EUB0001065a_NR1B3

Chemical structure of compound EUB0001065a
Compound name
AC-261066
Protein family
Nuclear Receptors
Target name
NR1B3
Affinity on-target cellular (nM)
501
CG-Set
Nuclear Receptor set
Recommended Concentration
1 µM
Compound EUbOPEN ID
EUB0001065a
SMILES
CCCCOCCOC1=C(SC(=N1)C2=CC(=C(C=C2)C(=O)O)F)C
InChIKey
HSAOETBFVAWNRP-UHFFFAOYSA-N
Mode of action
Agonist
Affinity on-target cellular definition
EC50
Affinity on-target cellular assay type
Cell-based R-SAT assay (NIH3T3 fibroblasts are transfected in presence of a RAR?, RAR? or RAR? receptor and ?-galactosidase expression vectors and vectors encoding various signaling molecules)
Affinity on-target cellular source knowledge
https://doi.org/10.1021/jm801532e
https://doi.org/10.1021/jm050891r
Affinity on-target cellular relation
0
Selectivity platform
Nuclear receptor panel, bromodomain and kinase panel
Selectivity platform number of targets
20
Selectivity remarks
Screened at 1 µM against NR2A1, NR2B1, NR2C1, NR2E1, NR4A1, NR5A1 and VP16 in a Gal4 hybrid reporter gene assay (HEK293T cells were cotransfected with pFR-Luc reporter, pRL-SV40 control reporter and pFA-CMV containing the Gal4-DBD fused with human NR-LBD of interest or pECE-SV40-Gal4-VP16): fold-activation = 25.62 (NR2B1); Screened at 20 µM in a bromodomain and kinase panel against ABL1, AURKA, BRD4, BRPF1, CDK2, CSNK1D, FGFR3, GSK3B, MAPK1, TRIM24 in DSF assays: clean selectivity profile with no significant binding (?Tm < 2 K)
Selectivity Number of Off-targets
1