CAS No. 1227634-69-6

Batch: Purity:99.81
GNF351 Chemical Structure
Chemical Structure
Check the GNF351 product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name N-[2-(1H-indol-3-yl)ethyl]-2-(5-methyl-3-pyridinyl)-9-propan-2-ylpurin-6-amine
CAS Number 1227634-69-6
Molecular Formula

C24H25N7

Molecular Weight (MW) 411.50
SMILES CC(C)[N]1C=NC2=C1N=C(N=C2NCCC3=C[NH]C4=C3C=CC=C4)C5=CC(=CN=C5)C
InChIKey ABXIUYMKZDZUDC-UHFFFAOYSA-N

Ordering Information

Biological Activity

GNF351 is a potent antagonist of the aryl hydrocarbon receptor (AHR) that competes for binding to the AHR ligand-binding pocket with an IC50 of 62 nM. By blocking AHR activation, GNF351 inhibits AHR nuclear translocation, DNA binding, and the transcriptional expression of downstream target genes such as CYP1A1. Consequently, this inhibition suppresses ligand-induced AHR signaling pathways involved in xenobiotic metabolism, cellular differentiation, and immune response regulation.

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
DMSO 30 mg/mL (72.9 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Water Insoluble
Ethanol Insoluble
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).
Note: Technical data last updated: Sep 1, 2026.