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Phenylethyl 3,4-dihydroxycinnamate, 98+%, Thermo Scientific Chemicals
Catalog number: J61386.03
1 g, Each
Thermo Scientific Chemicals
Phenylethyl 3,4-dihydroxycinnamate, 98+%, Thermo Scientific Chemicals
Catalog number: J61386.03
1 g, Each
Quantity
Catalog number: J61386.03
also known as J61386-03
Price (USD)
412.00
Each
Quantity
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Description
Phenylethyl 3,4-dihydroxycinnamate is a potent and specific inhibitor of nuclear transcription factor, NF-κB, activation. It has been shown to significantly suppress the lipoxygenase pathway of arachidonic acid metabolism during inflammation. It inhibits HIV-1 integrase and also inhibits proliferation of transformed cells. It induces apoptosis in transformed fibroblasts, and interferes with EGF signal transduction affecting both protein kinase C and ornithine decarboxylase activity.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Phenylethyl 3,4-dihydroxycinnamate is a potent and specific inhibitor of nuclear transcription factor, NF-κB, activation. It has been shown to significantly suppress the lipoxygenase pathway of arachidonic acid metabolism during inflammation. It inhibits HIV-1 integrase and also inhibits proliferation of transformed cells. It induces apoptosis in transformed fibroblasts, and interferes with EGF signal transduction affecting both protein kinase C and ornithine decarboxylase activity.
Solubility
Soluble in ethyl acetate at 50mg/ml. Soluble in DMSO and ethanol.
Notes
Light sensitive. Incompatible with oxidizing agents and heat.
Phenylethyl 3,4-dihydroxycinnamate is a potent and specific inhibitor of nuclear transcription factor, NF-κB, activation. It has been shown to significantly suppress the lipoxygenase pathway of arachidonic acid metabolism during inflammation. It inhibits HIV-1 integrase and also inhibits proliferation of transformed cells. It induces apoptosis in transformed fibroblasts, and interferes with EGF signal transduction affecting both protein kinase C and ornithine decarboxylase activity.
Solubility
Soluble in ethyl acetate at 50mg/ml. Soluble in DMSO and ethanol.
Notes
Light sensitive. Incompatible with oxidizing agents and heat.
RUO – Research Use Only
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