N-trans-Feruloyltyramine structure
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Common Name | N-trans-Feruloyltyramine | ||
|---|---|---|---|---|
| CAS Number | 66648-43-9 | Molecular Weight | 313.348 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 554.2±60.0 °C at 760 mmHg | |
| Molecular Formula | C18H19NO4 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 289.0±32.9 °C | |
| Symbol |
GHS09 |
Signal Word | Warning | |
Use of N-trans-FeruloyltyramineN-trans-Feruloyltyramine (N-feruloyltyramine), an alkaloid from Piper nigru, is an inhibitor of COX1 and COX2, with potential antioxidant properties. N-trans-Feruloyltyramine possesses anti-inflammatory activity[1]. |
| Name | (2E)-3-(4-Hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]ac rylamide |
|---|---|
| Synonym | More Synonyms |
| Description | N-trans-Feruloyltyramine (N-feruloyltyramine), an alkaloid from Piper nigru, is an inhibitor of COX1 and COX2, with potential antioxidant properties. N-trans-Feruloyltyramine possesses anti-inflammatory activity[1]. |
|---|---|
| Related Catalog | |
| Target |
COX-1 COX-2 |
| References |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 554.2±60.0 °C at 760 mmHg |
| Molecular Formula | C18H19NO4 |
| Molecular Weight | 313.348 |
| Flash Point | 289.0±32.9 °C |
| Exact Mass | 313.131409 |
| PSA | 78.79000 |
| LogP | 3.33 |
| Vapour Pressure | 0.0±1.6 mmHg at 25°C |
| Index of Refraction | 1.566 |
| Storage condition | ?20°C |
| Precursor 0 | |
|---|---|
| DownStream 2 | |
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Transgenic tomato plants overexpressing tyramine N-hydroxycinnamoyltransferase exhibit elevated hydroxycinnamic acid amide levels and enhanced resistance to Pseudomonas syringae.
Mol. Plant Microbe Interact. 27(10) , 1159-69, (2014) Hydroxycinnamic acid amides (HCAA) are secondary metabolites involved in plant development and defense that have been widely reported throughout the plant kingdom. These phenolics show antioxidant, an... |
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A feruloyltyramine trimer isolated from potato common scab lesions
Phytochemistry 71(17-18) , 2187-9, (2010) Graphical abstract A lignanamide isolated from potato common scab lesions was characterized as a feruloyltyramine trimer by MS and NMR techniques. |
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Endosperm-specific expression of serotonin N-hydroxycinnamoyltransferase in rice.
Plant Foods Hum. Nutr. 63(2) , 53-7, (2008) Serotonin N-hydroxycinnamoyltransferase (SHT) is a key enzyme in the synthesis of feruloylserotonin (FS) and 4-coumaroylserotonin (CS). These serotonin derivatives show strong antioxidant activity, ma... |
| 6,7-dimethoxy-5-hydroxyflavone |
| 5-Hydroxy-6,7-dimethoxy-2-phenyl-4H-chromen-4-one |
| N-trans-Feruloyltyramine |
| (1E,2E)-3-(4-Hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-2-propenimidic acid |
| 5-Hydroxy-6,7-dimethoxyflavone |
| (2E)-3-(4-Hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamide |
| 5-hydroxy-6,7-dimethoxy-2-phenyl-4H-1-benzopyran-4-one |
| 6,7-di-O-methyl-baicalein |
| moupinamide |
| 2-Propenimidic acid, 3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-, (1E,2E)- |
| 4H-1-Benzopyran-4-one,5-hydroxy-6,7-dimethoxy-2-phenyl |
| baicalein 6,7-dimethyl ether |
| 2-Propenamide, 3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-, (2E)- |
| Mosloflavone |