The chemical class termed IGFN1 Inhibitors represents a diverse array of compounds selected for their capacity to modulate the cellular processes and pathways in which the IGFN1 protein is implicated. This class is defined by the shared target of action rather than a common chemical structure, emphasizing the functional impact on IGFN1's involvement in cell adhesion, signal transduction, and immune system functioning. The inhibitors in this category operate through various mechanisms, each tailored to interfere with the specific interactions and functions of IGFN1. Some of these mechanisms include the disruption of protein-protein interactions, inhibition of enzymatic activities within relevant pathways, and modulation of cellular signaling cascades. By targeting these mechanisms, the inhibitors are able to exert influence over IGFN1's role, albeit indirectly, given the absence of direct interaction with the protein.
The selection of inhibitors within this class is informed by a nuanced understanding of IGFN1's functions and the cellular pathways it engages in. Recognizing the protein's involvement in cell adhesion processes, compounds that can disrupt integrin-mediated adhesion are considered viable candidates for indirect inhibition. Similarly, given IGFN1's role in cellular signaling, inhibitors that affect key signaling pathways, such as those involving GTPases, PI3K, MAPK/ERK, and others, are included. The diversity of these inhibitors, ranging from small molecule inhibitors to kinase inhibitors, reflects the complexity and multiplicity of IGFN1's roles within the cell. This diversity is essential to address the various facets of IGFN1's involvement in cellular functions effectively. The IGFN1 Inhibitors class stands as a testament to the intricate interplay between chemical entities and biological pathways.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Fibronectin | sc-29011 sc-29011A | 1 mg 5 mg | $140.00 $494.00 | 94 | ||
By disrupting integrin-mediated cell adhesion, Fibronectin Inhibitor might indirectly inhibit IGFN1's role in cell adhesion processes. | ||||||
NSC 23766 | 733767-34-5 | sc-204823 sc-204823A | 10 mg 50 mg | $148.00 $597.00 | 75 | |
NSC23766 inhibits Rac1, a GTPase involved in cell signaling. By modulating cell signaling, it could indirectly affect IGFN1's signaling functions. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
As a PI3K inhibitor, LY294002 might alter cell survival and migration pathways in which IGFN1 is involved, thereby indirectly influencing its function. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD98059 inhibits the MAPK/ERK pathway, potentially affecting IGFN1's role in cell signaling related to growth and differentiation. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
Y-27632, by inhibiting ROCK, might impact cell adhesion and motility processes where IGFN1 could be involved. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Wortmannin, another PI3K inhibitor, could indirectly affect IGFN1 by altering cell growth and apoptosis-related signaling pathways. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
As a Src kinase inhibitor, Dasatinib might disrupt cell adhesion and signaling pathways, thereby potentially impacting IGFN1's functions. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $92.00 $223.00 | 30 | |
PP2 inhibits Src kinase, potentially affecting cell migration and immune responses where IGFN1 may play a role. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580, a p38 MAPK inhibitor, might influence stress response signaling pathways potentially involving IGFN1. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125, by inhibiting JNK, could indirectly affect IGFN1's role in cell signaling under stress conditions. | ||||||