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.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Verteporfin | 129497-78-5 | sc-475698 sc-475698A | 10 mg 100 mg | $347.00 $2710.00 | 5 | |
Verteporfin, a photosensitizer, indirectly inhibits Angiomotin-L2 by disrupting the Hippo signaling pathway. It activates YAP/TAZ degradation, impacting the expression and function of Angiomotin-L2 within the Hippo pathway and subsequently leading to its inhibition. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
Dasatinib, a tyrosine kinase inhibitor, indirectly inhibits AMOTL (angiomotin like) by targeting Src family kinases. By disrupting the activation of Src, Dasatinib modulates downstream signaling pathways, influencing AMOTL (angiomotin like) expression and function within cellular processes associated with Src-mediated pathways. | ||||||
Y-27632 dihydrochloride | 129830-38-2 | sc-216067 sc-216067A | 1 mg 5 mg | $170.00 $430.00 | 5 | |
Y-27632, a selective Rho-associated protein kinase (ROCK) inhibitor, indirectly inhibits AMOTL (angiomotin like) through the regulation of actin cytoskeleton dynamics. By targeting ROCK, Y-27632 influences cellular processes that impact Angiomotin-L2, leading to its modulation within the context of actin cytoskeleton-associated pathways. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Rapamycin, an mTOR inhibitor, indirectly inhibits AMOTL (angiomotin like) by disrupting the mTOR signaling pathway. It modulates downstream events that influence AMOTL (angiomotin like) expression and function within cellular processes associated with mTOR-mediated pathways, leading to its inhibition. | ||||||
PF-562271 | 717907-75-0 | sc-478488 sc-478488A sc-478488B | 5 mg 10 mg 50 mg | $306.00 $465.00 $1102.00 | 3 | |
PF-562271, a focal adhesion kinase (FAK) inhibitor, indirectly inhibits AMOTL (angiomotin like) by disrupting FAK-mediated signaling pathways. This inhibitor influences downstream events that impact AMOTL (angiomotin like) expression and function within cellular processes associated with FAK-related pathways, leading to its modulation. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
Imatinib, a tyrosine kinase inhibitor, indirectly inhibits AMOTL (angiomotin like) by targeting specific tyrosine kinases. By disrupting these kinases, Imatinib modulates downstream signaling pathways, influencing AMOTL (angiomotin like) expression and function within cellular processes associated with these tyrosine kinase-mediated pathways. | ||||||