null
SMILES [H][C@](O)(CCC(C)C)[C@@H](C)[C@@]1([H])CC[C@@]2([H])[C@]3([H])CC=C4C[C@@]([H])(O)CC[C@]4(C)[C@@]3([H])CC[C@]12C
InChI Key InChIKey=RZPAXNJLEKLXNO-QUOSNDFLSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 20176
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Lilly Research Laboratories
Curated by PDSP Ki Database
Lilly Research Laboratories
Curated by PDSP Ki Database
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
Lilly Research Laboratories
Curated by PDSP Ki Database
Lilly Research Laboratories
Curated by PDSP Ki Database
TargetNPC1-like intracellular cholesterol transporter 1(Homo sapiens (Human))
The University of Tokyo
Curated by ChEMBL
The University of Tokyo
Curated by ChEMBL
Affinity DataEC50: 2.90E+3nMAssay Description:Binding affinity to FLAG/tGFP-tagged NPC1 I1061T mutant (unknown origin) expressed in HEK293 cells assessed as localization after 24 hrs by fluoresce...More data for this Ligand-Target Pair
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
Lilly Research Laboratories
Curated by PDSP Ki Database
Lilly Research Laboratories
Curated by PDSP Ki Database
Affinity DatapH: 7.5 T: 2°CAssay Description:The LXR LiSA measures the ligand-dependent recruitment of a 25 amino acid fragment of the steroid receptor coactivator 1 (SRC1) to the ligand-binding...More data for this Ligand-Target Pair