Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetC-C motif chemokine 5
LigandBDBM50329241
Substrate/Competitorn/a
Meas. Tech.ChEMBL_675123 (CHEMBL1272914)
IC50 23±n/a nM
Citation Wanner, JChen, LLemoine, RCKondru, RJekle, AHeilek, GdeRosier, AJi, CBerry, PWRotstein, DM Evaluation of amide replacements in CCR5 antagonists as a means to increase intrinsic permeability. Part 2: SAR optimization and pharmacokinetic profile of a homologous azacyle series. Bioorg Med Chem Lett20:6802-7 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
C-C motif chemokine 5
Name:C-C motif chemokine 5
Synonyms:CCL5 | CCL5_HUMAN | D17S136E | EoCP | Eosinophil chemotactic cytokine | RANTES(3-68) | RANTES(4-68) | SCYA5 | SIS-delta | Small-inducible cytokine A5 | T cell-specific protein P228 | T-cell-specific protein RANTES | TCP228
Type:PROTEIN
Mol. Mass.:9996.11
Organism:Homo sapiens (Human)
Description:ChEMBL_1363187
Residue:91
Sequence:
MKVSAAALAVILIATALCAPASASPYSSDTTPCCFAYIARPLPRAHIKEYFYTSGKCSNP
AVVFVTRKNRQVCANPEKKWVREYINSLEMS
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50329241
n/a
NameBDBM50329241
Synonyms:(4,6-dimethylpyrimidin-5-yl)((3aR,6aS)-5-(3-(1-(isopropylsulfonyl)azetidin-3-yl)-3-phenylpropyl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)methanone | CHEMBL1270101
TypeSmall organic molecule
Emp. Form.C28H39N5O3S
Mol. Mass.525.706
SMILESCC(C)S(=O)(=O)N1CC(C1)C(CCN1C[C@H]2CN(C[C@H]2C1)C(=O)c1c(C)ncnc1C)c1ccccc1 |r|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: