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MS432 

Cat. No. M29762
MS432  Structure
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Biological Activity

MS432 is a first-in-class and highly selective PD0325901-based von Hippel-Lindau-recruiting PROTAC degrader for MEK1 and MEK2. MS432 displays good plasma exposure in mice, exhibiting DC50 values of 31 nM and 17 nM for MEK1, MEK2 in HT29 cells respectively.

Chemical Information
Molecular Weight 1076.06
Formula C50H65F3IN7O6S
CAS Number 2672512-44-4
Form Solid
Solubility (25°C) DMSO 260 mg/mL (ultrasonic)
Storage -20°C, protect from light, 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] Jing Liu, et al. J Am Chem Soc. Cancer Selective Target Degradation by Folate-Caged PROTACs

[2] Jianping Hu, et al. J Med Chem. Potent and Selective Mitogen-Activated Protein Kinase Kinase 1/2 (MEK1/2) Heterobifunctional Small-molecule Degraders

[3] Jieli Wei, et al. J Med Chem. Discovery of a First-in-Class Mitogen-Activated Protein Kinase Kinase 1/2 Degrader

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Keywords: MS432  supplier, PROTAC, inhibitors, activators


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