LY2562175
Selleck Chemicals
SKU:S0403-5MG
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LY2562175 is an agonist of FXR used in studies of Hormone Signaling and Metabolic Signaling. It is especially relevant when investigators need a named chemical input and interpretable readouts connected to ligand-dependent transcriptional programs and endocrine regulation and metabolic regulation, energy sensing, and enzyme-linked homeostasis in endocrinology and metabolism models.
By activating FXR, LY2562175 can be used to examine ligand-dependent transcriptional programs and endocrine regulation and metabolic regulation, energy sensing, and enzyme-linked homeostasis. The nuclear receptor annotation adds relevance to reporter-gene, receptor-binding, and transcriptional assays, together with downstream-response mapping in the same experimental setting. In endocrinology and metabolism models, these readouts can be combined with viability, reporter, localization, biochemical conversion, or morphology endpoints to refine experimental interpretation.
Research Applications
- Target-focused assays involving FXR
- Pathway perturbation studies connected to Hormone Signaling and Metabolic Signaling
- Agonist-response and downstream signaling studies
- Reporter-gene, receptor-binding, and transcriptional assays
Overall, LY2562175 is appropriate when a defined chemical perturbant is needed to connect FXR with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in endocrinology and metabolism models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.
- Targets:
- FXR
- Target Class:
- Nuclear Receptor
- Pathways:
- Hormone Signaling • Metabolic Signaling
- Research Area:
- Endocrinology • Metabolism
- CAS No.:
- 1103500-20-4
- Molecular Weight:
- 540.44
- Formula:
- C₂₈H₂₇Cl₂N₃O₄
- SMILES:
- CN1C=C(C2=C1C=C(C=C2)N3CCC(CC3)OCC4=C(ON=C4C5=C(C=CC=C5Cl)Cl)C6CC6)C(=O)O
- Storage Temperature:
- -20°C
For Research Use Only. Not intended for diagnostic or therapeutic use.
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