BindingDB logo
myBDB logout

null

SMILES: O[C@]1(CC[C@@H](CC1)N1CC[C@H](C1)NC(=O)CNC(=O)c1cccc(c1)C(F)(F)F)c1cnccn1

InChI Key: InChIKey=VVCJMAZMIRREGR-DNVFCKCGSA-N

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 3 hits for monomerid = 50363951   
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))
BDBM50363951
PNG
(CHEMBL1951776)
Show SMILES O[C@]1(CC[C@@H](CC1)N1CC[C@H](C1)NC(=O)CNC(=O)c1cccc(c1)C(F)(F)F)c1cnccn1 |r,wU:4.7,wD:10.13,1.0,(-5.05,-16.35,;-4.27,-17.69,;-3.46,-19.01,;-1.93,-18.98,;-1.18,-17.63,;-1.98,-16.31,;-3.53,-16.34,;.36,-17.6,;1.28,-18.82,;2.73,-18.32,;2.7,-16.78,;1.23,-16.33,;4.03,-15.99,;5.37,-16.75,;5.39,-18.29,;6.7,-15.96,;8.04,-16.71,;9.36,-15.93,;9.34,-14.39,;10.71,-16.68,;10.72,-18.22,;12.06,-18.97,;13.38,-18.18,;13.36,-16.64,;12.02,-15.89,;14.68,-15.85,;16.03,-16.59,;14.66,-14.31,;16.01,-15.07,;-5.81,-17.73,;-6.61,-16.41,;-8.15,-16.45,;-8.89,-17.8,;-8.1,-19.12,;-6.55,-19.09,)|
Show InChI InChI=1S/C24H28F3N5O3/c25-24(26,27)17-3-1-2-16(12-17)22(34)30-14-21(33)31-18-6-11-32(15-18)19-4-7-23(35,8-5-19)20-13-28-9-10-29-20/h1-3,9-10,12-13,18-19,35H,4-8,11,14-15H2,(H,30,34)(H,31,33)/t18-,19-,23-/m1/s1
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 10.9n/an/an/an/an/an/a



TBA

Curated by ChEMBL


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


ACS Med Chem Lett 2: 450-454 (2011)


Article DOI: 10.1021/ml200030q
BindingDB Entry DOI: 10.7270/Q2WD4116
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50363951
PNG
(CHEMBL1951776)
Show SMILES O[C@]1(CC[C@@H](CC1)N1CC[C@H](C1)NC(=O)CNC(=O)c1cccc(c1)C(F)(F)F)c1cnccn1 |r,wU:4.7,wD:10.13,1.0,(-5.05,-16.35,;-4.27,-17.69,;-3.46,-19.01,;-1.93,-18.98,;-1.18,-17.63,;-1.98,-16.31,;-3.53,-16.34,;.36,-17.6,;1.28,-18.82,;2.73,-18.32,;2.7,-16.78,;1.23,-16.33,;4.03,-15.99,;5.37,-16.75,;5.39,-18.29,;6.7,-15.96,;8.04,-16.71,;9.36,-15.93,;9.34,-14.39,;10.71,-16.68,;10.72,-18.22,;12.06,-18.97,;13.38,-18.18,;13.36,-16.64,;12.02,-15.89,;14.68,-15.85,;16.03,-16.59,;14.66,-14.31,;16.01,-15.07,;-5.81,-17.73,;-6.61,-16.41,;-8.15,-16.45,;-8.89,-17.8,;-8.1,-19.12,;-6.55,-19.09,)|
Show InChI InChI=1S/C24H28F3N5O3/c25-24(26,27)17-3-1-2-16(12-17)22(34)30-14-21(33)31-18-6-11-32(15-18)19-4-7-23(35,8-5-19)20-13-28-9-10-29-20/h1-3,9-10,12-13,18-19,35H,4-8,11,14-15H2,(H,30,34)(H,31,33)/t18-,19-,23-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>30n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Displacement of dofetidine from human Erg


ACS Med Chem Lett 2: 450-454 (2011)


Article DOI: 10.1021/ml200030q
BindingDB Entry DOI: 10.7270/Q2WD4116
More data for this
Ligand-Target Pair
C-C chemokine receptor type 2


(Homo sapiens (Human))
BDBM50363951
PNG
(CHEMBL1951776)
Show SMILES O[C@]1(CC[C@@H](CC1)N1CC[C@H](C1)NC(=O)CNC(=O)c1cccc(c1)C(F)(F)F)c1cnccn1 |r,wU:4.7,wD:10.13,1.0,(-5.05,-16.35,;-4.27,-17.69,;-3.46,-19.01,;-1.93,-18.98,;-1.18,-17.63,;-1.98,-16.31,;-3.53,-16.34,;.36,-17.6,;1.28,-18.82,;2.73,-18.32,;2.7,-16.78,;1.23,-16.33,;4.03,-15.99,;5.37,-16.75,;5.39,-18.29,;6.7,-15.96,;8.04,-16.71,;9.36,-15.93,;9.34,-14.39,;10.71,-16.68,;10.72,-18.22,;12.06,-18.97,;13.38,-18.18,;13.36,-16.64,;12.02,-15.89,;14.68,-15.85,;16.03,-16.59,;14.66,-14.31,;16.01,-15.07,;-5.81,-17.73,;-6.61,-16.41,;-8.15,-16.45,;-8.89,-17.8,;-8.1,-19.12,;-6.55,-19.09,)|
Show InChI InChI=1S/C24H28F3N5O3/c25-24(26,27)17-3-1-2-16(12-17)22(34)30-14-21(33)31-18-6-11-32(15-18)19-4-7-23(35,8-5-19)20-13-28-9-10-29-20/h1-3,9-10,12-13,18-19,35H,4-8,11,14-15H2,(H,30,34)(H,31,33)/t18-,19-,23-/m1/s1
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 10.4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Antagonist activity at CCR2 in human PBMC assessed as inhibition of MCP1-induced chemotaxis after 30 mins


ACS Med Chem Lett 2: 450-454 (2011)


Article DOI: 10.1021/ml200030q
BindingDB Entry DOI: 10.7270/Q2WD4116
More data for this
Ligand-Target Pair