Items 1 to 10 of 12 total
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| 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 | |
LY294002 is a phosphoinositide 3-kinase (PI3K) inhibitor. CUEDC2 is known to interact with PI3K pathway components and the inhibition of PI3K by LY294002 can lead to a downstream reduction in the signaling cascade that CUEDC2 is a part of, thereby inhibiting CUEDC2's function in this pathway. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $64.00 $246.00 | 136 | |
U0126 is an inhibitor of mitogen-activated protein kinase (MEK), a kinase that lies upstream of the extracellular signal-regulated kinases (ERK) pathway, which CUEDC2 has been shown to modulate. Inhibition of MEK by U0126 could lead to reduced ERK pathway activity, resulting in functional inhibition of CUEDC2 due to its reliance on ERK signaling for its functions. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
SB203580 is a p38 MAP kinase inhibitor and CUEDC2 has interactions with MAP kinase signaling pathways. Inhibition of p38 MAP kinase by SB203580 will lead to decreased activation of downstream targets that CUEDC2 may act upon, thereby inhibiting the functional role of CUEDC2 in stress response and cytokine production. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
PD98059 is a selective inhibitor of MEK1, which acts upstream of ERK in the MAPK signaling pathway. CUEDC2 has been implicated in modulating the MAPK signaling pathway. By inhibiting MEK1, PD98059 can suppress the activation of ERK and thereby inhibit the functional role of CUEDC2 in this pathway. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 is an inhibitor of c-Jun N-terminal kinase (JNK), which is involved in inflammatory responses and apoptosis. CUEDC2 is known to be involved in the regulation of inflammatory pathways. By inhibiting JNK, SP600125 can suppress the downstream functions in which CUEDC2 is involved, effectively inhibiting CUEDC2's role in these processes. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
Wortmannin is a potent inhibitor of PI3K. CUEDC2 interacts with components of the PI3K pathway, and by inhibiting this kinase, Wortmannin could prevent the phosphorylation events necessary for CUEDC2 to exert its function within the PI3K pathway, leading to its functional inhibition. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Rapamycin is an mTOR inhibitor and can inhibit the mTOR pathway, which is involved in cell growth and proliferation. CUEDC2 has been reported to interact with components of the mTOR signaling pathway. Inhibition of mTOR by Rapamycin can attenuate the pathway's activity, thereby inhibiting the function of CUEDC2 linked to this pathway. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $94.00 $227.00 | 30 | |
PP2 is a selective inhibitor of Src family kinases. CUEDC2 has been implicated in Src signaling pathways, and inhibition of Src kinases by PP2 can lead to a functional inhibition of CUEDC2 by preventing its participation in Src-related signaling events. | ||||||
Gö 6983 | 133053-19-7 | sc-203432 sc-203432A sc-203432B | 1 mg 5 mg 10 mg | $105.00 $299.00 $474.00 | 15 | |
Go6983 is a pan-protein kinase C (PKC) inhibitor. Since CUEDC2 has been shown to be regulated by PKC-mediated phosphorylation, inhibition of PKC by Go6983 could lead to functional inhibition of CUEDC2 by preventing its phosphorylation and subsequent activation within signaling pathways. | ||||||
Ro 31-8220 | 138489-18-6 | sc-200619 sc-200619A | 1 mg 5 mg | $92.00 $245.00 | 17 | |
Ro-31-8220 is another potent PKC inhibitor. Inhibition of PKC by Ro-31-8220 can inhibit the functional role of CUEDC2 if CUEDC2's activity is PKC-dependent, which would prevent CUEDC2 from exerting its effects within PKC-mediated signaling pathways. | ||||||