BDBM50219341 CHEMBL70208

SMILES: CNC(=O)CC[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1

InChI Key: InChIKey=LKHQKJYBQSVJAX-SFTDATJTSA-N

Data: 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 1 hit for monomerid = 50219341   

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
C-C chemokine receptor type 1 (Homo sapiens (Human))	BDBM50219341 (CHEMBL70208) Show SMILES CNC(=O)CC[C@H](O)[C@H](CC1CCCCC1)NC(=O)c1cnc2ccccc2c1 Show InChI InChI=1S/C23H31N3O3/c1-24-22(28)12-11-21(27)20(13-16-7-3-2-4-8-16)26-23(29)18-14-17-9-5-6-10-19(17)25-15-18/h5-6,9-10,14-16,20-21,27H,2-4,7-8,11-13H2,1H3,(H,24,28)(H,26,29)/t20-,21-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	<5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Compound was tested for inhibition of CCL3 binding to chemokine receptor-1; inactive at a concentration of 32 uM				Bioorg Med Chem Lett 14: 2163-7 (2004) Article DOI: 10.1016/j.bmcl.2004.02.020 BindingDB Entry DOI: 10.7270/Q2CV4H5M
					More data for this Ligand-Target Pair