IGF-IA inhibitors belong to a class of compounds designed to target and modulate the activity of Insulin-Like Growth Factor-IA (IGF-IA), a critical protein involved in cell growth, proliferation, and differentiation. These inhibitors are specifically engineered to interact with IGF-IA and hinder its signaling pathways, primarily by disrupting the binding of IGF-IA to its cellular receptors, such as the IGF-1 receptor (IGF-1R) and insulin receptor (IR). By doing so, they exert a regulatory influence over the intricate network of cellular processes that IGF-IA governs.
Chemically, IGF-IA inhibitors can take on various forms, including small molecules and biologics like monoclonal antibodies. Small molecules typically interfere with IGF-IA function by directly binding to its active sites, impeding its ability to interact with its receptor molecules. Monoclonal antibodies, on the other hand, work by specifically recognizing and binding to IGF-IA or its receptors, leading to the inhibition of downstream signaling events. The development of IGF-IA inhibitors has garnered significant interest in the scientific and pharmaceutical communities due to their potential impact on various cellular and physiological processes. Researchers are also exploring their role in elucidating the intricate mechanisms governing cell growth, metabolism, and tissue development. Understanding how IGF-IA inhibitors interact with their target can provide invaluable insights into the fundamental biology of growth and may have implications in fields such as cancer research, where aberrant IGF-IA signaling is often implicated in tumorigenesis. These inhibitors serve as powerful tools for dissecting the intricate web of molecular interactions governing cellular responses to growth signals, shedding light on the underlying biology of various diseases and potentially paving the way for novel approaches in disease management.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
IGF-1R Inhibitor, PPP | 477-47-4 | sc-204008A sc-204008 sc-204008B | 1 mg 10 mg 100 mg | $112.00 $199.00 $877.00 | 63 | |
PPP is a small molecule inhibitor that blocks IGF-1R tyrosine kinase activity, inhibiting downstream signaling. | ||||||
NVP-AEW541 | 475489-16-8 | sc-507395 | 5 mg | $285.00 | ||
NVP-AEW541 is a small molecule inhibitor that disrupts IGF-1R signaling by inhibiting its tyrosine kinase activity. | ||||||
BMS-754807 | 1001350-96-4 | sc-507396 | 5 mg | $304.00 | ||
BMS-754807 is a small molecule inhibitor that targets IGF-1R and blocks its tyrosine kinase activity. | ||||||
Linsitinib | 867160-71-2 | sc-396762 sc-396762A | 5 mg 10 mg | $143.00 $260.00 | 1 | |
Linsitinib is a dual inhibitor of IGF-1R and IR, disrupting IGF-IA signaling by blocking receptor phosphorylation. | ||||||
AG 1024 | 65678-07-1 | sc-205907 | 1 mg | $105.00 | 22 | |
AG1024 selectively inhibits IGF-1R tyrosine kinase, preventing downstream signaling triggered by IGF-IA. | ||||||
PQ401 | 196868-63-0 | sc-221738 | 10 mg | $146.00 | ||
PQ401 is a pyrroloquinoline derivative that inhibits IGF-IA receptor activity, disrupting downstream signaling. | ||||||
GSK1904529A | 1089283-49-7 | sc-507398 | 10 mg | $321.00 | ||
GSK1904529A is a potent small molecule inhibitor targeting IGF-1R kinase activity, inhibiting IGF-IA signaling. | ||||||
BMS-536924 | 468740-43-4 | sc-507397 | 5 mg | $285.00 | ||
BMS-536924 is a small molecule inhibitor that disrupts IGF-IA signaling by blocking IGF-1R tyrosine kinase. | ||||||