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CMPD1 

Cat. No. M30062
CMPD1  Structure
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Biological Activity

CMPD1 is a selective and non-ATP-competitive p38 MAPK-mediated MK2 phosphorylation inhibitor with apparent Ki (Kiapp) of 330 nM.

Chemical Information
Molecular Weight 349.4
Formula C22H20FNO2
CAS Number 41179-33-3
Form Solid
Solubility (25°C) DMSO 100 mg/mL (ultrasonic)
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] Prabhudutta Mamidi, et al. PLoS Pathog. MK2a inhibitor CMPD1 abrogates chikungunya virus infection by modulating actin remodeling pathway

[2] Yu Li, et al. Biol Res. CMPD1 inhibited human gastric cancer cell proliferation by inducing apoptosis and G2/M cell cycle arrest

[3] Fms Gurgis, et al. Cell Death Discov. Cytotoxic activity of the MK2 inhibitor CMPD1 in glioblastoma cells is independent of MK2

[4] Athena F Phoa, et al. Biochem Pharmacol. Pharmacology of novel small-molecule tubulin inhibitors in glioblastoma cells with enhanced EGFR signalling

[5] N Tommerup, et al. Nat Genet. Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1

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  Catalog
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Keywords: CMPD1  supplier, p38 MAPK, inhibitors, activators


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