ITE
10mM in DMSO
- Product Code: 199077
CAS:
448906-42-1
| Molecular Weight: | 286.31 g./mol | Molecular Formula: | C₁₄H₁₀N₂O₃S |
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| Density: | Storage Condition: | -20°C |
Product Description:
ITE is widely used in immunological research due to its ability to modulate the aryl hydrocarbon receptor (AhR), a key player in immune regulation. It has been shown to promote the differentiation of regulatory T cells (Tregs), which are essential for maintaining immune tolerance and preventing autoimmune diseases. This makes ITE a valuable tool in studies focused on autoimmune disorders, transplant rejection, and inflammatory conditions.
In cancer research, ITE demonstrates potential in suppressing excessive immune responses that can contribute to tumor progression. It is also explored for its role in enhancing the efficacy of immunotherapies by fine-tuning the tumor microenvironment.
Additionally, ITE is used in developmental biology to study AhR signaling pathways during embryogenesis and tissue development. Its stability and potency compared to endogenous AhR ligands make it a preferred choice in experimental models requiring precise control of receptor activation.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1ml | 10-20 days | $86.48 |
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ITE
ITE is widely used in immunological research due to its ability to modulate the aryl hydrocarbon receptor (AhR), a key player in immune regulation. It has been shown to promote the differentiation of regulatory T cells (Tregs), which are essential for maintaining immune tolerance and preventing autoimmune diseases. This makes ITE a valuable tool in studies focused on autoimmune disorders, transplant rejection, and inflammatory conditions.
In cancer research, ITE demonstrates potential in suppressing excessive immune responses that can contribute to tumor progression. It is also explored for its role in enhancing the efficacy of immunotherapies by fine-tuning the tumor microenvironment.
Additionally, ITE is used in developmental biology to study AhR signaling pathways during embryogenesis and tissue development. Its stability and potency compared to endogenous AhR ligands make it a preferred choice in experimental models requiring precise control of receptor activation.
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