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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