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Phenylethyl 3,4-dihydroxycinnamate, 98+%, Thermo Scientific Chemicals
Inhibitor of protein tyrosine kinase, and is cytotoxic to cancer cell lines
$242.88 - $714.04
Chemical Identifiers
CAS | 104594-70-9 |
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Molecular Formula | C17H16O4 |
Molecular Weight (g/mol) | 284.31 |
MDL Number | MFCD00866470 |
InChI Key | SWUARLUWKZWEBQ-VQHVLOKHSA-N |
Synonym | caffeic acid phenethyl ester, phenethyl caffeate, cape, capeee, phenethyl 3-3,4-dihydroxyphenyl acrylate, phenylethyl caffeate, unii-g960r9s5sk, caffeic acid phenylethyl ester, 2-phenylethyl caffeate, caffeic acid 2-phenylethyl ester |
PubChem CID | 5281787 |
ChEBI | CHEBI:8062 |
IUPAC Name | 2-phenylethyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate |
SMILES | OC1=CC=C(\C=C\C(=O)OCCC2=CC=CC=C2)C=C1O |
Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
AAJ61386MD
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Thermo Scientific Chemicals
J61386MD |
250 mg |
Each for $242.88
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AAJ6138603
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Thermo Scientific Chemicals
J6138603 |
1 g |
Each for $714.04
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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.
ApplicationsPhenylethyl 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.
Chemical Identifiers
104594-70-9 | |
284.31 | |
SWUARLUWKZWEBQ-VQHVLOKHSA-N | |
5281787 | |
2-phenylethyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate |
C17H16O4 | |
MFCD00866470 | |
caffeic acid phenethyl ester, phenethyl caffeate, cape, capeee, phenethyl 3-3,4-dihydroxyphenyl acrylate, phenylethyl caffeate, unii-g960r9s5sk, caffeic acid phenylethyl ester, 2-phenylethyl caffeate, caffeic acid 2-phenylethyl ester | |
CHEBI:8062 | |
OC1=CC=C(\C=C\C(=O)OCCC2=CC=CC=C2)C=C1O |
Specifications
104594-70-9 | |
White to Yellow | |
MFCD00866470 | |
Light sensitive | |
Soluble in ethyl acetate at 50mg/ml; Soluble in DMSO and ethanol. | |
OC1=CC=C(\C=C\C(=O)OCCC2=CC=CC=C2)C=C1O | |
284.31 | |
CHEBI:8062 | |
≥99% | |
Phenylethyl 3,4-dihydroxycinnamate |
127°C to 129°C | |
C17H16O4 | |
250 mg | |
caffeic acid phenethyl ester, phenethyl caffeate, cape, capeee, phenethyl 3-3,4-dihydroxyphenyl acrylate, phenylethyl caffeate, unii-g960r9s5sk, caffeic acid phenylethyl ester, 2-phenylethyl caffeate, caffeic acid 2-phenylethyl ester | |
SWUARLUWKZWEBQ-VQHVLOKHSA-N | |
2-phenylethyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate | |
5281787 | |
284.31 | |
Crystalline Powder |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
RTECSNumber : UD3334375
TSCA : No
Recommended Storage : Store at -20°C
RUO – Research Use Only