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CCT020312

Cat. No. M13716
CCT020312 Structure
Size Price Availability
5mg USD 176  USD176 4-7 Days
10mg USD 308  USD308 4-7 Days
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Quality Control & Documentation
Biological Activity

CCT020312 is a selective EIF2AK3/PERK activator. CCT020312 elicits EIF2A phosphorylation in cells.

Chemical Information
Molecular Weight 650.4
CAS Number 324759-76-4
Solubility (25°C) DMSO 90 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] Yunpeng Lei, et al. Biochem Biophys Res Commun. PERK activation by CCT020312 chemosensitizes colorectal cancer through inducing apoptosis regulated by ER stress

[2] Yu-Fan Yang, et al. J Inflamm Res. Dexmedetomidine Attenuates Ischemia/Reperfusion-Induced Myocardial Inflammation and Apoptosis Through Inhibiting Endoplasmic Reticulum Stress Signaling

[3] Bao-Ming Tang, et al. Gynecol Endocrinol. PERK activator CCT020312 prevents inflammation-mediated osteoporosis in the ovariectomized rats

[4] Jiachao Guo, et al. Cell Death Dis. PERK controls bone homeostasis through the regulation of osteoclast differentiation and function

[5] Xiaoli Li, et al. Front Pharmacol. CCT020312 Inhibits Triple-Negative Breast Cancer Through PERK Pathway-Mediated G1 Phase Cell Cycle Arrest and Apoptosis

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  Catalog
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Keywords: CCT020312 supplier, PERK, inhibitors, activators


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