BDBM50025953 6-Imidazo[1,5-a]pyridin-5-yl-hexanoic acid::CGS-13080::CHEMBL48092

SMILES: OC(=O)CCCCCc1cccc2cncn12

InChI Key: InChIKey=LIFOFTJHFFTNRV-UHFFFAOYSA-N

Data: 4 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 4 hits for monomerid = 50025953   

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
Thromboxane A2 Synthase (P450 TxA2) (Homo sapiens (Human))	BDBM50025953 (6-Imidazo[1,5-a]pyridin-5-yl-hexanoic acid | CGS-1...) Show SMILES OC(=O)CCCCCc1cccc2cncn12 Show InChI InChI=1S/C13H16N2O2/c16-13(17)8-3-1-2-5-11-6-4-7-12-9-14-10-15(11)12/h4,6-7,9-10H,1-3,5,8H2,(H,16,17)	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibition of thromboxane synthase				Bioorg Med Chem Lett 4: 2067-2072 (1994) Article DOI: 10.1016/S0960-894X(01)80103-7 BindingDB Entry DOI: 10.7270/Q2GX4BG6
					More data for this Ligand-Target Pair
Cyclooxygenase (Homo sapiens (Human))	BDBM50025953 (6-Imidazo[1,5-a]pyridin-5-yl-hexanoic acid | CGS-1...) Show SMILES OC(=O)CCCCCc1cccc2cncn12 Show InChI InChI=1S/C13H16N2O2/c16-13(17)8-3-1-2-5-11-6-4-7-12-9-14-10-15(11)12/h4,6-7,9-10H,1-3,5,8H2,(H,16,17)	PDB KEGG UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibitory activity against Prostaglandin G/H synthase				J Med Chem 28: 164-70 (1985) BindingDB Entry DOI: 10.7270/Q22B8ZKX
					More data for this Ligand-Target Pair
Prostaglandin I2 synthase (Homo sapiens (Human))	BDBM50025953 (6-Imidazo[1,5-a]pyridin-5-yl-hexanoic acid | CGS-1...) Show SMILES OC(=O)CCCCCc1cccc2cncn12 Show InChI InChI=1S/C13H16N2O2/c16-13(17)8-3-1-2-5-11-6-4-7-12-9-14-10-15(11)12/h4,6-7,9-10H,1-3,5,8H2,(H,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibitory activity against prostacyclin synthetase				J Med Chem 28: 164-70 (1985) BindingDB Entry DOI: 10.7270/Q22B8ZKX
					More data for this Ligand-Target Pair
Thromboxane A2 Synthase (P450 TxA2) (Homo sapiens (Human))	BDBM50025953 (6-Imidazo[1,5-a]pyridin-5-yl-hexanoic acid | CGS-1...) Show SMILES OC(=O)CCCCCc1cccc2cncn12 Show InChI InChI=1S/C13H16N2O2/c16-13(17)8-3-1-2-5-11-6-4-7-12-9-14-10-15(11)12/h4,6-7,9-10H,1-3,5,8H2,(H,16,17)	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.20	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro inhibitory activity against thromboxane A2 synthetase with lysed human platelets as the enzyme source.				J Med Chem 28: 164-70 (1985) BindingDB Entry DOI: 10.7270/Q22B8ZKX
					More data for this Ligand-Target Pair