Reaction Details |
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Target | C-X-C chemokine receptor type 1 |
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Ligand | BDBM50150559 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_306397 (CHEMBL828738) |
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IC50 | 3100±n/a nM |
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Citation | Weidner-Wells, MA; Henninger, TC; Fraga-Spano, SA; Boggs, CM; Matheis, M; Ritchie, DM; Argentieri, DC; Wachter, MP; Hlasta, DJ Synthesis and structure-activity relationships of 3,5-diarylisoxazoles and 3,5-diaryl-1,2,4-oxadiazoles, novel classes of small molecule interleukin-8 (IL-8) receptor antagonists. Bioorg Med Chem Lett14:4307-11 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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C-X-C chemokine receptor type 1 |
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Name: | C-X-C chemokine receptor type 1 |
Synonyms: | C-X-C chemokine receptor type 1 (CXCR-1) | C-X-C chemokine receptor type 1 (CXCR1) | CMKAR1 | CXCR1 | CXCR1_HUMAN | IL8RA | Interleukin-8 receptor A | Interleukin-8 receptors, CXCR1/CXCR2 |
Type: | Enzyme |
Mol. Mass.: | 39803.83 |
Organism: | Homo sapiens (Human) |
Description: | P25024 |
Residue: | 350 |
Sequence: | MSNITDPQMWDFDDLNFTGMPPADEDYSPCMLETETLNKYVVIIAYALVFLLSLLGNSLV
MLVILYSRVGRSVTDVYLLNLALADLLFALTLPIWAASKVNGWIFGTFLCKVVSLLKEVN
FYSGILLLACISVDRYLAIVHATRTLTQKRHLVKFVCLGCWGLSMNLSLPFFLFRQAYHP
NNSSPVCYEVLGNDTAKWRMVLRILPHTFGFIVPLFVMLFCYGFTLRTLFKAHMGQKHRA
MRVIFAVVLIFLLCWLPYNLVLLADTLMRTQVIQESCERRNNIGRALDATEILGFLHSCL
NPIIYAFIGQNFRHGFLKILAMHGLVSKEFLARHRVTSYTSSSVNVSSNL
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BDBM50150559 |
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n/a |
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Name | BDBM50150559 |
Synonyms: | CHEMBL182361 | {4-[5-(4-Fluoro-phenyl)-isoxazol-3-yl]-phenoxymethyl}-dimethyl-amine |
Type | Small organic molecule |
Emp. Form. | C18H17FN2O2 |
Mol. Mass. | 312.3382 |
SMILES | CN(C)COc1ccc(cc1)-c1cc(on1)-c1ccc(F)cc1 |
Structure |
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