Reaction Details |
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Target | C-X-C chemokine receptor type 2 |
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Ligand | BDBM50113636 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_44676 (CHEMBL656549) |
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IC50 | 1200±n/a nM |
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Citation | Cutshall, NS; Kucera, KA; Ursino, R; Latham, J; Ihle, NC Nicotinanilides as inhibitors of neutrophil chemotaxis. Bioorg Med Chem Lett12:1517-20 (2002) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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C-X-C chemokine receptor type 2 |
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Name: | C-X-C chemokine receptor type 2 |
Synonyms: | C-X-C chemokine receptor type 2 (CXCR-2) | C-X-C chemokine receptor type 2 (CXCR2) | CD_antigen=CD182 | CDw128b | CXCR-2 | CXCR2 | CXCR2_HUMAN | Chemokine receptor type 2 (CXCR2) | GRO/MGSA receptor | High affinity interleukin-8 receptor B | IL-8 receptor type 2 | IL-8R B | IL8RB | Interleukin-8 receptor B |
Type: | Protein |
Mol. Mass.: | 40767.88 |
Organism: | Homo sapiens (Human) |
Description: | P25025 |
Residue: | 360 |
Sequence: | MEDFNMESDSFEDFWKGEDLSNYSYSSTLPPFLLDAAPCEPESLEINKYFVVIIYALVFL
LSLLGNSLVMLVILYSRVGRSVTDVYLLNLALADLLFALTLPIWAASKVNGWIFGTFLCK
VVSLLKEVNFYSGILLLACISVDRYLAIVHATRTLTQKRYLVKFICLSIWGLSLLLALPV
LLFRRTVYSSNVSPACYEDMGNNTANWRMLLRILPQSFGFIVPLLIMLFCYGFTLRTLFK
AHMGQKHRAMRVIFAVVLIFLLCWLPYNLVLLADTLMRTQVIQETCERRNHIDRALDATE
ILGILHSCLNPLIYAFIGQKFRHGLLKILAIHGLISKDSLPKDSRPSFVGSSSGHTSTTL
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BDBM50113636 |
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n/a |
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Name | BDBM50113636 |
Synonyms: | CHEMBL39835 | [5-(4-Fluoro-phenylcarbamoyl)-pyridin-2-ylsulfanyl]-acetic acid |
Type | Small organic molecule |
Emp. Form. | C14H11FN2O3S |
Mol. Mass. | 306.312 |
SMILES | OC(=O)CSc1ccc(cn1)C(=O)Nc1ccc(F)cc1 |
Structure |
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