Reaction Details | |||
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Target | Cathepsin G | ||
Ligand | BDBM21737 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_498939 (CHEMBL976246) | ||
Ki | 0.15±n/a nM | ||
Citation | Łegowska, A; Debowski, D; Lesner, A; Wysocka, M; Rolka, K Introduction of non-natural amino acid residues into the substrate-specific P1 position of trypsin inhibitor SFTI-1 yields potent chymotrypsin and cathepsin G inhibitors. Bioorg Med Chem17:3302-7 (2009) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Cathepsin G | |||
Name: | Cathepsin G | ||
Synonyms: | CATG_HUMAN | CG | CTSG | ||
Type: | PROTEIN | ||
Mol. Mass.: | 28860.08 | ||
Organism: | Homo sapiens (Human) | ||
Description: | ChEMBL_1469016 | ||
Residue: | 255 | ||
Sequence: |
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BDBM21737 | |||
n/a | |||
Name | BDBM21737 | ||
Synonyms: | 2-[(1R,4S,7S,13S,19S,22S,25S,28S,31R,34S,40S,43S,49S)-25-(4-aminobutyl)-49-benzyl-4,19-bis[(2S)-butan-2-yl]-34-(3-carbamimidamidopropyl)-28-[(1R)-1-hydroxyethyl]-22-(hydroxymethyl)-3,6,12,18,21,24,27,30,33,36,39,42,48,51-tetradecaoxo-53,54-dithia-2,5,11,17,20,23,26,29,32,35,38,41,47,50-tetradecaazapentacyclo[29.20.4.0^{7,11}.0^{13,17}.0^{43,47}]pentapentacontan-40-yl]acetic acid | CHEMBL453539 | Sunflower trypsin inhibitor-1(SFTI-1) | US20240010684, Ref. No 2 | ||
Type | bicyclic peptide | ||
Emp. Form. | C67H104N18O18S2 | ||
Mol. Mass. | 1513.782 | ||
SMILES | [#6]-[#6]-[#6@H](-[#6])-[#6@@H]-1-[#7]-[#6](=O)-[#6@@H]-2-[#6]-[#6]-[#6]-[#7]-2-[#6](=O)-[#6@@H]-2-[#6]-[#6]-[#6]-[#7]-2-[#6](=O)-[#6@@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#8])-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]-[#6]-[#7])-[#7]-[#6](=O)-[#6@@H](-[#7]-[#6](=O)-[#6@@H]-2-[#6]-[#16]-[#16]-[#6]-[#6@H](-[#7]-[#6]-1=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-c1ccccc1)-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@H]-1-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6](-[#8])=O)-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-2)-[#6@@H](-[#6])-[#8])-[#6@@H](-[#6])-[#6]-[#6] |r| | ||
Structure |