BDBM50468000 CHEMBL4288251

SMILES: [H][C@@]12CC(CCCCCCCCCC(O)=O)=C(c3ccccc3)[C@@]1(CC[C@H]2O)C(=C)c1ccccc1

InChI Key: InChIKey=YGTFMMNUBBGVSN-LBRLCBGXSA-N

Data: 1 EC50

PDB links: 1 PDB ID matches this monomer.

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 = 50468000   

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
Liver Receptor Homolog 1 (Homo sapiens (Human))	BDBM50468000 (CHEMBL4288251) Show SMILES [H][C@@]12CC(CCCCCCCCCC(O)=O)=C(c3ccccc3)[C@@]1(CC[C@H]2O)C(=C)c1ccccc1 |r,t:15| Show InChI InChI=1S/C32H40O3/c1-24(25-15-10-7-11-16-25)32-22-21-29(33)28(32)23-27(31(32)26-17-12-8-13-18-26)19-9-5-3-2-4-6-14-20-30(34)35/h7-8,10-13,15-18,28-29,33H,1-6,9,14,19-23H2,(H,34,35)/t28-,29+,32-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	PDB Article PubMed	n/a	n/a	n/a	n/a	400	n/a	n/a	n/a	n/a
Emory University Curated by ChEMBL					Assay Description Agonist activity at recombinant full length human LRH1 expressed in HeLa cells after 24 hrs by dual-glo luciferase reporter gene assay				ACS Med Chem Lett 9: 1051-1056 (2018) Article DOI: 10.1021/acsmedchemlett.8b00361 BindingDB Entry DOI: 10.7270/Q2WW7MCP
					More data for this Ligand-Target Pair				3D Structure (crystal)