NBL4 Inhibitors function through a vast array of biochemical mechanisms to impede the activity of the NBL4 protein. Compounds such as a potent kinase inhibitor could prevent the necessary phosphorylation events that are critical for NBL4 function, while a PI3K inhibitor would lead to the downregulation of the PI3K/AKT pathway, which is essential for a multitude of cellular functions, potentially including those governed by NBL4. The inhibition of MAPK/ERK kinase would suppress a key signaling pathway that might regulate NBL4 activity, and similarly, an mTOR inhibitor would interfere with growth and proliferation signals, possibly impacting NBL4 if it operates within this domain. Certain inhibitors specifically target the MAPK pathway by obstructing c-Raf kinase, p38 MAP kinase, or MEK1/2, leading to the potential reduction of NBL4 activity if it is integrated within these pathways.
Furthermore, inhibitors of JNK might depress stress-activated signaling cascades, and thus, the role of NBL4 within such pathways. Another potent PI3K inhibitor would block the same PI3K/AKT pathway, emphasizing the importance of this pathway's integrity for NBL4 function. Inhibitors that target cell cycle progression, such as the selective Aurora kinase inhibitor, would impede mitotic control mechanisms, and if NBL4 is implicated in such processes, its activity would be inhibited. The modulation of cytoskeletal dynamics by a ROCK inhibitor would potentially suppress NBL4 if it is associated with cellular motility and structure. Lastly, the disruption of developmental pathways by a BMP signaling inhibitor would lead to the inhibition of NBL4 activity if it is involved in such signaling events.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
A potent kinase inhibitor that prevents phosphorylation, thus potentially inhibiting the activity of NBL4 if it requires phosphorylation for its function. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
A phosphoinositide 3-kinase (PI3K) inhibitor, leading to downregulation of the PI3K/AKT pathway, potentially reducing NBL4 activity if it is AKT-dependent. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
A selective inhibitor of MAPK/ERK kinase, which could suppress ERK pathway activation and, in turn, negatively affect NBL4 if it is ERK-dependent. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
An mTOR inhibitor which could reduce cell growth and proliferation signals that may be vital for NBL4's function if it is mTOR-associated. | ||||||
GW 5074 | 220904-83-6 | sc-200639 sc-200639A | 5 mg 25 mg | $106.00 $417.00 | 10 | |
A c-Raf kinase inhibitor that could block the MAPK pathway, potentially leading to reduced activity of NBL4 if it is part of this pathway. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
A p38 MAP kinase inhibitor, which may decrease inflammatory responses and potentially inhibit NBL4 if it is involved in stress response signaling. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
An inhibitor of MEK1/2, which could prevent activation of the MAPK/ERK pathway, potentially inhibiting NBL4 if it is regulated by this pathway. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
An inhibitor of JNK, which might reduce the activity of NBL4 if it is part of stress-activated signaling. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
A PI3K inhibitor that could block the PI3K/AKT pathway, potentially leading to the inhibition of NBL4 if it is PI3K/AKT-dependent. | ||||||
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $150.00 $349.00 | 15 | |
A selective Aurora kinase inhibitor that could disrupt cell cycle progression, possibly inhibiting NBL4 if it is involved in mitotic control. | ||||||