapiens 77-80 10090924-6 1999 The downmodulation of CXCR1 and CXCR2 by LPS and TNF-alpha was most dramatically inhibited by metalloproteinase inhibitors; 1, 10-phenanthroline and EDTA significantly attenuated LPS- and TNF-alpha-induced loss of CXCR1 and CXCR2 cell surface expression. 1,10-phenanthroline 124-144 tumor necrosis factor Homo sapiens 188-197 10090924-8 1999 In addition, while treatment of neutrophils with LPS and TNF-alpha inhibited IL-8 receptor-mediated calcium mobilization and IL-8-directed neutrophil chemotaxis, both 1, 10-phenanthroline and EDTA blocked these inhibitory processes. 1,10-phenanthroline 167-187 tumor necrosis factor Homo sapiens 57-66 7569774-5 1995 Furthermore, 1,10-phenanthroline also reduced PMA-induced down-regulation of TNF-receptors in both cell lines as judged by TNF-binding to cells. 1,10-phenanthroline 13-32 tumor necrosis factor Homo sapiens 123-126 7569774-6 1995 Reduced down-regulation and TNF-receptor shedding by 1,10-phenanthroline was reversed by Zn2+, indicating involvement of a Zn(2+)-dependent metalloprotease. 1,10-phenanthroline 53-72 tumor necrosis factor Homo sapiens 28-31 7962141-7 1994 It was discovered that cupric o-phenanthroline markedly potentiated the effects of TNF on the resistant CEM-SS cells leading to cell death. 1,10-phenanthroline 30-46 tumor necrosis factor Homo sapiens 83-86 25414128-3 2017 We found that O-phenanthroline reduced the expression of MMP3 and MMP13 mRNA levels during chondrogenic differentiation of human chondrocytes (hChs), as well as after TNFalpha/IL-1beta exposure in an explant model. 1,10-phenanthroline 14-30 tumor necrosis factor Homo sapiens 167-175 25414128-4 2017 Interestingly, O-phenanthroline significantly inhibited matrix degradation in a TNFalpha/IL-1beta-dependent model of cartilage degeneration when compared to control and natural hypoxia (2.5% O2 ). 1,10-phenanthroline 15-31 tumor necrosis factor Homo sapiens 80-88