Reaction Details |
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Target | C-C chemokine receptor type 5 |
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Ligand | BDBM50197778 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_453280 (CHEMBL902435) |
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IC50 | 1400±n/a nM |
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Citation | Wei, RG; Arnaiz, DO; Chou, YL; Davey, D; Dunning, L; Lee, W; Lu, SF; Onuffer, J; Ye, B; Phillips, G CCR5 receptor antagonists: discovery and SAR study of guanylhydrazone derivatives. Bioorg Med Chem Lett17:231-4 (2006) [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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BDBM50197778 |
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n/a |
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Name | BDBM50197778 |
Synonyms: | CHEMBL234634 | N-(2-(4-chlorobenzyloxy)-5-bromobenzyl)-N-ethylethanamine |
Type | Small organic molecule |
Emp. Form. | C18H21BrClNO |
Mol. Mass. | 382.722 |
SMILES | CCN(CC)Cc1cc(Br)ccc1OCc1ccc(Cl)cc1 |
Structure |
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