Anisomycin


CAS No. : 22862-76-6

(Synonyms: Flagecidin; Wuningmeisu C)

22862-76-6
Price and Availability of CAS No. : 22862-76-6
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10mg $66 In-stock
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100mg $198 In-stock
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Cat. No. : HY-18982
M.Wt: 265.31
Formula: C14H19NO4
Purity: >98 %
Solubility: DMSO : ≥ 50 mg/mL;H2O : 4 mg/mL (ultrasonic;warming;heat to 60°C)
Introduction of 22862-76-6 :

Anisomycin is a potent protein synthesis inhibitor which interferes with protein and DNA synthesis by inhibiting peptidyl transferase or the 80S ribosome system[1]. Anisomycin is a JNK activator, which increases phospho-JNK[2][3]. Anisomycin is a bacterial antibiotic[4]. IC50 & Target: DNA synthesis[1] 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) [1]. 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[3].

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