BDBM50427289 CHEMBL2325424

SMILES: Cc1ccc(cc1)C(CCC(N)C(O)=O)(c1ccccc1)c1cccc(O)c1

InChI Key: InChIKey=IWSYHPMWULTFDC-UHFFFAOYSA-N

Data: 1 KI

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 = 50427289   

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
Kinesin-like protein 1 (Homo sapiens (Human))	BDBM50427289 (CHEMBL2325424) Show SMILES Cc1ccc(cc1)C(CCC(N)C(O)=O)(c1ccccc1)c1cccc(O)c1 Show InChI InChI=1S/C24H25NO3/c1-17-10-12-19(13-11-17)24(15-14-22(25)23(27)28,18-6-3-2-4-7-18)20-8-5-9-21(26)16-20/h2-13,16,22,26H,14-15,25H2,1H3,(H,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Beatson Institute for Cancer Research Curated by ChEMBL					Assay Description Inhibition of human N-terminal His6-tagged Eg5 (1 to 368 amino acid residues) motor domain basal ATPase activity expressed in Escherichia coli BL21 (...				J Med Chem 56: 1878-93 (2013) Article DOI: 10.1021/jm3014597 BindingDB Entry DOI: 10.7270/Q20866NN
					More data for this Ligand-Target Pair