Reaction Details |
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Target | fMet-Leu-Phe receptor |
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Ligand | BDBM50211798 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_438742 (CHEMBL887899) |
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Ki | >10000±n/a nM |
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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 |
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More Info.: | Get all data from this article, Assay Method |
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fMet-Leu-Phe receptor |
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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
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BDBM50211798 |
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n/a |
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Name | BDBM50211798 |
Synonyms: | 2-phenyl-2,3-dihydro-1H-imidazo[1,2-b]pyrazole-7-carboxylic acid | CHEMBL230049 |
Type | Small organic molecule |
Emp. Form. | C12H11N3O2 |
Mol. Mass. | 229.2346 |
SMILES | OC(=O)c1cnn2CC(Nc12)c1ccccc1 |w:8.12| |
Structure |
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