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TargetChymase
LigandBDBM50208239
Substrate/Competitorn/a
Meas. Tech.ChEMBL_429291 (CHEMBL915852)
IC50 66±n/a nM
Citation Greco, MNHawkins, MJPowell, ETAlmond, HRde Garavilla, LHall, JMinor, LKWang, YCorcoran, TWDi Cera, ECantwell, AMSavvides, SNDamiano, BPMaryanoff, BE Discovery of potent, selective, orally active, nonpeptide inhibitors of human mast cell chymase. J Med Chem50:1727-30 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Chymase
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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  Blast E-value cutoff:
BDBM50208239
n/a
NameBDBM50208239
Synonyms:(E)-2-(4-fluorostyrylamino)-1-(5-chlorobenzo[b]thiophen-3-yl)-2-oxoethylphosphonic acid | CHEMBL222952
TypeSmall organic molecule
Emp. Form.C18H14ClFNO4PS
Mol. Mass.425.798
SMILESOP(O)(=O)C(C(=O)NC=Cc1ccc(F)cc1)c1csc2ccc(Cl)cc12 |w:9.9|
Structure
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