LXR-623 | Partial Agonist of NR1H2, NR1H3
RATINGS:
Cellular Use: (2 reviews)

In Model Organisms: (1 reviews)
Control Compounds

Probe Summary

Targets Biochemical/Biophysical Potency Cellular Potency
NR1H2
  • IC 50:179 nM
  • EC50 , (% effect):GAL4 LXRα 6.66 uM (53)
NR1H3
  • IC 50:24 nM
  • EC50 , (% effect):GAL4 LXRβ 3.67 uM (73); GAL4 LXRα 6.66 uM (53); ABAC1 0.53 uM (100); C-Efflux 1.27 uM (140); SREBP1 2.11 uM (58); Lipid acc. 1.91 uM (35)
Partial Agonist
up to 2 uM

Selectivity

In Cell Selectivity Assessment
Selectivity Assessment Description:
PPAR and FXR Gal4 transactivation assays show no agonist effects for PPARα, PPARγ, PPARδ and FXR. Bi ...

Potency
Cellular
In Vitro

NR1H2

Mode of Action: Partial Agonist

Structure-Activity-Relationship data available? Yes

DOI Reference: 10.1021/jm800799q

NR1H3

Mode of Action: Partial Agonist

Structure-Activity-Relationship data available? No

DOI Reference: 10.1021/jm800799q

In Vivo Validations

Mouse, Rat, Hamster, Cynomolgus, Rabbit
Dose: 30 (r), 50 (m) mg/kg/day, 15, 50 mg/Kg (R), 20, 60, and 120 mg/kg/day (ham), 50 mg/Kg (mon)Rab
Route of delivery: Oral
Organ of interest (O): Liver, Brain

DOI Reference: 10.1021/jm800799q

Orthogonal Probes def

TO901317
GSK2033
SR9238

Chemical Information

Molecular Formula C21H12ClF5N2
SMILEs Fc1ccc(-c2c3cccc(C(F)(F)F)c3nn2Cc2ccc(F)cc2Cl)cc1
InChI InChI=1S/C21H12ClF5N2/c22-18-10-15(24)9-6-13(18)11-29-20(12-4-7-14(23)8-5-12)16-2-1-3-17(19(16)28-29)21(25,26)27/h1-10H,11H2
Molecular weight 422.06 Da
AlogP 6.702000000000003
HBond acceptors 2
HBond donors --
Atoms 41

References

Publications

Cross References

Vendors

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Expert Reviews


(on 10 Nov 2020 )
Cellular Use Rating
This compound is a partial agonist of LXRa making interpretation of its biology in cells very complex. Partial agonists of nuclear receptors do not make good chemical probes. I do not recommend use...
(on 16 Nov 2020 )
Cellular Use Rating
In Model Organisms
( The reviewer did not leave any comments )
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