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快速发货 顺丰冷链运输,1-2 天到达
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产品名称 | HIF ↓ ↑ | HIF1 ↓ ↑ | PHD1 ↓ ↑ | PHD2 ↓ ↑ | PHD3 ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
KC7F2 |
+
HIF-1α, IC50: 20 μM |
+
HIF-1α, IC50: 20 μM |
98% | ||||||||||||||||
Lificiguat | ✔ | 99%+ | |||||||||||||||||
BAY 87-2243 | ✔ | 99%+ | |||||||||||||||||
PX-478·2HCl | ✔ | 98%+ | |||||||||||||||||
2-Methoxyestradiol | ✔ | 98% | |||||||||||||||||
CAY10585 |
++
HIF, IC50: 4.4 μM |
BCRP | 97% | ||||||||||||||||
DMOG | ✔ | 98% | |||||||||||||||||
FG 2216 |
++
PHD2, IC50: 3.9 μM |
99%+ | |||||||||||||||||
MK-8617 |
++++
PHD1, IC50: 1 nM |
++++
PHD2, IC50: 1 nM |
++++
PHD3, IC50: 14 nM |
99%+ | |||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | SYP-5 acts as an inhibitor of the hypoxia-induced increase in HIF-1 levels. It effectively suppresses both HIF-1 and the subsequent gene expression in Hep3B and Bcap37 cells. SYP-5 also hinders the migration and invasion of tumor cells, along with tumor angiogenesis, by targeting the PI3K/AKT and MAPK/ERK pathways that are dependent on HIF-1. The HIF-1 target proteins, VEGF and MMP-2, are downregulated by SYP-5, which significantly curtails the hypoxia-driven overexpression of these proteins in both cell lines. In vitro, SYP-5 inhibits angiogenesis as observed in tube formation assays, induced by both hypoxia and VEGF. Moreover, SYP-5 slows down the migration and invasion of Hep3B and Bcap37 cells caused by hypoxia and FBS. Notably, SYP-5 selectively blocks the hypoxia-induced luciferase expression in U251-HRE cells but not in U251-pGL3[1]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
3.20mL 0.64mL 0.32mL |
16.01mL 3.20mL 1.60mL |
32.01mL 6.40mL 3.20mL |
CAS号 | 1384268-04-5 |
分子式 | C18H16O3S |
分子量 | 312.38 |
SMILES Code | O=C(C1=C(O)C(C=CC(C)(C)O2)=C2C=C1)/C=C/C3=CC=CS3 |
MDL No. | MFCD30534394 |
别名 | |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Keep in dark place, sealed in dry, 2-8°C |
溶解方案 |
请根据您的动物给药指南选择适当的溶解方案。 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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