BDBM50411136 CHEMBL385926

SMILES: CCC[C@H]1[C@@H](C[C@@H](C)[C@H]2CC[C@H]3\C(CCC[C@]23C)=C\C=C2\C[C@@H](O)[C@H](C)[C@H](O)C2=C)OC(=O)C1=C

InChI Key: InChIKey=VQVQNWPFJVCLCY-AAJZEELKSA-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 = 50411136   

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))	BDBM50411136 (CHEMBL385926) Show SMILES CCC[C@H]1[C@@H](C[C@@H](C)[C@H]2CC[C@H]3\C(CCC[C@]23C)=C\C=C2\C[C@@H](O)[C@H](C)[C@H](O)C2=C)OC(=O)C1=C Show InChI InChI=1S/C31H46O4/c1-7-9-24-20(4)30(34)35-28(24)16-18(2)25-13-14-26-22(10-8-15-31(25,26)6)11-12-23-17-27(32)21(5)29(33)19(23)3/h11-12,18,21,24-29,32-33H,3-4,7-10,13-17H2,1-2,5-6H3/b22-11+,23-12-/t18-,21+,24-,25-,26+,27-,28-,29-,31-/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	6.30	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