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BDBM50420012 CHEMBL2032303

SMILES: CC(C)Oc1ccc(cc1Cl)-c1nc2cc(cnc2o1)C(O)=O

InChI Key: InChIKey=GIPLGGPOGWHPSQ-UHFFFAOYSA-N

Data: 2 EC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50420012   
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
Sphingosine 1-phosphate receptor 1


(Homo sapiens (Human))
BDBM50420012
PNG
(CHEMBL2032303)
Show SMILES CC(C)Oc1ccc(cc1Cl)-c1nc2cc(cnc2o1)C(O)=O
Show InChI InChI=1S/C16H13ClN2O4/c1-8(2)22-13-4-3-9(5-11(13)17)14-19-12-6-10(16(20)21)7-18-15(12)23-14/h3-8H,1-2H3,(H,20,21)
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antibodypedia
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PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a>3.16E+3n/an/an/an/a



GlaxoSmithKline Pharmaceuticals

Curated by ChEMBL


Assay Description
Agonist activity at SIP1 receptor by tango assay


Bioorg Med Chem Lett 22: 3973-7 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.095
BindingDB Entry DOI: 10.7270/Q29P32NS
More data for this
Ligand-Target Pair
Sphingosine 1-phosphate receptor 3


(Homo sapiens (Human))
BDBM50420012
PNG
(CHEMBL2032303)
Show SMILES CC(C)Oc1ccc(cc1Cl)-c1nc2cc(cnc2o1)C(O)=O
Show InChI InChI=1S/C16H13ClN2O4/c1-8(2)22-13-4-3-9(5-11(13)17)14-19-12-6-10(16(20)21)7-18-15(12)23-14/h3-8H,1-2H3,(H,20,21)
PDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a>1.00E+4n/an/an/an/a



GlaxoSmithKline Pharmaceuticals

Curated by ChEMBL


Assay Description
Agonist activity at human SIP3 receptor assessed as calcium mobilization by GeneBLAzer assay


Bioorg Med Chem Lett 22: 3973-7 (2012)


Article DOI: 10.1016/j.bmcl.2012.04.095
BindingDB Entry DOI: 10.7270/Q29P32NS
More data for this
Ligand-Target Pair