BDBM50411106 CHEMBL387098

SMILES: C[C@H](C[C@H]1OC(=O)C(=C)C11CCCC1)[C@H]1CC[C@H]2\C(CCC[C@]12C)=C\C=C1\C[C@@H](O)C[C@H](O)C1=C

InChI Key: InChIKey=LLJYGIMZMSGNRD-YTJYPAFVSA-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 = 50411106   

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
Vitamin D3 receptor (Homo sapiens (Human))	BDBM50411106 (CHEMBL387098) Show SMILES C[C@H](C[C@H]1OC(=O)C(=C)C11CCCC1)[C@H]1CC[C@H]2\C(CCC[C@]12C)=C\C=C1\C[C@@H](O)C[C@H](O)C1=C Show InChI InChI=1S/C31H44O4/c1-19(16-28-31(14-5-6-15-31)21(3)29(34)35-28)25-11-12-26-22(8-7-13-30(25,26)4)9-10-23-17-24(32)18-27(33)20(23)2/h9-10,19,24-28,32-33H,2-3,5-8,11-18H2,1,4H3/b22-9+,23-10-/t19-,24-,25-,26+,27+,28-,30-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
Teikyo University Curated by ChEMBL					Assay Description Antagonist activity against 1-alpha,25-dihydroxy vitamin D3-induced HL60 cell differentiation by NBT reduction method				J Med Chem 49: 7063-75 (2006) Article DOI: 10.1021/jm060797q BindingDB Entry DOI: 10.7270/Q2F47QC9
					More data for this Ligand-Target Pair