PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 6212947-1 1982 Part 26: Inhibition of trypsin, plasmin and thrombin by amides of N alpha-arylsulfonylated 2-amino-4-(4-amidino-phenyl) butyric acid and 2-amino-5-amidinophenyl valeric acids (author"s transl)]. Amides 56-62 plasminogen Homo sapiens 32-39 2955429-2 1987 Inhibition of trypsin, plasmin and thrombin by amides of N-alpha-substituted 4-amidinophenylalanine. Amides 47-53 plasminogen Homo sapiens 23-30 6458047-1 1981 Part 25: Inhibition of trypsin, plasmin and thrombin by amides of N alpha-substituted amidinophenylalanines and 3-amidinophenyl-3-aminopropionic acids (author"s transl)]. Amides 56-62 plasminogen Homo sapiens 32-39 6458047-2 1981 Amides of N alpha-substituted 3-amidinophenylalanine are potent inhibitors of the serine proteinases trypsin, plasmin and thrombin. Amides 0-6 plasminogen Homo sapiens 110-117 6458047-4 1981 In contrast, amides of 4-amidinophenylalanine possess weak inhibitory activity towards trypsin and plasmin. Amides 13-19 plasminogen Homo sapiens 99-106 10560742-2 1999 We have explored SAR around the C-terminal amide part for inhibition of uPA, plasmin and trypsin. Amides 43-48 plasminogen Homo sapiens 77-84 8506386-3 1993 After activation of this zymogen to its corresponding form of the serine protease plasmin (MrhPm), this latter enzyme was essentially inactive toward an amide plasmin substrate, most likely from alteration of the spatial relationships of the active-site His-603 to its partners of the catalytic triad, Asp-646 and Ser-741. Amides 153-158 plasminogen Homo sapiens 82-89 3835889-6 1985 The results are shown below: 1) Both activities for decomposition of amide against the specific substrates of plasmin and of P.G.-activator were revealed. Amides 69-74 plasminogen Homo sapiens 110-117 6237371-5 1984 In contrast, amidinoanilides of N alpha-substituted omega-phenyl-alpha-aminoalkylcarboxylic acids are potent inhibitors of trypsin and plasmin, their inhibitory activity approaches that of primary amides of N alpha-substituted omega-amidinophenyl-alpha-aminoalkylcarboxylic acids. Amides 197-203 plasminogen Homo sapiens 135-142 59608-3 1976 The number of active sites of plasmin has been determined through a burst titration of nitroaniline during the presteady-state hydrolysis of an amide substrate (N-alpha-carbobenzoxy-L-arginine-p-nitroanilide). Amides 144-149 plasminogen Homo sapiens 30-37 144444-0 1977 Flourogenic peptide amide substrates for the estimation of plasminogen activators and plasmin. Amides 20-25 plasminogen Homo sapiens 59-66 31618846-7 2019 The test results showed that the most active plasmin inhibitors were palmitoyl peptides, whether in acid or amide form. Amides 108-113 plasminogen Homo sapiens 45-52