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Mezigdomide (CC-92480)

Cat. No. M11295
Mezigdomide (CC-92480) Structure
Size Price Availability Quantity
5mg USD 340  USD340 In stock
10mg USD 540  USD540 In stock
50mg USD 1600  USD1600 In stock
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Quality Control & Documentation
Biological Activity

Mezigdomide (CC-92480) is a novel protein reducing agent and cereblon E3 ligase modulator (CELMoD). Mezigdomide has a strong affinity with Cereblon and has anti-myeloma activity.

Chemical Information
Molecular Weight 567.61
Formula C32H30FN5O4
CAS Number 2259648-80-9
Solubility (25°C) DMSO ≥ 40 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] Sergei G Levin, et al. Neuroreport. Interleukin-10 and PD150606 modulate expression of AMPA receptor GluA1 and GluA2 subunits under hypoxic conditions

[2] Tao Luo, et al. Arch Biochem Biophys. PD150606 protects against ischemia/reperfusion injury by preventing μ-calpain-induced mitochondrial apoptosis

[3] Zhong-Jia Ding, et al. PLoS One. Calpain inhibitor PD150606 attenuates glutamate induced spiral ganglion neuron apoptosis through apoptosis inducing factor pathway in vitro

[4] Kristin E Low, et al. Biochim Biophys Acta. Allosteric inhibitors of calpains: Reevaluating inhibition by PD150606 and LSEAL

[5] Bence Farkas, et al. Brain Res. Ischemia-induced increase in long-term potentiation is warded off by specific calpain inhibitor PD150606

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