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Lapachol

Cat. No. M17443
Lapachol Structure
Size Price Availability Quantity
5mg USD 32  USD32 In stock
10mg USD 50  USD50 In stock
50mg USD 100  USD100 In stock
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Quality Control & Documentation
Biological Activity

Lapachol is a naturally occurring naphthoquinone and orally active, potent inhibitor of dihydroorotic acid dehydrogenase (DHODH).Lapachol has immunosuppressive activity against lymphocytes by inhibiting pyrimidine synthesis through direct blockade of DHODH activity. In addition, Lapachol is a vitamin K antagonist with antitumor and antileishmanial activity that inhibits DNA and RNA synthesis in tumor cells.

Chemical Information
Molecular Weight 242.00
Formula C15H14O3
CAS Number 84-79-7
Form Solid
Solubility (25°C) DMSO 66.67 mg/mL
Storage 4°C
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Shaheen Bibi, et al. Iran J Pharm Res. Lapachol-Induced Upregulation of Sirt1/Sirt3 is linked with Improved Skin Wound Healing in Alloxan-induced Diabetic Mice

[2] Jaeryeon Kim, et al. Curr Mol Pharmacol. Effect of Lapachol on the Inhibition of Matrix Metalloproteinase Related to the Invasion of Human Fibrosarcoma Cells

[3] Nico Linzner, et al. Free Radic Biol Med. The plant-derived naphthoquinone lapachol causes an oxidative stress response in Staphylococcus aureus

[4] Lucas Bonfim Marques, et al. Toxicol In Vitro. Lapachol acetylglycosylation enhances its cytotoxic and pro-apoptotic activities in HL60 cells

[5] Hidayat Hussain, et al. Expert Opin Ther Pat. Lapachol and lapachone analogs: a journey of two decades of patent research(1997-2016)

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