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JH-XI-10-02 

Cat. No. M29357
JH-XI-10-02  Structure
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Biological Activity

JH-XI-10-02 is a PROTAC connected by ligands for Cereblon and CDK. JH-XI-10-02 is a highly potent and selective PROTAC CDK8 degrader, with an IC50 of 159 nM. JH-XI-10-02 causes proteasomal degradation, does not affect CDK8 mRNA levels. JH-XI-10-02 shows no effect on CDK19.

Chemical Information
Molecular Weight 920.14
Formula C53H69N5O9
CAS Number 2209085-22-1
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] Ingeborg Menzl, et al. Nat Commun. A kinase-independent role for CDK8 in BCR-ABL1+ leukemia

[2] John M Hatcher, et al. ACS Med Chem Lett. Development of Highly Potent and Selective Steroidal Inhibitors and Degraders of CDK8

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Keywords: JH-XI-10-02  supplier, PROTAC, inhibitors, activators


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