BDBM50411128 CHEMBL215806

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

InChI Key: InChIKey=XHGINMPRHPSKTP-MJDLTQARSA-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 = 50411128   

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))	BDBM50411128 (CHEMBL215806) Show SMILES C[C@H](C[C@@H]1OC(=O)C(=C)[C@H]1C)[C@H]1CC[C@H]2\C(CCC[C@]12C)=C\C=C1\C[C@@H](O)[C@H](C)[C@H](O)C1=C Show InChI InChI=1S/C29H42O4/c1-16(14-26-17(2)18(3)28(32)33-26)23-11-12-24-21(8-7-13-29(23,24)6)9-10-22-15-25(30)20(5)27(31)19(22)4/h9-10,16-17,20,23-27,30-31H,3-4,7-8,11-15H2,1-2,5-6H3/b21-9+,22-10-/t16-,17-,20+,23-,24+,25-,26+,27-,29-/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	6.80	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