BDBM50411165 CHEMBL215360

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](OCCCO)[C@H](O)C2=C)OC(=O)C1=C

InChI Key: InChIKey=ANMDQTCGJNGDBJ-PMDCVXGBSA-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 = 50411165   

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))	BDBM50411165 (CHEMBL215360) 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](OCCCO)[C@H](O)C2=C)OC(=O)C1=C Show InChI InChI=1S/C33H50O6/c1-6-9-25-22(4)32(37)39-29(25)18-20(2)26-13-14-27-23(10-7-15-33(26,27)5)11-12-24-19-28(35)31(30(36)21(24)3)38-17-8-16-34/h11-12,20,25-31,34-36H,3-4,6-10,13-19H2,1-2,5H3/b23-11+,24-12-/t20-,25+,26-,27+,28-,29-,30-,31+,33-/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