DcR2 inhibitors are a class of chemical compounds that target the Decoy Receptor 2 (DcR2), also known as TRAIL-R4, which is a member of the tumor necrosis factor receptor (TNFR) superfamily. DcR2 lacks a functional death domain, distinguishing it from other death receptors, and it acts as a decoy by binding to the ligand TNF-related apoptosis-inducing ligand (TRAIL) without triggering apoptosis. By doing so, DcR2 can modulate cell death pathways and influence cellular responses to apoptotic signals. Inhibitors of DcR2 function by interfering with its ability to bind TRAIL, thereby altering the balance between pro-apoptotic and anti-apoptotic signaling in the presence of death receptors like DR4 and DR5.
The mechanism of action for DcR2 inhibitors typically involves blocking the interaction between DcR2 and TRAIL, either by binding directly to the ligand-binding site of DcR2 or by altering the receptor's conformation, reducing its capacity to compete with death receptors for TRAIL binding. By inhibiting DcR2, these compounds help enhance the availability of TRAIL for binding to pro-apoptotic receptors, allowing the apoptotic signaling pathway to proceed more efficiently. This can lead to the selective activation of cell death processes in cells expressing functional death receptors. DcR2 inhibitors are important tools for understanding the complex regulatory mechanisms that govern apoptosis and how cells control the balance between survival and death. These inhibitors are particularly useful in research exploring the signaling dynamics within the TNFR superfamily and the role of decoy receptors in modulating apoptotic pathways.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Caspase-8 inhibitor II | 210344-98-2 | sc-3084 sc-3084A | 1 mg 3 mg | $291.00 $624.00 | 48 | |
This is a caspase-8 inhibitor that can stabilize the TRAIL-induced signaling complex, thereby potentially affecting the DcR2 mediated inhibition of apoptosis. | ||||||
Thalidomide | 50-35-1 | sc-201445 sc-201445A | 100 mg 500 mg | $111.00 $357.00 | 8 | |
As an immunomodulatory drug, Thalidomide modulates various cytokine productions, which can influence the TRAIL pathway where DcR2 is involved. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $41.00 $84.00 $275.00 | 127 | |
This is a protein synthesis inhibitor that may prevent the synthesis of DcR2, thus affecting its function in cells. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
A proteasome inhibitor that can affect NF-κB activity, potentially altering the expression of TRAIL and its receptors including DcR2. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $60.00 $265.00 $1000.00 | 163 | |
A proteasome inhibitor similar to Bortezomib that can influence NF-κB activity and thus potentially affect DcR2 pathways. | ||||||
JNK Inhibitor VIII | 894804-07-0 | sc-202673 | 5 mg | $272.00 | 2 | |
This inhibitor targets the JNK signaling pathway, which is involved in apoptosis and could intersect with DcR2 signaling pathways. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
An ERK inhibitor that can modulate the extrinsic apoptotic pathway, potentially altering the effects of DcR2. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
A PI3K inhibitor, affecting AKT signaling and potentially influencing the TRAIL pathway and DcR2's role within it. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
Similar to LY294002, Wortmannin inhibits PI3K and can indirectly affect DcR2 signaling. | ||||||