CAS No. 1161002-05-6

Batch: Purity:99.35
G15 Chemical Structure
Chemical Structure
Check the G15 product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name (3aS,4R,9bR)-4-(6-bromo-1,3-benzodioxol-5-yl)-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline
CAS Number 1161002-05-6
Molecular Formula

C19H16BrNO2

Molecular Weight (MW) 370.24
SMILES C1C=CC2C1C(NC3=CC=CC=C23)C4=CC5=C(C=C4Br)OCO5
InChIKey YOLTZIVRJAPVPH-MJLGCCKJSA-N

Ordering Information

Biological Activity

G15 is a cell-permeable and selective G-protein coupled estrogen receptor (GPER/GPR30) antagonist with a binding affinity of approximately, showing no affinity for ERα or ERβ at concentrations up to. By blocking GPER, G15 inhibits downstream estrogen-stimulated signal transduction, including ERK phosphorylation and intracellular calcium mobilization. This inhibition suppresses estrogen-mediated cell proliferation and physiological cellular responses. [1]

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 74 mg/mL (199.87 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.