D-JNKI-1 (AM-111) is a highly potent and cell-permeable peptide inhibitor of JNK.
|Solubility (25°C)||DMSO ≥ 90 mg/mL
Water ≥ 50 mg/mL
Powder -20°C 3 years ; 4°C 2 years
In solvent -80°C 6 months ; -20°C 1 month
|Body Surface Area (m2)||0.007||0.025||0.15||0.05||0.02||0.5|
|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.
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SR-3306 is a selective, potent, highly brain penetrant JNK inhibitor.
CC-90001 is a JNK (c-Jun N-terminal kinase) inhibitor that can be used as a Phase II clinical candidate to study idiopathic pulmonary fibrosis.
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L-JNKI-1 is a cell-permeable peptide inhibitor specific for JNK.
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