Reaction Details |
| Report a problem with these data |
Target | fMet-Leu-Phe receptor |
---|
Ligand | BDBM50211790 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_438742 (CHEMBL887899) |
---|
Ki | >10000±n/a nM |
---|
Citation | Bruno, O; Brullo, C; Bondavalli, F; Ranise, A; Schenone, S; Falzarano, MS; Varani, K; Spisani, S 2-Phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole derivatives: new potent inhibitors of fMLP-induced neutrophil chemotaxis. Bioorg Med Chem Lett17:3696-701 (2007) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
fMet-Leu-Phe receptor |
---|
Name: | fMet-Leu-Phe receptor |
Synonyms: | FPR | FPR1 | FPR1_HUMAN | Formyl peptide Receptor | N-formyl peptide receptor 1 | N-formylpeptide chemoattractant receptor | fMLP receptor | fMet-Leu-Phe receptor | formyl peptide receptor 1 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 38456.14 |
Organism: | Homo sapiens (Human) |
Description: | gi_4503779 |
Residue: | 350 |
Sequence: | METNSSLPTNISGGTPAVSAGYLFLDIITYLVFAVTFVLGVLGNGLVIWVAGFRMTHTVT
TISYLNLAVADFCFTSTLPFFMVRKAMGGHWPFGWFLCKFVFTIVDINLFGSVFLIALIA
LDRCVCVLHPVWTQNHRTVSLAKKVIIGPWVMALLLTLPVIIRVTTVPGKTGTVACTFNF
SPWTNDPKERINVAVAMLTVRGIIRFIIGFSAPMSIVAVSYGLIATKIHKQGLIKSSRPL
RVLSFVAAAFFLCWSPYQVVALIATVRIRELLQGMYKEIGIAVDVTSALAFFNSCLNPML
YVFMGQDFRERLIHALPASLERALTEDSTQTSDTATNSTLPSAEVELQAK
|
|
|
BDBM50211790 |
---|
n/a |
---|
Name | BDBM50211790 |
Synonyms: | (2-phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazol-7-yl)(pyrrolidin-1-yl)methanone | CHEMBL438108 |
Type | Small organic molecule |
Emp. Form. | C16H18N4O |
Mol. Mass. | 282.3403 |
SMILES | O=C(N1CCCC1)c1cnn2CC(Nc12)c1ccccc1 |w:12.17| |
Structure |
|