上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Icariside D2 纯度: ≥98.0%
Icariside D2 可从Annona glabra 中分离得到,可抑制血管紧张素转换酶。Icariside 对HL-60 细胞的IC50 值为9.0 ± 1.0 μM。Icariside D2 可诱导凋亡。

Icariside D2 Chemical Structure
CAS No. : 38954-02-8
规格 | 价格 | 是否有货 | 数量 |
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1 mg | ¥4860 | In-stock | |
5 mg | 询价 | ||
10 mg | 询价 |
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生物活性 |
Icariside D2, isolated from Annona glabra fruit, inhibits angiotensin-converting enzyme. Icariside D2 shows significant cytotoxic activity on the HL-60 cell line with the IC50 value of 9.0 ± 1.0 μM. Icariside D2 induces apoptosis [1][2]. |
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体外研究 (In Vitro) |
Icariside D2 3 induces apoptosis via alteration of expression of apoptosis-related proteins and decreases phosphorylation of AKT in HL-60 cells[1]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only. |
分子量 |
300.30 |
Formula |
C14H20O7 |
CAS 号 |
38954-02-8 |
性状 |
固体 |
颜色 |
White to off-white |
结构分类 |
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初始来源 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
储存方式 |
4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) |
纯度 & 产品资料 |
纯度: ≥98.0%
Data Sheet (526 KB) SDS (393 KB)
COA (167 KB) 产品使用指南 (1538 KB) |
参考文献 |
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