Reaction Details |
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Target | C-C chemokine receptor type 5 |
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Ligand | BDBM50267125 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1702178 (CHEMBL4053411) |
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Kd | 10.0±n/a nM |
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Citation | Schwehm, C; Kellam, B; Garces, AE; Hill, SJ; Kindon, ND; Bradshaw, TD; Li, J; Macdonald, SJ; Rowedder, JE; Stoddart, LA; Stocks, MJ Design and Elaboration of a Tractable Tricyclic Scaffold To Synthesize Druglike Inhibitors of Dipeptidyl Peptidase-4 (DPP-4), Antagonists of the C-C Chemokine Receptor Type 5 (CCR5), and Highly Potent and Selective Phosphoinositol-3 Kinase? (PI3K?) Inhibitors. J Med Chem60:1534-1554 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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C-C chemokine receptor type 5 |
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Name: | C-C chemokine receptor type 5 |
Synonyms: | C-C CKR-5 | C-C chemokine receptor type 5 | CC-CKR-5 | CCR-5 | CCR5 | CCR5/mu opioid receptor complex | CCR5_HUMAN | CD_antigen=CD195 | CHEMR13 | CMKBR5 | HIV-1 fusion coreceptor |
Type: | Enzyme |
Mol. Mass.: | 40540.21 |
Organism: | Homo sapiens (Human) |
Description: | P51681 |
Residue: | 352 |
Sequence: | MDYQVSSPIYDINYYTSEPCQKINVKQIAARLLPPLYSLVFIFGFVGNMLVILILINCKR
LKSMTDIYLLNLAISDLFFLLTVPFWAHYAAAQWDFGNTMCQLLTGLYFIGFFSGIFFII
LLTIDRYLAVVHAVFALKARTVTFGVVTSVITWVVAVFASLPGIIFTRSQKEGLHYTCSS
HFPYSQYQFWKNFQTLKIVILGLVLPLLVMVICYSGILKTLLRCRNEKKRHRAVRLIFTI
MIVYFLFWAPYNIVLLLNTFQEFFGLNNCSSSNRLDQAMQVTETLGMTHCCINPIIYAFV
GEKFRNYLLVFFQKHIAKRFCKCCSIFQQEAPERASSVYTRSTGEQEISVGL
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BDBM50267125 |
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n/a |
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Name | BDBM50267125 |
Synonyms: | CHEMBL4089991 |
Type | Small organic molecule |
Emp. Form. | C26H35F2N5O |
Mol. Mass. | 471.5858 |
SMILES | [H][C@@]12CCc3nnc(C)n3[C@]1([H])CCN(CC[C@H](NC(=O)C1CCC(F)(F)CC1)c1ccccc1)C2 |r| |
Structure |
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