Angiomotin-L1 inhibitors are a class of chemical compounds specifically designed to target and inhibit the activity of Angiomotin-like 1, a protein encoded by the AMOTL1 gene. Angiomotin-like 1 (AMOTL1) is part of the angiomotin family of proteins, which are involved in regulating cell shape, movement, and proliferation by interacting with components of the cytoskeleton and signaling pathways. AMOTL1 is known for its role in modulating the organization of the actin cytoskeleton and maintaining cell junctions, thereby influencing processes such as cell migration, adhesion, and polarity. Through its interactions with other proteins, AMOTL1 participates in complex signaling networks that are crucial for the structural integrity and dynamic behavior of cells.
Structurally, Angiomotin-L1 inhibitors can include a diverse range of molecules, such as small molecules, peptides, or larger biomolecules that are engineered to interact specifically with key functional domains of the AMOTL1 protein. These inhibitors typically function by blocking the binding sites or disrupting the interactions between AMOTL1 and its target proteins, thereby inhibiting its role in regulating the cytoskeleton and cell junctions. By inhibiting AMOTL1, these compounds can alter the signaling pathways and structural arrangements mediated by this protein, leading to changes in cell morphology, motility, and adhesion. The study of Angiomotin-L1 inhibitors is essential for understanding the mechanisms by which AMOTL1 influences cellular architecture and dynamics. Research into these inhibitors provides valuable insights into the broader regulatory networks controlled by AMOTL1 and highlights the significance of cytoskeletal and junctional regulation in cellular processes. By exploring the effects of AMOTL1 inhibition, scientists can gain a deeper understanding of the physiological and biochemical pathways influenced by this protein, revealing its importance in maintaining the structural and functional organization of cells.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Verteporfin | 129497-78-5 | sc-475698 sc-475698A | 10 mg 100 mg | ¥3915.00 ¥30574.00 | 5 | |
维替泊芬是一种光敏剂,可通过破坏Hippo信号通路间接抑制血管动蛋白-L2。它可激活YAP/TAZ降解,影响血管动蛋白-L2在Hippo通路中的表达和功能,从而抑制其活性。 | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | ¥530.00 ¥1636.00 | 51 | |
达沙替尼是一种酪氨酸激酶抑制剂,通过靶向Src家族激酶间接抑制AMOTL(血管肌动蛋白样)。通过阻断Src的激活,达沙替尼调节下游信号通路,影响AMOTL(血管肌动蛋白样)在与Src介导的通路相关的细胞过程中的表达和功能。 | ||||||
Y-27632 dihydrochloride | 129830-38-2 | sc-216067 sc-216067A | 1 mg 5 mg | ¥1918.00 ¥4851.00 | 5 | |
Y-27632是一种选择性Rho相关蛋白激酶(ROCK)抑制剂,通过调节肌动蛋白细胞骨架动力学间接抑制AMOTL(血管运动蛋白样)。Y-27632通过靶向ROCK影响Angiomotin-L2的细胞过程,从而在肌动蛋白细胞骨架相关通路中调节Angiomotin-L2。 | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | ¥699.00 ¥1749.00 ¥3610.00 | 233 | |
雷帕霉素是一种mTOR抑制剂,通过破坏mTOR信号通路间接抑制AMOTL(血管肌动蛋白样蛋白)。它调节下游事件,影响AMOTL(血管肌动蛋白样蛋白)在mTOR介导的细胞过程中的表达和功能,从而抑制其活性。 | ||||||
PF-562271 | 717907-75-0 | sc-478488 sc-478488A sc-478488B | 5 mg 10 mg 50 mg | ¥3452.00 ¥5246.00 ¥12433.00 | 3 | |
PF-562271是一种细胞粘附激酶(FAK)抑制剂,通过破坏FAK介导的信号通路间接抑制AMOTL(血管运动素样蛋白)。这种抑制剂会影响下游事件,从而影响与FAK相关通路相关的细胞过程中AMOTL(血管运动素样蛋白)的表达和功能,从而对其进行调节。 | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | ¥282.00 ¥1320.00 ¥2358.00 | 27 | |
伊马替尼是一种酪氨酸激酶抑制剂,通过靶向特定的酪氨酸激酶间接抑制AMOTL(血管运动素样蛋白)。通过阻断这些激酶,伊马替尼调节下游信号通路,影响AMOTL(血管运动素样蛋白)的表达和功能,从而影响与这些酪氨酸激酶介导的通路相关的细胞过程。 |