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Multi-kinase inhibitor 1 

Cat. No. M30601
Multi-kinase inhibitor 1  Structure
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Biological Activity

Multi-kinase inhibitor 1 is a potent multi-kinase inhibitor. Multi-kinase inhibitor 1 has the potential for diseases or disorders associated with abnormal or deregulated tyrosine kinase activity, particularly diseases associated with the activity of PDGF-R, c-Kit and Bcr-abl.

Chemical Information
Molecular Weight 418.37
Formula C20H17F3N4O3
CAS Number 778274-97-8
Form Solid
Solubility (25°C) DMSO 100 mg/mL (ultrasonic and warming and heat to 60°C)
Storage 4°C, protect from light
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] Yongwen Luo, et al. Int J Biol Macromol. HIF1α lactylation enhances KIAA1199 transcription to promote angiogenesis and vasculogenic mimicry in prostate cancer

[2] Chuan-Yuan Wei, et al. J Hepatol. PKCα/ZFP64/CSF1 axis resets the tumor microenvironment and fuels anti-PD1 resistance in hepatocellular carcinoma

[3] Jingwen Jiang, et al. Autophagy. Regorafenib induces lethal autophagy arrest by stabilizing PSAT1 in glioblastoma

[4] Shingo Miyamoto, et al. Jpn J Clin Oncol. Drug review: Pazopanib

[5] Masaru Katoh. Int J Mol Med. FGFR inhibitors: Effects on cancer cells, tumor microenvironment and whole-body homeostasis (Review)

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  Catalog
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