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Beta-Lapachone

DNA topoisomerase I inhibitor

Product Specifications

Background

β-Lapachone is a naturally occurring quinone obtained from the bark of the lapacho tree (Tabebuia avellanedae) with cancer chemopreventive properties. A novel DNA topoisomerase I inhibitor which unlike camptothecin does not stabilize the cleavable complex indicating a novel mode of action (1). Induces apoptosis in a number of cancer cell lines (2). In cancer cells overexpressing NAD(P)H:quinone oxidoreductase, reduction of β-lapachone leads to futile cycling between quinone and hydroquinone forms (3) resulting in the production of reactive oxygen species (4). Suppresses radiation-induced activation of NFĸB (5). Attenuates cognitive impairment and inflammation in amyloid-induced mouse model.

CAS Number

4707-32-8

Product Name Alternative

3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran-5,6-dione; NSC-26326

UNSPSC

41116105

Type

Inhibitor

Source

Synthetic

Field of Research

Cell Signaling | Epigenetics and Nuclear Signaling | DNA/RNA | DNA Synthesis | Topoisomerases | Neuroscience | Neurodegeneration | Alzheimer's Disease

Purity

>98% (HPLC) ; NMR (Conforms)

Weight

0.005

Format

Orange powder

Solubility

May be dissolved in DMSO (35 mg/ml); or Ethanol (15 mg/ml)

Molecular Formula

C15H14O3

Molecular Weight

242.3

Precautions

Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.

References & Citations

1. CJ Li et al. J. Biol. Chem. 1993 268:22463 2. SM Wuerzberger et al. Cancer Res. 1998 58:1876 3. JJ Pink et al. J. Biol. Chem. 2000 275:5416 4. D Siegel et al. Biochem. Pharmacol. 2012 83:1033 5. GZ Dong et al. Exp. Mol. Med. 2010 42:327
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