BDBM50350367 CHEMBL1813116

SMILES: CN1C[C@@H](COc2ccc(cc2)C(=O)n2c(C)c(CC(O)=O)c3cc(C)ccc23)Oc2ccccc12

InChI Key: InChIKey=JMJJALVWBXMBRZ-UHFFFAOYSA-N

Data: 8 KI  1 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 9 hits for monomerid = 50350367   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Prostaglandin D2 receptor (Mouse)	BDBM50350367 (CHEMBL1813116) Show SMILES Show InChI	GoogleScholar	UniChem		n/a	n/a	4.30	n/a	n/a	n/a	n/a	n/a	n/a
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Prostaglandin D2 receptor (Mouse)	BDBM50350367 (CHEMBL1813116) Show SMILES Show InChI	GoogleScholar	UniChem		28	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
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Prostaglandin E2 receptor EP2 subtype (Mouse)	BDBM50350367 (CHEMBL1813116) Show SMILES Show InChI	GoogleScholar	UniChem		340	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
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Prostacyclin receptor (Human)	BDBM50350367 (CHEMBL1813116) Show SMILES Show InChI	GoogleScholar	UniChem		1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
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Prostaglandin F2-alpha receptor (Mouse)	BDBM50350367 (CHEMBL1813116) Show SMILES Show InChI	GoogleScholar	UniChem		1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
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Prostaglandin E2 receptor EP3 subtype (Mouse)	BDBM50350367 (CHEMBL1813116) Show SMILES Show InChI	GoogleScholar	UniChem		2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
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Prostaglandin E2 receptor EP4 subtype (Mouse)	BDBM50350367 (CHEMBL1813116) Show SMILES Show InChI	GoogleScholar	UniChem		3.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
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Prostaglandin E2 receptor EP1 subtype (Mouse)	BDBM50350367 (CHEMBL1813116) Show SMILES Show InChI	GoogleScholar	UniChem		5.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
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Thromboxane A2 receptor (Human)	BDBM50350367 (CHEMBL1813116) Show SMILES Show InChI	GoogleScholar	UniChem		>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
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