D-JNKI-1
Names
Biological Activity
[Description]:
D-JNKI-1 is a specific inhibitor of JNK, and strongly interferes with JNK activation.
[Related Catalog]:
[Target]
JNK
[In Vitro]
D-JNKI-1 (1 μM-1 mM) treatment prevents apoptosis and loss of neomycin-exposed hair cells[1].
[In Vivo]
D-JNKI-1 (10 μM) prevents nearly all hair cell death and permanent hearing loss induced by neomycin ototoxicity in the scala tympani of the guinea pig cochlea. Local delivery of D-JNKI-1 also prevents acoustic trauma-induced permanent hearing loss in a dose-dependent manner[1]. D-JNKI-1 (0.3 mg/kg, i.p.) reverses these pathological events in the brain mitochondria of the rat and almost completely abolishes cytochrome c release and PARP cleavage[2]. D-JNKI-1 (1 μg/kg, s.c.) results in a significant decrease in the disease activity index, and reduces the expression of CD4+ and CD8+ cells in mice[3].
[Animal admin]
D-JNKI-1 is dissolved in a 0.9% sodium chloride solution for subcutaneous application. Each group (the 1.0% DSS group and the 1.5% DSS group) is randomly subdivided into an intervention group (n = 15) and a control group (n = 15). The mice in the intervention group receive three subcutaneous nuchal administrations of 1 μg/kg D-JNKI-1 on days 2, 12, and 22. The mice in the control group receive physiological saline subcutaneously as a negative control at the same time points in a comparable stress situation.
[References]
[Related Small Molecules]
Pyrazolanthrone (SP600125)
|
JNK-IN-8
|
Tomatidine
|
CC-930
|
Astragaloside IV
|
AS601245
|
JNK-IN-7
|
BI 78D3
|
DB07268
|
SR-3306
|
Bentamapimod
|
CC-401
|
Ginsenoside Re
|
Isovitexin
|
Juglanin
Chemical & Physical Properties
[ Molecular Formula ]:
C164H286N66O40
[ Storage condition ]:
-20°C
Related Compounds
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