BindingDB logo
myBDB logout

BDBM50009211 CHEMBL3233178

SMILES: CC(C)N(C)[C@@H]1CC[C@@H]([C@H](CS(C)(=O)=O)C1)N1CC[C@H](NC(=O)c2cccc(c2)C(F)(F)F)C1=O

InChI Key: InChIKey=KZYUPKXEHNEFIY-NRDMVMEKSA-N

Data: 5 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50009211   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
C-C chemokine receptor type 2


(Homo sapiens (Human))
BDBM50009211
PNG
(CHEMBL3233178)
Show SMILES CC(C)N(C)[C@@H]1CC[C@@H]([C@H](CS(C)(=O)=O)C1)N1CC[C@H](NC(=O)c2cccc(c2)C(F)(F)F)C1=O |r|
Show InChI InChI=1S/C24H34F3N3O4S/c1-15(2)29(3)19-8-9-21(17(13-19)14-35(4,33)34)30-11-10-20(23(30)32)28-22(31)16-6-5-7-18(12-16)24(25,26)27/h5-7,12,15,17,19-21H,8-11,13-14H2,1-4H3,(H,28,31)/t17-,19+,20-,21-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.80n/an/an/an/an/an/a



Bristol-Myers Squibb Company

Curated by ChEMBL


Assay Description
Displacement of [125I]-labeled human MCP1 from CCR2 in human PBMC


Bioorg Med Chem Lett 24: 1843-5 (2014)


Article DOI: 10.1016/j.bmcl.2014.02.013
BindingDB Entry DOI: 10.7270/Q2FQ9Z4P
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50009211
PNG
(CHEMBL3233178)
Show SMILES CC(C)N(C)[C@@H]1CC[C@@H]([C@H](CS(C)(=O)=O)C1)N1CC[C@H](NC(=O)c2cccc(c2)C(F)(F)F)C1=O |r|
Show InChI InChI=1S/C24H34F3N3O4S/c1-15(2)29(3)19-8-9-21(17(13-19)14-35(4,33)34)30-11-10-20(23(30)32)28-22(31)16-6-5-7-18(12-16)24(25,26)27/h5-7,12,15,17,19-21H,8-11,13-14H2,1-4H3,(H,28,31)/t17-,19+,20-,21-/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>8.00E+4n/an/an/an/an/an/a



Bristol-Myers Squibb Company

Curated by ChEMBL


Assay Description
Inhibition of human ERG by FLIPR assay


Bioorg Med Chem Lett 24: 1843-5 (2014)


Article DOI: 10.1016/j.bmcl.2014.02.013
BindingDB Entry DOI: 10.7270/Q2FQ9Z4P
More data for this
Ligand-Target Pair
CCR5/mu opioid receptor complex


(Homo sapiens (Human))
BDBM50009211
PNG
(CHEMBL3233178)
Show SMILES CC(C)N(C)[C@@H]1CC[C@@H]([C@H](CS(C)(=O)=O)C1)N1CC[C@H](NC(=O)c2cccc(c2)C(F)(F)F)C1=O |r|
Show InChI InChI=1S/C24H34F3N3O4S/c1-15(2)29(3)19-8-9-21(17(13-19)14-35(4,33)34)30-11-10-20(23(30)32)28-22(31)16-6-5-7-18(12-16)24(25,26)27/h5-7,12,15,17,19-21H,8-11,13-14H2,1-4H3,(H,28,31)/t17-,19+,20-,21-/m0/s1
PDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.64E+3n/an/an/an/an/an/a



Bristol-Myers Squibb Company

Curated by ChEMBL


Assay Description
Antagonist activity at CCR5 (unknown origin) expressed in human HT1080 cells assessed as blockade of MIP1beta-binding to receptor


ACS Med Chem Lett 10: 300-305 (2019)


Article DOI: 10.1021/acsmedchemlett.8b00439
More data for this
Ligand-Target Pair
C-C chemokine receptor type 2


(Homo sapiens (Human))
BDBM50009211
PNG
(CHEMBL3233178)
Show SMILES CC(C)N(C)[C@@H]1CC[C@@H]([C@H](CS(C)(=O)=O)C1)N1CC[C@H](NC(=O)c2cccc(c2)C(F)(F)F)C1=O |r|
Show InChI InChI=1S/C24H34F3N3O4S/c1-15(2)29(3)19-8-9-21(17(13-19)14-35(4,33)34)30-11-10-20(23(30)32)28-22(31)16-6-5-7-18(12-16)24(25,26)27/h5-7,12,15,17,19-21H,8-11,13-14H2,1-4H3,(H,28,31)/t17-,19+,20-,21-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.80n/an/an/an/an/an/a



Bristol-Myers Squibb Company

Curated by ChEMBL


Assay Description
Displacement of [125I]MCP1 from CCR2 in human PBMC measured after 30 mins


ACS Med Chem Lett 10: 300-305 (2019)


Article DOI: 10.1021/acsmedchemlett.8b00439
More data for this
Ligand-Target Pair
C-C chemokine receptor type 2


(Homo sapiens (Human))
BDBM50009211
PNG
(CHEMBL3233178)
Show SMILES CC(C)N(C)[C@@H]1CC[C@@H]([C@H](CS(C)(=O)=O)C1)N1CC[C@H](NC(=O)c2cccc(c2)C(F)(F)F)C1=O |r|
Show InChI InChI=1S/C24H34F3N3O4S/c1-15(2)29(3)19-8-9-21(17(13-19)14-35(4,33)34)30-11-10-20(23(30)32)28-22(31)16-6-5-7-18(12-16)24(25,26)27/h5-7,12,15,17,19-21H,8-11,13-14H2,1-4H3,(H,28,31)/t17-,19+,20-,21-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 2.60n/an/an/an/an/an/a



Bristol-Myers Squibb Company

Curated by ChEMBL


Assay Description
Antagonist activity at CCR2 in human monocytes assessed as reduction of chemotaxis in presence of 0.1 M BSA


Bioorg Med Chem Lett 24: 1843-5 (2014)


Article DOI: 10.1016/j.bmcl.2014.02.013
BindingDB Entry DOI: 10.7270/Q2FQ9Z4P
More data for this
Ligand-Target Pair