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Anisomycin

Cat. No. M5145

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Anisomycin Structure
Synonym:

Flagecidin;Wuningmeisu C

Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
10mM*1mL in DMSO USD 48 In stock
5mg USD 30 In stock
10mg USD 40 In stock
50mg USD 90 In stock
100mg USD 148 In stock
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Quality Control & Documentation
Biological Activity

Anisomycin is a pyrrolidine antibiotic, which inhibits protein synthesis, and also act as a JNK activator. Anisomycin (3 μM) decreases protein synthesis in MDA16 and MDA-MB-468 cells, and reduces colony formation by MDA-MB-468 cells. Anisomycin causes an increase in the number of apoptotic cells in MDA-MB-468 cultures, but not in MDA16 cultures. In U251 and U87 cells, anisomycin (0.01-8 μM) inhibits the cell growth in time- and concentration-dependent manners with the IC50 (48 h) values of 0.233 and 0.192 μmol/L, respectively. Anisomycin inhibits EAC cell proliferation in concentration-dependent manner.

Peritumoral administration of anisomycin (5 mg/kg) significantly suppresses Ehrlich ascites carcinoma (EAC) growth resulting in the survival of approximately 60% of the mice 90 days after EAC inoculation.

Chemical Information
Molecular Weight 265.3
Formula C14H19NO4
CAS Number 22862-76-6
Solubility (25°C) DMSO 40 mg/mL
Ethanol 10 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Monaghan D, et al. Biochem Biophys Res Commun. Inhibition of protein synthesis and JNK activation are not required for cell death induced by anisomycin and anisomycin analogues.

[2] You P, et al. Oncol Rep. In vitro and in vivo evaluation of anisomycin against Ehrlich ascites carcinoma.

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Keywords: Anisomycin, Flagecidin;Wuningmeisu C supplier, JNK, inhibitors, activators

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