BDBM50240684 CHEMBL1309685

SMILES: COc1cc(OC)c2c(cc(=O)oc2c1C(CC(=O)N1CCCC1)c1ccc2OCOc2c1)-c1ccccc1

InChI Key: InChIKey=TVEPKCACBQNJDB-UHFFFAOYSA-N

Data: 2 KI  2 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 4 hits for monomerid = 50240684   

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
ELAV-like protein 1 (Homo sapiens (Human))	BDBM50240684 (CHEMBL1309685) Show SMILES COc1cc(OC)c2c(cc(=O)oc2c1C(CC(=O)N1CCCC1)c1ccc2OCOc2c1)-c1ccccc1 Show InChI InChI=1S/C31H29NO7/c1-35-25-17-26(36-2)30-22(19-8-4-3-5-9-19)16-28(34)39-31(30)29(25)21(15-27(33)32-12-6-7-13-32)20-10-11-23-24(14-20)38-18-37-23/h3-5,8-11,14,16-17,21H,6-7,12-13,15,18H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.05E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Pavia Curated by ChEMBL					Assay Description Inhibition of ELAV1 (unknown origin)-ARE sequence of Mushashi1 transcript complex formation after 2 hrs by fluorescence polarization assay				J Med Chem 60: 8257-8267 (2017) Article DOI: 10.1021/acs.jmedchem.6b01871 BindingDB Entry DOI: 10.7270/Q2377BWD
					More data for this Ligand-Target Pair
ELAV-like protein 1 (Homo sapiens (Human))	BDBM50240684 (CHEMBL1309685) Show SMILES COc1cc(OC)c2c(cc(=O)oc2c1C(CC(=O)N1CCCC1)c1ccc2OCOc2c1)-c1ccccc1 Show InChI InChI=1S/C31H29NO7/c1-35-25-17-26(36-2)30-22(19-8-4-3-5-9-19)16-28(34)39-31(30)29(25)21(15-27(33)32-12-6-7-13-32)20-10-11-23-24(14-20)38-18-37-23/h3-5,8-11,14,16-17,21H,6-7,12-13,15,18H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	6.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Pavia Curated by ChEMBL					Assay Description Inhibition of ELAV1 RRM1/RRM2 domains (unknown origin) interaction with ARE sequence of Mushashi1 transcript after 2 hrs by AlphaLISA method				J Med Chem 60: 8257-8267 (2017) Article DOI: 10.1021/acs.jmedchem.6b01871 BindingDB Entry DOI: 10.7270/Q2377BWD
					More data for this Ligand-Target Pair
ELAV-like protein 1 (Homo sapiens (Human))	BDBM50240684 (CHEMBL1309685) Show SMILES COc1cc(OC)c2c(cc(=O)oc2c1C(CC(=O)N1CCCC1)c1ccc2OCOc2c1)-c1ccccc1 Show InChI InChI=1S/C31H29NO7/c1-35-25-17-26(36-2)30-22(19-8-4-3-5-9-19)16-28(34)39-31(30)29(25)21(15-27(33)32-12-6-7-13-32)20-10-11-23-24(14-20)38-18-37-23/h3-5,8-11,14,16-17,21H,6-7,12-13,15,18H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.65E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Pavia Curated by ChEMBL					Assay Description Inhibition of ELAV1 RRM1/RRM2 domains (unknown origin) interaction with ARE sequence of Mushashi1 transcript after 2 hrs by AlphaLISA method				J Med Chem 60: 8257-8267 (2017) Article DOI: 10.1021/acs.jmedchem.6b01871 BindingDB Entry DOI: 10.7270/Q2377BWD
					More data for this Ligand-Target Pair
ELAV-like protein 1 (Homo sapiens (Human))	BDBM50240684 (CHEMBL1309685) Show SMILES COc1cc(OC)c2c(cc(=O)oc2c1C(CC(=O)N1CCCC1)c1ccc2OCOc2c1)-c1ccccc1 Show InChI InChI=1S/C31H29NO7/c1-35-25-17-26(36-2)30-22(19-8-4-3-5-9-19)16-28(34)39-31(30)29(25)21(15-27(33)32-12-6-7-13-32)20-10-11-23-24(14-20)38-18-37-23/h3-5,8-11,14,16-17,21H,6-7,12-13,15,18H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Pavia Curated by ChEMBL					Assay Description Inhibition of ELAV1 (unknown origin)-ARE sequence of Mushashi1 transcript complex formation after 2 hrs by fluorescence polarization assay				J Med Chem 60: 8257-8267 (2017) Article DOI: 10.1021/acs.jmedchem.6b01871 BindingDB Entry DOI: 10.7270/Q2377BWD
					More data for this Ligand-Target Pair