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作为OATD-02的盐酸盐形态,OATD-02 hydrochloride 是一种口服、竞争性的、可逆的及非共价结合的Arginase1和Arginase2双重抑制剂.它作为缓释抑制剂,成功阻断了细胞内精氨酸酶的活性,显示出了极低的IC50值,分别为20 nM (hARG1), 39 nM (hARG2), 39 nM (mARG1), 和 28 nM (rARG1).此外,OATD-02 hydrochloride 似乎能消除两种精氨酸酶诱导的肿瘤免疫抑制现象,并可能用于黑色素瘤的研究.
作为OATD-02的盐酸盐形态,OATD-02 hydrochloride 是一种口服、竞争性的、可逆的及非共价结合的Arginase1和Arginase2双重抑制剂.它作为缓释抑制剂,成功阻断了细胞内精氨酸酶的活性,显示出了极低的IC50值,分别为20 nM (hARG1), 39 nM (hARG2), 39 nM (mARG1), 和 28 nM (rARG1).此外,OATD-02 hydrochloride 似乎能消除两种精氨酸酶诱导的肿瘤免疫抑制现象,并可能用于黑色素瘤的研究.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | OATD-02 hydrochloride is the hydrochloride salt form of OATD-02. It is an orally effective, competitive, reversible, and non-covalent dual inhibitor of Arginase1 and Arginase2. OATD-02 hydrochloride serves as a sustained-release inhibitor that efficiently blocks the activity of intracellular arginases, with IC50 values of 20 nM (hARG1), 39 nM (hARG2), 39 nM (mARG1), and 28 nM (rARG1). It effectively eliminates tumor-induced immunosuppression caused by both types of arginases. This compound is utilized in research studies on melanoma. |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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