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Anisomycin

SKU: orb1225596

描述

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.

图片与验证

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关键属性

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CAS 号22862-76-6
MW265.305
纯度>98% (HPLC)
分子式C14H19NO4
SMILESO[C@@H]1[C@@H](OC(C)=O)[C@@H](CC2=CC=C(OC)C=C2)NC1
靶点Antibacterial
溶解性10 mM in DMSO

生物活性

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体内
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. Animal model: Balb/c mice of both sexes (4-5 weeks old). Dosage: 84, 99, 116, 136 or 160 mg/kg; 0.2 mL per mouse. Administration: Intravenously injected through mouse tail vein. Result: The calculated LD50 for Anisomycin was 119.64 mg/kg.
体外
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).

储存与操作

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储存Storage temperature: -20°C. Stability: ≥ 2 years
有效期12 months from date of receipt.
免责声明For research use only

别名

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Flagecidin | Wuningmeisu C

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实验方案信息

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500 mg
10 mg
¥ 1,170.00
25 mg
¥ 1,560.00
50 mg
¥ 2,080.00
100 mg
¥ 3,510.00
200 mg
¥ 4,680.00