CAS No. 2102933-95-7

Batch: Purity:99.78
GSK-LSD1 2HCl Chemical Structure
Chemical Structure
Check the GSK-LSD1 2HCl product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name N-[(1R,2S)-2-phenylcyclopropyl]piperidin-4-amine;dihydrochloride
CAS Number 2102933-95-7
Molecular Formula

C14H22Cl2N2

Molecular Weight (MW) 289.24
SMILES C1CNCCC1NC2CC2C3=CC=CC=C3.Cl.Cl
InChIKey PJFZOGMSPBHPNS-WICJZZOFSA-N

Biological Activity

GSK-LSD1 2HCl is an irreversible, selective lysine-specific demethylase 1 (LSD1) inhibitor with an IC50 of, displaying >1000-fold selectivity over LSD2, MAO-A, and MAO-B. Inhibition of LSD1 blocks demethylation of histone H3 lysine 4 (H3K4), leading to altered gene expression. This blockade suppresses cell proliferation and promotes differentiation in acute myeloid leukemia and small cell lung cancer models. [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 57 mg/mL (197.06 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Water 57 mg/mL
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).
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Reference

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Note: Technical data last updated: Sep 1, 2026.