BDBM36104 (R)-2-phenylpropionic acid

SMILES: C[C@@H](C([O-])=O)c1ccccc1

InChI Key: InChIKey=YPGCWEMNNLXISK-SSDOTTSWSA-M

Data: 1 IC50  1 ITC

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 1 hit for monomerid = 36104   

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
Fatty-acid amide hydrolase 1 (Homo sapiens (Human))	BDBM36104 ((R)-2-phenylpropionic acid) Show SMILES C[C@@H](C([O-])=O)c1ccccc1 Show InChI InChI=1S/C9H10O2/c1-7(9(10)11)8-5-3-2-4-6-8/h2-7H,1H3,(H,10,11)/p-1/t7-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.23E+6	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ catholique de Louvain Curated by ChEMBL					Assay Description Inhibition of human recombinant FAAH				Eur J Med Chem 45: 3564-74 (2010) Article DOI: 10.1016/j.ejmech.2010.04.040 BindingDB Entry DOI: 10.7270/Q23J3F68
					More data for this Ligand-Target Pair

Activity Spreadsheet -- ITC Data from BindingDB

Found 1 hit for monomerid = 36104

Cell (A)	Syringe (B)	Cell Links	Syringe Links	Cell + Syr Links	ΔG° kcal/mole	-TΔS° kcal/mole	ΔH° kcal/mole	log K	pH	Temp °C
BDBM11	BDBM36104	CHEBI KEGG MMDB PC cid PC sid PDB	CHEBI PC cid PC sid		-2.09	0.0214	-2.10	1.53	6.90	25
Japan Science and Technology Agency					J Am Chem Soc 122: 4418-35 (2000)