BDBM50128714 (+) 7-[3-(4-Methoxy-benzenesulfonylamino)-bicyclo[2.2.1]hept-2-yl]-hept-5-enoic acid::CHEMBL79522

SMILES: COc1ccc(cc1)S(=O)(=O)N[C@@H]1[C@@H]2CC[C@@H](C2)[C@H]1C\C=C/CCCC(O)=O

InChI Key: InChIKey=VCOYWENAIWGYDI-ZKMBTSHHSA-N

Data: 2 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 2 hits for monomerid = 50128714   

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
Prostanoid DP receptor (Homo sapiens (Human))	BDBM50128714 ((+) 7-[3-(4-Methoxy-benzenesulfonylamino)-bicyclo[...) Show SMILES COc1ccc(cc1)S(=O)(=O)N[C@@H]1[C@@H]2CC[C@@H](C2)[C@H]1C\C=C/CCCC(O)=O Show InChI InChI=1S/C21H29NO5S/c1-27-17-10-12-18(13-11-17)28(25,26)22-21-16-9-8-15(14-16)19(21)6-4-2-3-5-7-20(23)24/h2,4,10-13,15-16,19,21-22H,3,5-9,14H2,1H3,(H,23,24)/b4-2-/t15-,16+,19+,21+/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description In vitro inhibition of [3H]- PGD-2 radioligand binding to prostaglandin D2 receptor on human platelet membrane				J Med Chem 46: 2436-45 (2003) Article DOI: 10.1021/jm020517g BindingDB Entry DOI: 10.7270/Q2154GFS
					More data for this Ligand-Target Pair
Prostanoid DP receptor (Homo sapiens (Human))	BDBM50128714 ((+) 7-[3-(4-Methoxy-benzenesulfonylamino)-bicyclo[...) Show SMILES COc1ccc(cc1)S(=O)(=O)N[C@@H]1[C@@H]2CC[C@@H](C2)[C@H]1C\C=C/CCCC(O)=O Show InChI InChI=1S/C21H29NO5S/c1-27-17-10-12-18(13-11-17)28(25,26)22-21-16-9-8-15(14-16)19(21)6-4-2-3-5-7-20(23)24/h2,4,10-13,15-16,19,21-22H,3,5-9,14H2,1H3,(H,23,24)/b4-2-/t15-,16+,19+,21+/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	390	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi & Co., Ltd. Curated by ChEMBL					Assay Description In vitro inhibition of cAMP formation evoked by prostaglandin D2 receptor in human platelets				J Med Chem 46: 2436-45 (2003) Article DOI: 10.1021/jm020517g BindingDB Entry DOI: 10.7270/Q2154GFS
					More data for this Ligand-Target Pair