| Identification | Back Directory | [Name]
N-trans-caffeoyltyramine | [CAS]
103188-48-3 | [Synonyms]
N-trans-caffeoyltyramine
N-trans-caffeoyltyramine >=85% (LC/MS-ELSD)
2-Propenamide, 3-(3,4-dihydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-, (2E)- | [Molecular Formula]
C17H17NO4 | [MDL Number]
MFCD24849356 | [MOL File]
103188-48-3.mol | [Molecular Weight]
299.32 |
| Chemical Properties | Back Directory | [Melting point ]
215-217 °C | [Boiling point ]
639.9±55.0 °C(Predicted) | [density ]
1.328±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C | [solubility ]
DMSO: Soluble | [form ]
Solid | [pka]
9.38±0.10(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
N-?trans-?caffeoyltyramine can be isolated from the seeds of Annona crassiflora Mart. | [Definition]
ChEBI: N-cis-Caffeoyltyramine is a member of catechols. | [References]
[1] OPEYEMI J OLATUNJI Yifeng Z Hongxia Chen. Neuroprotective effect of trans-N-caffeoyltyramine from Lycium chinense against H2O2 induced cytotoxicity in PC12 cells by attenuating oxidative stress.[J]. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2017: 895-902. DOI: 10.1016/j.biopha.2017.07.013
[2] JAE KWON KIM. Characterization of Phenethyl Cinnamamide Compounds from Hemp Seed and Determination of Their Melanogenesis Inhibitory Activity[J]. ACS Omega, 2021, 6 47: 31945-31954. DOI: 10.1021/acsomega.1c04727
[3] SEUNG‐HEE LEE F L Vimal Veeriah. A potent HNF4α agonist reveals that HNF4α controls genes important in inflammatory bowel disease and Paneth cells[J]. PLoS ONE, 2022. DOI: 10.1371/journal.pone.0266066 |
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