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SPP-002 是一种硫酸酯类似物,作为Sialyltransferase (ST) 的潜在抑制剂,能够选择性抑制 N-糖链唾液酸化,其抑制效力比未修饰的亲本胆酸 (LCA) 提高至少一个数量级。通过抑制整合素/FAK/Paxillin 信号通路,SPP-002 减少肿瘤细胞的迁移和侵袭能力,适用于肿瘤转移的研究。
SPP-002 是一种硫酸酯类似物,作为Sialyltransferase (ST) 的潜在抑制剂,能够选择性抑制 N-糖链唾液酸化,其抑制效力比未修饰的亲本胆酸 (LCA) 提高至少一个数量级。通过抑制整合素/FAK/Paxillin 信号通路,SPP-002 减少肿瘤细胞的迁移和侵袭能力,适用于肿瘤转移的研究。

SPP-002 相关产品
| 产品描述 | SPP-002 is a sulfate ester analogue that acts as a potential Sialyltransferase (ST) inhibitor. It selectively inhibits N-glycan sialylation with at least an order of magnitude greater potency compared to the unmodified parent lithocholic acid (LCA). By inhibiting the integrin/FAK/paxillin signaling pathway, SPP-002 reduces tumor cell migration and invasion. It is applicable in research on tumor metastasis. |
| 分子式 | C24H41KO5S |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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