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TargetC-C chemokine receptor type 5
LigandBDBM50148680
Substrate/Competitorn/a
Meas. Tech.ChEBML_39655
IC50 15000±n/a nM
Citation Shankaran, KDonnelly, KLShah, SKCaldwell, CGChen, PFinke, PEOates, BMacCoss, MMills, SGDeMartino, JAGould, SLMalkowitz, LSiciliano, SJSpringer, MSKwei, GCarella, ACarver, GDanzeisen, RHazuda, DHolmes, KKessler, JLineberger, JMiller, MDEmini, EASchleif, WA Syntheses and biological evaluation of 5-(piperidin-1-yl)-3-phenyl-pentylsulfones as CCR5 antagonists. Bioorg Med Chem Lett14:3589-93 (2004) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
C-C chemokine receptor type 5
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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  Blast E-value cutoff:
BDBM50148680
n/a
NameBDBM50148680
Synonyms:Allyl-[1-(6-oxo-3,6-diphenyl-hexyl)-piperidin-4-yl]-carbamic acid 4-nitro-benzyl ester | CHEMBL118501
TypeSmall organic molecule
Emp. Form.C34H39N3O5
Mol. Mass.569.6906
SMILES[O-][N+](=O)c1ccc(COC(=O)N(CC=C)C2CCN(CCC(CCC(=O)c3ccccc3)c3ccccc3)CC2)cc1
Structure
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