Reaction Details |
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Target | Chymase |
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Ligand | BDBM50210741 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_455468 (CHEMBL886244) |
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IC50 | 470±n/a nM |
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Citation | Maruoka, H; Muto, T; Tanaka, T; Imajo, S; Tomimori, Y; Fukuda, Y; Nakatsuka, T Development of 6-benzyl substituted 4-aminocarbonyl-1,4-diazepane-2,5-diones as orally active human chymase inhibitors. Bioorg Med Chem Lett17:3435-9 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Chymase |
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Name: | Chymase |
Synonyms: | Alpha-chymase | CMA1 | CMA1_HUMAN | CYH | CYM | Chymase precursor | Mast cell protease I |
Type: | Enzyme |
Mol. Mass.: | 27340.12 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 247 |
Sequence: | MLLLPLPLLLFLLCSRAEAGEIIGGTECKPHSRPYMAYLEIVTSNGPSKFCGGFLIRRNF
VLTAAHCAGRSITVTLGAHNITEEEDTWQKLEVIKQFRHPKYNTSTLHHDIMLLKLKEKA
SLTLAVGTLPFPSQFNFVPPGRMCRVAGWGRTGVLKPGSDTLQEVKLRLMDPQACSHFRD
FDHNLQLCVGNPRKTKSAFKGDSGGPLLCAGVAQGIVSYGRSDAKPPAVFTRISHYRPWI
NQILQAN
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BDBM50210741 |
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n/a |
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Name | BDBM50210741 |
Synonyms: | 4-(1-(6-(5-chloro-2-methoxybenzyl)-2,5-dioxo-1,4-diazepane-4-carboxamido)propyl)benzoic acid | CHEMBL247779 |
Type | Small organic molecule |
Emp. Form. | C24H26ClN3O6 |
Mol. Mass. | 487.933 |
SMILES | CCC(NC(=O)N1CC(=O)NCC(Cc2cc(Cl)ccc2OC)C1=O)c1ccc(cc1)C(O)=O |
Structure |
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