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Anisomycin

An antibiotic that inhibits eukaryotic protein synthesis by inhibiting peptidyl transferase or the 80S ribosome system; sensitizes RCC cells to DR4-mediated apoptosis through the induction of DR4. (In Vitro) :To examine whether JNK has a core role in colistin-induced neurotoxicity in PC-12 cells, an SP600125 (a highly selective inhibitor of JNK) and Anisomycin (a potent activator) are used in this study. In order to select an appropriate concentration, PC-12 cells are treated with a range of SP600125 (0-80 μM) and Anisomycin (0-20 μM) respectively for 24 h. The results show that the cells viability significantly decreases by SP600125 treatment in a concentration-dependent manner, observed at the concentrations greater than 20 μM (p<0.01) . Similarly the cells viability is inhibited by Anisomycin treatment (≥8 μM) (p<0.05) . (In Vivo) :Anisomycin (60 mg/kg; for 4-week continuous intravenous administration) significantly decreases mouse body weight in a dose-related manner, compared with the control group. Anisomycin (15 mg/kg; for 4-week continuous intravenous administration) slightly and transiently decreases the mouse body weight. There is no significant difference of the mouse body weight in 5 mg/kg group.

Product Specifications

CAS Number

22862-76-6

Product Name Alternative

Flagecidin | Wuningmeisu C

Purity

>98% (HPLC)

Solubility

10 mM in DMSO

Smiles

O[C@@H]1[C@@H] (OC (C) =O) [C@@H] (CC2=CC=C (OC) C=C2) NC1

Molecular Formula

C14H19NO4

Molecular Weight

265.305

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

3,4-Pyrrolidinediol, 2-[ (4-methoxyphenyl) methyl]-, 3-acetate, (2R,3S,4S) -

Available Sizes

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