PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 21779957-3 2012 Pretreatment with potassium cyanide (KCN, a cytochrome pathway inhibitor) greatly increased CN-resistant R and reduced reactive oxygen species (ROS) formation, while application of salicylhydroxamic acid (SHAM, an AOX inhibitor) blocked the AOX activity and enhanced the production of ROS in the plants. salicylhydroxamic acid 181-203 acyl-CoA oxidase 1 Homo sapiens 241-244 22429403-4 2012 The inhibition of the AOX pathway by salicylhydroxamic acid (SHAM) caused the over-reduction of the photosystem I (PSI) acceptor side, as indicated by the increases in the extent of reduction of P700+. salicylhydroxamic acid 37-59 acyl-CoA oxidase 1 Homo sapiens 22-25 20059739-6 2010 Upon restriction of AOX pathway using salicylhydroxamic acid (SHAM), the observed decrease in NaHCO(3)-dependent O(2) evolution or p-benzoquinone (BQ)-dependent O(2) evolution [indicator of photosystem II (PSII) activity] and the increase in total cellular levels of pyruvate and malate were further aggravated/promoted under HL. salicylhydroxamic acid 38-60 acyl-CoA oxidase 1 Homo sapiens 20-23 9724695-0 1998 Cyanide restores N gene-mediated resistance to tobacco mosaic virus in transgenic tobacco expressing salicylic acid hydroxylase Salicylhydroxamic acid (SHAM), an inhibitor of alternative oxidase (AOX), blocks salicylic acid-induced resistance to tobacco mosaic virus (TMV) but does not inhibit pathogenesis-related PR-1 protein synthesis or resistance to fungal and bacterial pathogens. salicylhydroxamic acid 129-151 acyl-CoA oxidase 1 Homo sapiens 197-200 19958137-5 2010 Salicylhydroxamic acid (SHAM, an AOX inhibitor) pretreatment reduced the DEA/NO-induced cyanide-resistant respiration and partially compromised induced resistance to TMV. salicylhydroxamic acid 0-22 acyl-CoA oxidase 1 Homo sapiens 33-36 11351100-10 2001 Inhibition of the AOX (with salicylhydroxamic acid) decreases respiration rates less than the activity present before inhibition (i.e. measured with the 18O-fractionation technique). salicylhydroxamic acid 28-50 acyl-CoA oxidase 1 Homo sapiens 18-21 31795459-6 2019 However, this mitigating effect was aggravated by salicylhydroxamic acid (SHAM, an AOX inhibitor), suggesting that AP contributes to NO-enhanced Cd stress tolerance. salicylhydroxamic acid 50-72 acyl-CoA oxidase 1 Homo sapiens 83-86 31795459-6 2019 However, this mitigating effect was aggravated by salicylhydroxamic acid (SHAM, an AOX inhibitor), suggesting that AP contributes to NO-enhanced Cd stress tolerance. salicylhydroxamic acid 74-78 acyl-CoA oxidase 1 Homo sapiens 83-86