T2BP inhibitors are a class of chemical compounds that specifically target and inhibit the function of the protein known as TANK-binding protein (T2BP), which is involved in cellular signaling processes. T2BP, also referred to as TRAF2 and NCK-interacting protein, plays a key role in the regulation of various signaling pathways, particularly those related to immune responses and cell survival. This protein interacts with TRAF (TNF receptor-associated factors) proteins and other key signaling molecules, acting as a scaffold that facilitates the assembly of complexes involved in cellular responses to external stimuli, such as stress or inflammation. Inhibitors of T2BP function by interfering with these interactions, preventing T2BP from forming critical protein complexes, and thereby modulating the downstream signaling events that are typically regulated by these pathways.
The chemical structures of T2BP inhibitors can vary widely, depending on the specific binding interactions they are designed to disrupt. Some inhibitors work by directly binding to the T2BP protein, preventing its interaction with TRAF proteins or other signaling molecules. Others may affect the conformational structure of T2BP, altering its ability to serve as a scaffold for the assembly of signaling complexes. By inhibiting T2BP, these compounds interfere with key signaling cascades, such as the nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathway, which is crucial for regulating immune responses and cell survival. Research into T2BP inhibitors offers important insights into the molecular mechanisms that govern these complex signaling networks, shedding light on the regulatory role of T2BP in cellular processes such as inflammation, apoptosis, and stress response. Understanding the function and inhibition of T2BP helps to clarify how cells respond to various environmental and internal signals at the molecular level.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
Inhibits MEK, a kinase in the MAPK pathway. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
Inhibits p38 MAPK, a member of the MAPK family. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
Inhibits JNK, another kinase in the MAPK pathway. | ||||||
ERK Inhibitor II, FR180204 | 865362-74-9 | sc-203945 sc-203945A sc-203945B sc-203945C | 1 mg 5 mg 10 mg 50 mg | $108.00 $162.00 $234.00 $924.00 | 45 | |
Specific inhibitor of ERK, downstream of MEK in the MAPK pathway. | ||||||
SL-327 | 305350-87-2 | sc-200685 sc-200685A | 1 mg 10 mg | $107.00 $332.00 | 7 | |
Inhibits MEK1 and MEK2, impacting ERK activation. | ||||||
Doramapimod | 285983-48-4 | sc-300502 sc-300502A sc-300502B | 25 mg 50 mg 100 mg | $149.00 $281.00 $459.00 | 2 | |
Dual inhibitor of p38 MAPK and JNK. | ||||||
PD 184,352 | 212631-79-3 | sc-202759 sc-202759A | 1 mg 5 mg | $39.00 $255.00 | 34 | |
Inhibits MEK, thereby affecting downstream MAPK signaling. | ||||||
LY2228820 | 862507-23-1 | sc-364525 | 5 mg | $191.00 | 1 | |
Targets and inhibits p38 MAPK. | ||||||
Selumetinib | 606143-52-6 | sc-364613 sc-364613A sc-364613B sc-364613C sc-364613D | 5 mg 10 mg 100 mg 500 mg 1 g | $28.00 $80.00 $412.00 $1860.00 $2962.00 | 5 | |
Inhibits MEK1/2, impacting the MAPK pathway. | ||||||
JNK Inhibitor XVI | 1410880-22-6 | sc-364745 | 10 mg | $350.00 | 5 | |
Specifically inhibits JNK, affecting the MAPK pathway. | ||||||