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NT219 

Cat. No. M27918
NT219  Structure
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Biological Activity

NT219 is a potent and dual inhibitor of insulin receptor substrates 1/2 (IRS1/2) and STAT3. IRS1/2 and STAT3 are major signaling junctions regulated by various oncogenes. NT219 affects IRS1/2 degradation and inhibits STAT3 phosphorylation. NT219 has the potential for the research of cancer diseases.

Chemical Information
Molecular Weight 412.26
Formula C16H14BrNO5S
CAS Number 1198078-60-2
Form Solid
Solubility (25°C) DMSO ≥ 100 mg/mL
Storage -20°C, protect from light, dry, sealed
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] Lingling E, et al. Stem Cells Dev. Effect of Insulin on Bone Formation Ability of Rat Alveolar Bone Marrow Mesenchymal Stem Cells

[2] Adi Jacob Berger, et al. Nat Cancer. IRS1 phosphorylation underlies the non-stochastic probability of cancer cells to persist during EGFR inhibition therapy

[3] Xiaolan Yang, et al. Clin Exp Rheumatol. Modulation of miR-548m encoded by X chromosome on the PTEN pathway in systemic lupus erythematosus

[4] Lorna Moll, et al. FASEB J. The inhibition of IGF-1 signaling promotes proteostasis by enhancing protein aggregation and deposition

[5] Tayir El-Ami, et al. Aging Cell. A novel inhibitor of the insulin/IGF signaling pathway protects from age-onset, neurodegeneration-linked proteotoxicity

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Keywords: NT219  supplier, Insulin Receptor, inhibitors, activators


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