BDBM50335449 1-(4-(5-cyclohexylbenzofuran-2-yl)benzyl)azetidine-3-carboxylic acid::CHEMBL1651703

SMILES: OC(=O)C1CN(Cc2ccc(cc2)-c2cc3cc(ccc3o2)C2CCCCC2)C1

InChI Key: InChIKey=HGHYQVXLKNDCDC-UHFFFAOYSA-N

Data: 3 EC50

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 = 50335449   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Sphingosine 1-phosphate receptor 1 (Homo sapiens (Human))	BDBM50335449 (1-(4-(5-cyclohexylbenzofuran-2-yl)benzyl)azetidine...) Show SMILES OC(=O)C1CN(Cc2ccc(cc2)-c2cc3cc(ccc3o2)C2CCCCC2)C1 Show InChI InChI=1S/C25H27NO3/c27-25(28)22-15-26(16-22)14-17-6-8-19(9-7-17)24-13-21-12-20(10-11-23(21)29-24)18-4-2-1-3-5-18/h6-13,18,22H,1-5,14-16H2,(H,27,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	600	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Agonist activity at human S1P1R expressed in CHO cells assessed as stimulation of [35S]GTPgammaS binding				ACS Med Chem Lett 2: 97-101 (2011) Article DOI: 10.1021/ml100227q BindingDB Entry DOI: 10.7270/Q2WM1DP6
					More data for this Ligand-Target Pair
Sphingosine 1-phosphate receptor 1 (Homo sapiens (Human))	BDBM50335449 (1-(4-(5-cyclohexylbenzofuran-2-yl)benzyl)azetidine...) Show SMILES OC(=O)C1CN(Cc2ccc(cc2)-c2cc3cc(ccc3o2)C2CCCCC2)C1 Show InChI InChI=1S/C25H27NO3/c27-25(28)22-15-26(16-22)14-17-6-8-19(9-7-17)24-13-21-12-20(10-11-23(21)29-24)18-4-2-1-3-5-18/h6-13,18,22H,1-5,14-16H2,(H,27,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	460	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Induction of human GFP-tagged chimeric S1P1R internalization in human U2Os cells by fluorescence microscopy				ACS Med Chem Lett 2: 97-101 (2011) Article DOI: 10.1021/ml100227q BindingDB Entry DOI: 10.7270/Q2WM1DP6
					More data for this Ligand-Target Pair
Sphingosine 1-phosphate receptor 3 (Homo sapiens (Human))	BDBM50335449 (1-(4-(5-cyclohexylbenzofuran-2-yl)benzyl)azetidine...) Show SMILES OC(=O)C1CN(Cc2ccc(cc2)-c2cc3cc(ccc3o2)C2CCCCC2)C1 Show InChI InChI=1S/C25H27NO3/c27-25(28)22-15-26(16-22)14-17-6-8-19(9-7-17)24-13-21-12-20(10-11-23(21)29-24)18-4-2-1-3-5-18/h6-13,18,22H,1-5,14-16H2,(H,27,28)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	>2.50E+4	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Agonist activity at human S1P3R expressed in CHO cells by Ca(2+) mobilization assay				ACS Med Chem Lett 2: 97-101 (2011) Article DOI: 10.1021/ml100227q BindingDB Entry DOI: 10.7270/Q2WM1DP6
					More data for this Ligand-Target Pair