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PRL-3 Inhibitor I

Cat. No. M7996
PRL-3 Inhibitor I Structure
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Biological Activity

PRL-3 Inhibitor I is a rhodanine derivative with an IC50 value of 0.9 μM against phosphatase of regenerating liver-3 (PRL-3), a nonclassical protein tyrosine phosphatase that has recently been shown to be involved in cancer metastasis. PRL-3 Inhibitor I reduced the invasiveness of B16F10 melanoma cells in a cell based assay.

Chemical Information
Molecular Weight 485.21
Formula C17H11Br2NO2S2
CAS Number 893449-38-2
Solubility (25°C) DMSO: ≥10 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
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] Xiaomin Chen, et al. The combination of PRL-3 inhibitor with sorafenib synergistically promotes AML apoptosis

[2] Teresa Rubio, et al. The phosphatase PRL-3 affects intestinal homeostasis by altering the crypt cell composition

[3] Magnus Aassved Hjort, et al. Phosphatase of regenerating liver-3 (PRL-3) is overexpressed in classical Hodgkin lymphoma and promotes survival and migration

[4] Tobias S Slrdahl, et al. The phosphatase of regenerating liver-3 (PRL-3) is important for IL-6-mediated survival of myeloma cells

[5] Katarzyna Guzińska-Ustymowicz, et al. PRL-3, an emerging marker of carcinogenesis, is strongly associated with poor prognosis

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Keywords: PRL-3 Inhibitor I supplier, inhibitors, activators


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