CAS No. 66611-37-8

Batch: Purity:99.94
BGP-15 2HCl Chemical Structure
Chemical Structure
Check the BGP-15 2HCl product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name N'-(2-hydroxy-3-piperidin-1-ylpropoxy)pyridine-3-carboximidamide;dihydrochloride
CAS Number 66611-37-8
Molecular Formula

C14H22N4O2.2HCl

Molecular Weight (MW) 351.27
SMILES C1CCN(CC1)CC(CON=C(C2=CN=CC=C2)N)O.Cl.Cl
InChIKey ISGGVCWFTPTHIX-UHFFFAOYSA-N

Ordering Information

Biological Activity

BGP-15 2HCl is a nicotinic amidoxime derivative that acts as a poly(ADP-ribose) polymerase (PARP) inhibitor and chaperone co-inducer. By modulating PARP activity and upregulating heat shock protein signaling, it attenuates oxidative stress, preserves mitochondrial integrity, and reduces cell death during cellular stress. Downstream, these pathway alterations contribute to cell survival and protect tissues against ischemia-reperfusion injury in preclinical models. [1][2]

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 70 mg/mL (199.27 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Water 70 mg/mL
Ethanol 70 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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Note: Technical data last updated: Sep 1, 2026.