宝藿苷II,大花淫羊藿苷A,意卡瑞苷A
更新时间：2024-10-05 16:56:44
| 常用名 | 宝藿苷II | CAS号 | 55395-07-8 |
|---|---|---|---|
| 价格 | ￥2400.0/5mg ￥需询单/100mg | 纯度 | 98.0% |
| 备货期 | 3天 | 库存 | 900 mg |
| 产品详情（用途，包装等）
用途： IKarisoside A(Icarisoside-A) is a natural compound isolated from Epimedium koreanum (Berberidaceae); has anti-inflammatory properties.IC50 value:Target: in vitro: Ikarisoside A inhibited the expression of LPS-stimulated inducible nitric oxide synthase (iNOS) and the production of nitric oxide (NO) in LPS-stimulated RAW 264.7 cells and mouse bone marrow-derived macrophages (BMMs) in a concentration-dependent manner. In addition, Ikarisoside A reduced the release of pro-inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta). Furthermore, Ikarisoside A inhibited the activity of p38 kinase and nuclear factor-kappaB (NF-kappaB) [1]. Ikarisoside A is a potent inhibitor of osteoclastogenesis in RANKL-stimulated RAW 264.7 cells as well as in bone marrow-derived macrophages.The inhibitory effect of Ikarisoside A resulted in decrease of osteoclast-specific genes like matrix metalloproteinase 9 (MMP9), tartrate-resistant acid phosphatase (TRAP), receptor activator of NF-kappaB (RANK), and cathepsin K. Moreover, Ikarisoside A blocked the resorbing capacity of RAW 264.7 cells on calcium phosphate-coated plates. Ikarisoside A also has inhibitory effects on the RANKL-mediated activation of NF-kappaB, JNK, and Akt [2]. 物理化学性质： CAS号：55395-07-8 常用中文名：宝藿苷II 常用英文名：Baohuoside II 分子式：C26H28O10 分子量：500.495 密度：1.5±0.1 g/cm3 沸点：782.1±60.0 °C at 760 mmHg 熔点：N/A 闪点：264.7±26.4 °C 储存条件：2-8℃ |
- 上海化源生化科技有限公司
- 上海市 上海市 普陀区
- 产品名：宝藿苷II
- 价格：
- 纯度：98.0%
- 备货期：10天
- 联系人：化源网
- 上海吉至生化科技有限公司
- 上海市 上海市 奉贤区
- 产品名：宝藿苷II；大花淫羊藿苷A；意卡瑞苷A
- 价格： ￥2400.0/5mg
- 纯度：98.0%
- 备货期：1天
- 联系人：刘佳
- 上海阿拉丁生化科技股份有限公司
- 上海市 上海市 浦东新区
- 产品名：IKarisoside A
- 价格： ￥8550.9/5mg
- 纯度：99.0%
- 备货期：10天
- 联系人：阿拉丁
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参考价格：$780/5mg