66648-43-9
66648-43-9
Chemical Structure
N-trans-Feruloyltyramine
Synonym(s): N-feruloyltyramine; Moupinamide
- CAS No.: 66648-43-9
- Formula:C18H19NO4
- Molecular Weight:313.35
IUPAC Name: (E)-3-(4-hydroxy-3-methoxyphenyl)-N-(4-hydroxyphenethyl)acrylamide
InChIKey: NPNNKDMSXVRADT-WEVVVXLNSA-N
SMILES: O=C(NCCC1=CC=C(O)C=C1)/C=C/C2=CC=C(O)C(OC)=C2
Biological Activity: N-trans-Feruloyltyramine (N-feruloyltyramine), an alkaloid, is a potent antioxidant. N-trans-Feruloyltyramine improves H2O2-induced intracellular ROS generation and decreases apoptosis. N-trans-Feruloyltyramine has the potential for oxidative stress-related neurodegenerative conditions and cancer research[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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N-trans-Feruloyltyramine | 99.90% | N-trans-Feruloyltyramine (N-feruloyltyramine), an alkaloid, is a potent antioxidant. N-trans-Feruloyltyramine improves H2O2-induced intracellular ROS generation and decreases apoptosis. N-trans-Feruloyltyramine has the potential for oxidative stress-related neurodegenerative conditions and cancer research. | ||||||||||||||||||||
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N-trans-Feruloyltyramine (Standard) | ≥98% | N-trans-Feruloyltyramine (Standard) is the analytical standard of N-trans-Feruloyltyramine. This product is intended for research and analytical applications. N-trans-Feruloyltyramine (N-feruloyltyramine), an alkaloid, is a potent antioxidant. N-trans-Feruloyltyramine improves H2O2-induced intracellular ROS generation and decreases apoptosis. N-trans-Feruloyltyramine has the potential for oxidative stress-related neurodegenerative conditions and cancer research. | ||||||||||||||||||||
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References
- [1]. Rungtip Soi-ampornkul, et al. N-trans-feruloyltyramine Protects Human Neuroblastoma SK-N-SH Cell Line Against H2O2-Induced Cytotoxicity. Natural Product CommunicationsVolume 17, Issue 8, August 2022.
- [2]. Xudong Gao, et al. Effects of N-trans-feruloyltyramine isolated from laba garlic on antioxidant, cytotoxic activities and H2O2-induced oxidative damage in HepG2 and L02 cells. Food Chem Toxicol. 2019 Aug:130:130-141. [Content Brief]
