CAS No. 142878-12-4

Batch: Purity:97.65
U-73343 Chemical Structure
Chemical Structure
Check the U-73343 product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name 1-[6-[[(8R,9S,13S,14S,17S)-3-methoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]amino]hexyl]pyrrolidine-2,5-dione
CAS Number 142878-12-4
Molecular Formula

C29H42N2O3

Molecular Weight (MW) 466.66
InChIKey CJHWFIUASFBCKN-ZRJUGLEFSA-N

Ordering Information

Biological Activity

U-73343 is an aminosteroid derivative and inactive analog of U-73122 that acts downstream of phospholipase C without inhibiting its enzymatic activity. In cellular models, U-73343 inhibits receptor-mediated phospholipase D activation and modulates lipid second messenger signaling. Additionally, U-73343 acts as an agonist of nuclear estrogen receptors alpha and beta, driving estrogen receptor-dependent transcriptional activity and downstream 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 7 mg/mL (15.0 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Ethanol 2 mg/mL
Water 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.