Reaction Details |
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Target | C-C chemokine receptor type 1 |
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Ligand | BDBM50422828 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_338815 (CHEMBL860547) |
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IC50 | >10000±n/a nM |
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Citation | Seto, M; Aikawa, K; Miyamoto, N; Aramaki, Y; Kanzaki, N; Takashima, K; Kuze, Y; Iizawa, Y; Baba, M; Shiraishi, M Highly potent and orally active CCR5 antagonists as anti-HIV-1 agents: synthesis and biological activities of 1-benzazocine derivatives containing a sulfoxide moiety. J Med Chem49:2037-48 (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 1 |
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Name: | C-C chemokine receptor type 1 |
Synonyms: | C-C CKR-1 | C-C chemokine receptor type 1 (CCR1) | CC-CKR-1 | CCR-1 | CCR1 | CCR1_HUMAN | CD_antigen=CD191 | CMKBR1 | CMKR1 | HM145 | LD78 receptor | MIP-1alpha-R | Macrophage inflammatory protein 1-alpha receptor | RANTES-R | SCYAR1 |
Type: | Enzyme |
Mol. Mass.: | 41180.69 |
Organism: | Homo sapiens (Human) |
Description: | P32246 |
Residue: | 355 |
Sequence: | METPNTTEDYDTTTEFDYGDATPCQKVNERAFGAQLLPPLYSLVFVIGLVGNILVVLVLV
QYKRLKNMTSIYLLNLAISDLLFLFTLPFWIDYKLKDDWVFGDAMCKILSGFYYTGLYSE
IFFIILLTIDRYLAIVHAVFALRARTVTFGVITSIIIWALAILASMPGLYFSKTQWEFTH
HTCSLHFPHESLREWKLFQALKLNLFGLVLPLLVMIICYTGIIKILLRRPNEKKSKAVRL
IFVIMIIFFLFWTPYNLTILISVFQDFLFTHECEQSRHLDLAVQVTEVIAYTHCCVNPVI
YAFVGERFRKYLRQLFHRRVAVHLVKWLPFLSVDRLERVSSTSPSTGEHELSAGF
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BDBM50422828 |
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n/a |
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Name | BDBM50422828 |
Synonyms: | CENICRIVIROC | CENICRIVIROC MESYLATE | TAK-652 | TBR-652 |
Type | Small organic molecule |
Emp. Form. | C41H52N4O4S |
Mol. Mass. | 696.941 |
SMILES | CCCCOCCOc1ccc(cc1)-c1ccc2N(CC(C)C)CCCC(=Cc2c1)C(=O)Nc1ccc(cc1)[S@@](=O)Cc1cncn1CCC |r,w:27.28| |
Structure |
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