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- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
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货期:1-2天
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MedChemExpress LLC
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1933.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥685.0 |
| 规格: | 5 mg | 产品价格: | ¥1510.0 |
| 规格: | 10 mg | 产品价格: | ¥2265.0 |
| 规格: | 25 mg | 产品价格: | ¥4075.0 |
| 规格: | 50 mg | 产品价格: | ¥5908.0 |
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hVEGF-IN-1
CAS No. : 1637443-98-1
MCE 国际站:hVEGF-IN-1
产品活性:hVEGF-IN-1,一种喹唑啉衍生物,可以特异性结合内部核糖体进入位点 A (IRES-A) 中富含 G 的序列,并会使 G-四链体结构不稳定。在 SPR 实验中,hVEGF-IN-1 以 0.928 μM 的 Kd 值与 IRES-A (WT) 结合。hVEGF-IN-1 可通过降低 VEGF-A 蛋白表达来阻止肿瘤细胞迁移并抑制肿瘤生长。
研究领域:Protein Tyrosine Kinase/RTK
作用靶点:VEGFR
In Vitro: hVEGF-IN-1 (compound 1) (1 nM-100 μM; 5 min) binds to IRES-A (WT) and IRES-A mutant RNA oligomer (IRES-MU1) with Kds of 1.29 and 13.4 μM by microscale thermophoresis (MST) measurements, respectively.
hVEGF-IN-1 (0.375-3 μM; 0-24 h) reduces MDA-MB-231 cell migration approximately 25% at the concentration of 3 μM.
hVEGF-IN-1 (0.1875-3 μM; 48 h) reduces the level of VEGF-A protein in MCF-7 cells.
hVEGF-IN-1 (0.375-3 μM; 48 h) decreases the relative wound closure of migrated MCF-7 cells by ∼35% at the concentration of 3 μM.
hVEGF-IN-1 (1.25-10 μM) reduces the stability of the IRES-A G-Quadruplex in a dose-dependent manner.
In Vivo: hVEGF-IN-1 (compound 1) (7.5 mg/kg; i.p. once daily for 20 d) inhibits tumor growth in a human breast tumor xenograft.
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