BDBM50424977 CHEMBL2316784

SMILES: COc1ccc(cc1)-c1csc(n1)N1N=C(CC1c1ccc2OCCOc2c1)c1ccc(Br)cc1

InChI Key: InChIKey=NEOSQRVTGAPRQV-UHFFFAOYSA-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 = 50424977   

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
Receptor tyrosine-protein kinase erbB-2 (Homo sapiens (Human))	BDBM50424977 (CHEMBL2316784) Show SMILES COc1ccc(cc1)-c1csc(n1)N1N=C(CC1c1ccc2OCCOc2c1)c1ccc(Br)cc1 |c:16| Show InChI InChI=1S/C27H22BrN3O3S/c1-32-21-9-4-18(5-10-21)23-16-35-27(29-23)31-24(15-22(30-31)17-2-7-20(28)8-3-17)19-6-11-25-26(14-19)34-13-12-33-25/h2-11,14,16,24H,12-13,15H2,1H3	PDB MMDB UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.32E+3	n/a	n/a	n/a	n/a	n/a	n/a
Nanjing University Curated by ChEMBL					Assay Description Inhibition of human HER2 cytoplasmic domain (amino acids 676 to 1245) expressed in Sf9 cells by DELFIA time resolved fluorometry				Bioorg Med Chem 21: 448-55 (2012) Article DOI: 10.1016/j.bmc.2012.11.020 BindingDB Entry DOI: 10.7270/Q2NS0W7B
					More data for this Ligand-Target Pair