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SMILES: Cc1cccc(C)c1-c1ccc(C[N+](C)(C)CC2=CC[C@H]3C[C@@H]2C3(C)C)cc1

InChI Key: InChIKey=OSBODHIZQIUNQR-DQEYMECFSA-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 2 hits for monomerid = 50400004   
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-X-C chemokine receptor type 3


(Homo sapiens (Human))
BDBM50400004
PNG
(CHEMBL2181465)
Show SMILES Cc1cccc(C)c1-c1ccc(C[N+](C)(C)CC2=CC[C@H]3C[C@@H]2C3(C)C)cc1 |r,t:18|
Show InChI InChI=1S/C27H36N/c1-19-8-7-9-20(2)26(19)22-12-10-21(11-13-22)17-28(5,6)18-23-14-15-24-16-25(23)27(24,3)4/h7-14,24-25H,15-18H2,1-6H3/q+1/t24-,25-/m0/s1
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
1.00E+3n/an/an/an/an/an/an/an/a



VU University Amsterdam

Curated by ChEMBL


Assay Description
Displacement of [125I]CXCL10 from CXCR3 expressed in HEK293 cells


J Med Chem 55: 10572-83 (2012)


Article DOI: 10.1021/jm301240t
BindingDB Entry DOI: 10.7270/Q27P90J8
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 3


(Homo sapiens (Human))
BDBM50400004
PNG
(CHEMBL2181465)
Show SMILES Cc1cccc(C)c1-c1ccc(C[N+](C)(C)CC2=CC[C@H]3C[C@@H]2C3(C)C)cc1 |r,t:18|
Show InChI InChI=1S/C27H36N/c1-19-8-7-9-20(2)26(19)22-12-10-21(11-13-22)17-28(5,6)18-23-14-15-24-16-25(23)27(24,3)4/h7-14,24-25H,15-18H2,1-6H3/q+1/t24-,25-/m0/s1
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 7.94E+3n/an/an/an/a



VU University Amsterdam

Curated by ChEMBL


Assay Description
Agonist activity at CXCR3 expressed in HEK293 cells by [35S]GTPgamma binding assay


J Med Chem 55: 10572-83 (2012)


Article DOI: 10.1021/jm301240t
BindingDB Entry DOI: 10.7270/Q27P90J8
More data for this
Ligand-Target Pair