Reaction Details |
| Report a problem with these data |
Target | C-C chemokine receptor type 4 |
---|
Ligand | BDBM50142382 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEBML_39491 |
---|
IC50 | 9000±n/a nM |
---|
Citation | Allen, S; Newhouse, B; Anderson, AS; Fauber, B; Allen, A; Chantry, D; Eberhardt, C; Odingo, J; Burgess, LE Discovery and SAR of trisubstituted thiazolidinones as CCR4 antagonists. Bioorg Med Chem Lett14:1619-24 (2004) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
C-C chemokine receptor type 4 |
---|
Name: | C-C chemokine receptor type 4 |
Synonyms: | C-C CKR-4 | C-C chemokine receptor type 4 | C-C chemokine receptor type 4 (CCR4) | CC-CKR-4 | CCR-4 | CCR4 | CCR4_HUMAN | CD_antigen=CD194 | CMKBR4 | K5-5 |
Type: | Enzyme |
Mol. Mass.: | 41406.41 |
Organism: | Homo sapiens (Human) |
Description: | P51679 |
Residue: | 360 |
Sequence: | MNPTDIADTTLDESIYSNYYLYESIPKPCTKEGIKAFGELFLPPLYSLVFVFGLLGNSVV
VLVLFKYKRLRSMTDVYLLNLAISDLLFVFSLPFWGYYAADQWVFGLGLCKMISWMYLVG
FYSGIFFVMLMSIDRYLAIVHAVFSLRARTLTYGVITSLATWSVAVFASLPGFLFSTCYT
ERNHTYCKTKYSLNSTTWKVLSSLEINILGLVIPLGIMLFCYSMIIRTLQHCKNEKKNKA
VKMIFAVVVLFLGFWTPYNIVLFLETLVELEVLQDCTFERYLDYAIQATETLAFVHCCLN
PIIYFFLGEKFRKYILQLFKTCRGLFVLCQYCGLLQIYSADTPSSSYTQSTMDHDLHDAL
|
|
|
BDBM50142382 |
---|
n/a |
---|
Name | BDBM50142382 |
Synonyms: | 2-[(2R,5R)-2-(2,4-Dichloro-phenyl)-3-(2-morpholin-4-yl-ethyl)-4-oxo-thiazolidin-5-yl]-N-naphthalen-1-ylmethyl-acetamide | CHEMBL295405 |
Type | Small organic molecule |
Emp. Form. | C28H29Cl2N3O3S |
Mol. Mass. | 558.519 |
SMILES | Clc1ccc([C@H]2S[C@H](CC(=O)NCc3cccc4ccccc34)C(=O)N2CCN2CCOCC2)c(Cl)c1 |
Structure |
|