Kinase inhibitors such as Staurosporine can alter the phosphorylation state of numerous proteins, which is a common regulatory mechanism for protein function. Similarly, LY294002 and Wortmannin are both PI3K inhibitors, working to alter phosphatidylinositol signaling, which is pivotal in numerous cellular functions such as growth, proliferation, and survival, and could influence the activity of proteins like C17orf59.
The inhibitors within this class encompass agents that target protein synthesis and degradation, such as rapamycin and bortezomib, respectively. Rapamycin's action on mTOR can affect the cellular economy of protein manufacture, while bortezomib's proteasome inhibition can lead to the accumulation of proteins, potentially including C17orf59, influencing their cellular concentration and function. Other inhibitors like U0126, PD98059, and SB203580 specifically target kinases within the MAPK/ERK and p38 MAPK pathways, which are integral to cellular responses to external stimuli and stress. The breadth of this chemical class extends to the regulation of cell cycle and division through ZM-447439, a specific inhibitor of Aurora kinases, and to the modulation of signal transduction via NF449, which targets G-protein signaling pathways.
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Items 1 to 10 of 12 total
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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 $153.00 $396.00 | 113 | |
A kinase inhibitor, known to inhibit a wide range of protein kinases, which may affect phosphorylation states of proteins like C17orf59. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
A PI3K inhibitor, which may alter signaling pathways involving lipid kinase signaling, possibly affecting C17orf59-related pathways. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $64.00 $246.00 | 136 | |
An inhibitor of MEK, which may disrupt MAPK/ERK signaling and therefore influence the function of C17orf59 if it is part of this pathway. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
An mTOR inhibitor, which may affect protein synthesis and autophagy pathways, potentially influencing the turnover of C17orf59. | ||||||
Cyclopamine | 4449-51-8 | sc-200929 sc-200929A | 1 mg 5 mg | $94.00 $208.00 | 19 | |
A hedgehog signaling pathway inhibitor, which may alter signaling pathways in which C17orf59 may be involved. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
Another MEK inhibitor, which may affect the MAPK/ERK pathway and alter the functional context in which C17orf59 operates. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
A p38 MAPK inhibitor, which may influence stress response pathways and potentially the activity of C17orf59. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
A JNK inhibitor, which may impact signaling pathways associated with apoptosis and thus alter C17orf59's activity if it is linked to these pathways. | ||||||
NF449 | 627034-85-9 | sc-478179 sc-478179A sc-478179B | 10 mg 25 mg 100 mg | $203.00 $469.00 $1509.00 | 1 | |
A G-protein inhibitor, which may disrupt G-protein coupled receptor signaling pathways that could involve C17orf59. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
A proteasome inhibitor, which may stabilize proteins such as C17orf59 by preventing their degradation. | ||||||