C17orf82 inhibitors span a range of classes, including PI3K inhibitors like LY294002 and Wortmannin that modulate the phosphatidylinositol signaling system, which is a critical pathway for numerous cellular functions including growth and survival. Other chemicals listed, such as PD98059 and U0126, which are MEK inhibitors, along with SB203580 and SP600125, which inhibit different MAP kinases, are chosen based on the possible interaction with the MAPK/ERK pathway, a pivotal route for cell division, differentiation, and response to external stress signals.
Inhibitors such as Rapamycin affect the mTOR pathway, which is central to cell growth and proliferation, indicating a broad approach to downregulating complex pathways where C17orf82 might be implicated. Proteasome and kinase inhibitors like Bortezomib, ZM-447439, Dasatinib, Imatinib, and Sorafenib are selected on the premise that C17orf82 could be part of or influence protein degradation, cell cycle progression, integrin signaling, and oncogenic transformation. These inhibitors act on specific enzymes and proteins, potentially altering the protein stability, signaling, and functional state of pathways with which C17orf82 may interact.
Items 1 to 10 of 11 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
A potent inhibitor of PI3K, which may downregulate pathways C17orf82 is involved in if it interacts with PI3K signaling. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
An MEK inhibitor, which could disrupt MAPK/ERK signaling potentially involving C17orf82. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
A p38 MAPK inhibitor that may alter stress response pathways that C17orf82 could be a part of. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
An inhibitor of c-Jun N-terminal kinase (JNK), modulating apoptosis or cellular differentiation pathways where C17orf82 may play a role. | ||||||
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 that could affect cell growth and proliferation, possibly interacting with C17orf82 functions. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
Another PI3K inhibitor, acting similarly to LY294002, potentially influencing C17orf82 through PI3K-related pathways. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
A proteasome inhibitor, could impact protein degradation pathways involving C17orf82. | ||||||
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $153.00 $356.00 | 15 | |
An Aurora kinase inhibitor, may disrupt cell division processes if C17orf82 is associated with mitosis. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $70.00 $145.00 | 51 | |
A Src kinase inhibitor, could affect signaling cascades that involve C17orf82 if it is part of integrin signaling. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $26.00 $119.00 $213.00 | 27 | |
Inhibits Bcr-Abl tyrosine kinase, potentially affecting C17orf82 if it interacts with this oncogenic signaling pathway. | ||||||