Reaction Details |
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Target | C-X-C chemokine receptor type 3 |
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Ligand | BDBM50412596 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_560732 (CHEMBL1010867) |
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IC50 | 794.33±n/a nM |
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Citation | Wang, Y; Busch-Petersen, J; Wang, F; Kiesow, TJ; Graybill, TL; Jin, J; Yang, Z; Foley, JJ; Hunsberger, GE; Schmidt, DB; Sarau, HM; Capper-Spudich, EA; Wu, Z; Fisher, LS; McQueney, MS; Rivero, RA; Widdowson, KL Camphor sulfonamide derivatives as novel, potent and selective CXCR3 antagonists. Bioorg Med Chem Lett19:114-8 (2008) [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 3 |
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Name: | C-X-C chemokine receptor type 3 |
Synonyms: | AAO92295.1 | C-X-C chemokine receptor type 3 | C-X-C chemokine receptor type 3 (CXCR3) | C-X-C chemokine receptor type 3 (CXCR3A) | CXCR3 | CXCR3A | CXCR3_HUMAN | GPR9 | chemokine (C-X-C motif) receptor 3 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 40665.65 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 368 |
Sequence: | MVLEVSDHQVLNDAEVAALLENFSSSYDYGENESDSCCTSPPCPQDFSLNFDRAFLPALY
SLLFLLGLLGNGAVAAVLLSRRTALSSTDTFLLHLAVADTLLVLTLPLWAVDAAVQWVFG
SGLCKVAGALFNINFYAGALLLACISFDRYLNIVHATQLYRRGPPARVTLTCLAVWGLCL
LFALPDFIFLSAHHDERLNATHCQYNFPQVGRTALRVLQLVAGFLLPLLVMAYCYAHILA
VLLVSRGQRRLRAMRLVVVVVVAFALCWTPYHLVVLVDILMDLGALARNCGRESRVDVAK
SVTSGLGYMHCCLNPLLYAFVGVKFRERMWMLLLRLGCPNQRGLQRQPSSSRRDSSWSET
SEASYSGL
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BDBM50412596 |
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n/a |
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Name | BDBM50412596 |
Synonyms: | CHEMBL517402 |
Type | Small organic molecule |
Emp. Form. | C20H27F4N3O2S |
Mol. Mass. | 449.506 |
SMILES | CC1(C)[C@@H]2CC[C@@]1(CS(=O)(=O)N1CCN(CC1)c1ccc(cn1)C(F)(F)F)C(F)C2 |r,THB:28:27:5.4:1| |
Structure |
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