| 貨號 | 規(guī)格 | 價格 | 上海 | 北京 | 武漢 | 南京 | 購買數(shù)量 |
|---|---|---|---|---|---|---|---|
S81210-2mg |
99.9% | ￥60.00 | 5 | - | - | - |
|
S81210-5mg |
99.9% | ￥90.00 | 6 | - | - | - |
|
S81210-10mg |
99.9% | ￥160.00 | 6 | - | - | - |
|
S81210-25mg |
99.9% | ￥252.00 | 6 | - | - | - |
|
S81210-50mg |
≥98% | ￥480.00 | 貨期：2-3天 | - | - | - |
|
S81210-100mg |
≥98% | ￥900.00 | 貨期：2-3天 | - | - | - |
|
S81210-200mg |
≥98% | ￥1600.00 | 貨期：2-3天 | - | - | - |
|
Salermide is an inhibitor of Sirt1 and Sirt2; can cause strong cancer-specific apoptotic cell death.
| 產(chǎn)品描述： | Salermide is an inhibitor of Sirt1 and Sirt2; can cause strong cancer-specific apoptotic cell death. | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 靶點(diǎn)： | SIRT1;SIRT2;Apoptosis;?Sirtuin | ||||||||||||||||||||
| 體內(nèi)研究： | Salermide is well tolerated by mice at concentrations up to 100 μM. Salermide's mechanism of action in vivo is specifically mediated by Sirt1. Intraperitoneal feeding of Salermide has no apparent toxicity in nude mice | ||||||||||||||||||||
| 參考文獻(xiàn)： | 1. Lara E, et al. Salermide, a Sirtuin inhibitor with a strong cancer-specific proapoptotic effect. Oncogene. 2009 Feb 12;28(6):781-91. | ||||||||||||||||||||
| 溶解性： | DMSO : ≥ 50 mg/mL (126.75 mM) | ||||||||||||||||||||
| 保存條件： | -20℃ | ||||||||||||||||||||
| 配置溶液濃度參考： |
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| 注意： | 部分產(chǎn)品我司僅能提供部分信息，我司不保證所提供信息的權(quán)威性，僅供客戶參考交流研究之用。 |
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北京