Reaction Details |
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Target | Chymase |
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Ligand | BDBM50135493 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_49439 |
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IC50 | 82±n/a nM |
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Citation | Masaki, H; Mizuno, Y; Tatui, A; Murakami, A; Koide, Y; Satoh, S; Takahashi, A Structure-activity relationship of benzo[b]thiophene-2-sulfonamide derivatives as novel human chymase inhibitors. Bioorg Med Chem Lett13:4085-8 (2003) [PubMed] |
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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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BDBM50135493 |
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n/a |
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Name | BDBM50135493 |
Synonyms: | 5-Fluoro-3-methyl-benzo[b]thiophene-2-sulfonic acid (4-acetyl-2-methanesulfonyl-phenyl)-amide | CHEMBL335613 |
Type | Small organic molecule |
Emp. Form. | C18H16FNO5S3 |
Mol. Mass. | 441.517 |
SMILES | CC(=O)c1ccc(NS(=O)(=O)c2sc3ccc(F)cc3c2C)c(c1)S(C)(=O)=O |
Structure |
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