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β-Lapachone, a novel topoisomerase I (Topo I) inhibitor, does not stabilize the cleavable complex indicating a novel mode of action, unlike camptothecin (sc-200871). The compound exhibits the ability to induce apoptosis in various cell lines, such as prostate cancer and promyelocytic leukemia cells. It functions by blocking the cell cycle at the G0/G1 phase. Additionally, it exerts effects on DNA topoisomerase II, NF-κB, AP-1, and JNK signaling pathways.
Ordering Information
Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
β-Lapachone, 5 mg | sc-200875 | 5 mg | $110.00 | |||
US: Only available in the US | ||||||
β-Lapachone, 25 mg | sc-200875A | 25 mg | $450.00 | |||
US: Only available in the US |