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SR-3306 

Cat. No. M27823
SR-3306  Structure
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Biological Activity

SR-3306 is a selective, potent, highly brain penetrant JNK inhibitor.

Chemical Information
Molecular Weight 490.56
Formula C28H26N8O
CAS Number 1128096-91-2
Form Solid
Solubility (25°C) DMSO 125 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] Maria Shvedova, et al. Front Pharmacol. c-Jun N-Terminal Kinases (JNKs) in Myocardial and Cerebral Ischemia/Reperfusion Injury

[2] Ni Sima, et al. Transl Oncol. Small Molecules Identified from a Quantitative Drυg Combinational Screen Resensitize Cisplatin's Response in Drυg-Resistant Ovarian Cancer Cells

[3] Su Gao, et al. Sci Rep. Pharmacological Inhibition of c-Jun N-terminal Kinase Reduces Food Intake and Sensitizes Leptin's Anorectic Signaling Actions

[4] Jeremy W Chambers, et al. J Biol Chem. Inhibition of JNK mitochondrial localization and signaling is protective against ischemia/reperfusion injury in rats

[5] Candice E Crocker, et al. ACS Chem Neurosci. JNK Inhibition Protects Dopamine Neurons and Provides Behavioral Improvement in a Rat 6-hydroxydopamine Model of Parkinson's Disease

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  Catalog
Abmole Inhibitor Catalog




Keywords: SR-3306  supplier, JNK, inhibitors, activators


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