VEGI inhibitors are a class of chemical compounds that specifically target and inhibit the activity of Vascular Endothelial Growth Inhibitor (VEGI), a protein known to play a significant role in regulating angiogenesis, the process through which new blood vessels form from pre-existing vessels. VEGI is a member of the tumor necrosis factor (TNF) superfamily, and it primarily acts as an antagonist to angiogenesis, which is crucial for maintaining tissue homeostasis and regulating vascular networks. By inhibiting VEGI, researchers can effectively modulate the angiogenic process, making VEGI inhibitors essential tools for studying the mechanisms of vascular growth and development.
The inhibition of VEGI is particularly useful in research focused on understanding the complex interactions between pro-angiogenic and anti-angiogenic factors. VEGI inhibitors allow scientists to investigate how the suppression of VEGI influences endothelial cell behavior, such as proliferation, migration, and tube formation, which are critical steps in angiogenesis. Moreover, these inhibitors provide insights into the role of VEGI in maintaining the balance between angiogenesis and its inhibition, thereby contributing to a deeper understanding of how this balance affects tissue regeneration, wound healing, and other physiological processes. By using VEGI inhibitors, researchers can also explore the downstream signaling pathways activated or suppressed as a result of VEGI inhibition, further elucidating the molecular underpinnings of angiogenesis regulation. This makes VEGI inhibitors a valuable asset in the study of vascular biology and the broader field of cellular signaling.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
---|---|---|---|---|---|---|
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | ¥474.00 ¥812.00 ¥1399.00 ¥2685.00 ¥5867.00 ¥13922.00 | 11 | |
EGCG是茶叶中含量最高的儿茶素,具有抗氧化特性。它可能通过与多种信号分子和转录因子相互作用来调节TRAIL的表达,这些分子和转录因子与细胞存活和凋亡有关。 | ||||||
3,3′-Diindolylmethane | 1968-05-4 | sc-204624 sc-204624A sc-204624B sc-204624C sc-204624D sc-204624E | 100 mg 500 mg 5 g 10 g 50 g 1 g | ¥406.00 ¥722.00 ¥982.00 ¥4659.00 ¥7536.00 ¥734.00 | 8 | |
DIM是一种存在于十字花科蔬菜中的化合物,具有支持解毒过程的作用。它可能通过影响雌激素代谢和调节与细胞增殖和存活相关的信号通路来抑制TRAIL的表达。 | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | ¥293.00 ¥1038.00 ¥1354.00 ¥3497.00 ¥5641.00 ¥10244.00 ¥20545.00 | 46 | |
染料木素是一种在大豆产品中发现的异黄酮,人们对其在调节各种细胞过程中的作用进行了研究。它可能会通过影响与细胞生长和凋亡相关的信号通路来降低TRAIL的表达。 | ||||||
Ellagic Acid, Dihydrate | 476-66-4 | sc-202598 sc-202598A sc-202598B sc-202598C | 500 mg 5 g 25 g 100 g | ¥643.00 ¥1049.00 ¥2708.00 ¥8044.00 | 8 | |
鞣花酸存在于水果和坚果中,因其抗氧化特性而闻名。它可能会通过影响炎症和细胞防御机制来影响TRAIL的表达。 | ||||||
Silybin | 22888-70-6 | sc-202812 sc-202812A sc-202812B sc-202812C | 1 g 5 g 10 g 50 g | ¥609.00 ¥1264.00 ¥2279.00 ¥7897.00 | 6 | |
水飞蓟宾(silibinin)提取自水飞蓟,因其潜在的肝脏保护特性而备受关注。它可能通过影响与肝脏功能和细胞防御相关的信号通路来调节TRAIL的表达。 | ||||||
Apigenin | 520-36-5 | sc-3529 sc-3529A sc-3529B sc-3529C sc-3529D sc-3529E sc-3529F | 5 mg 100 mg 1 g 5 g 25 g 100 g 1 kg | ¥361.00 ¥2369.00 ¥8123.00 ¥12726.00 ¥25971.00 ¥34591.00 ¥57606.00 | 22 | |
芹菜素是一种存在于各种水果和蔬菜中的黄酮类化合物,以其抗氧化特性而闻名。它可能通过调节与细胞存活和凋亡相关的信号通路来抑制TRAIL的表达。 | ||||||
Indole-3-carbinol | 700-06-1 | sc-202662 sc-202662A sc-202662B sc-202662C sc-202662D | 1 g 5 g 100 g 250 g 1 kg | ¥429.00 ¥677.00 ¥1613.00 ¥3452.00 ¥11417.00 | 5 | |
I3C是一种存在于十字花科蔬菜中的化合物,以其在解毒过程中的作用而闻名。它可能通过影响雌激素代谢和细胞防御机制来调节TRAIL的表达。 | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | ¥1489.00 ¥12004.00 | 115 | |
蛋白酶体抑制剂硼替佐米(Bortezomib)可影响NF-kB信号传导,该信号传导通常在TWEAK-Fn14相互作用下游激活。通过抑制NF-kB激活,硼替佐米可间接抑制TWEAK信号传导。它还可用作蛋白酶体抑制剂,在多发性骨髓瘤和套细胞淋巴瘤治疗中破坏蛋白质降解。 | ||||||
BAY 11-7082 | 19542-67-7 | sc-200615B sc-200615 sc-200615A | 5 mg 10 mg 50 mg | ¥688.00 ¥936.00 ¥3937.00 | 155 | |
Bay 11-7082抑制NF-kB的激活。它可以通过降低TWEAK介导的细胞反应中经常涉及的通路活性来间接抑制TWEAK信号传导。 | ||||||
Parthenolide | 20554-84-1 | sc-3523 sc-3523A | 50 mg 250 mg | ¥891.00 ¥3385.00 | 32 | |
Parthenolide抑制NF-kB的激活,并以其抗炎特性而闻名。它对NF-kB的作用可以间接抑制TWEAK |