N-trans-Feruloyltyramine | CAS:66648-43-9

N-trans-Feruloyltyramine

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Description:

N-trans-Feruloyltyramine(NTF) is a platelet aggregation inhibitor, which has hepatoprotective, and antioxidative effects, NTF is likely to inhibit COX enzymes, thereby suppressing P-selectin expression on platelets;NTF inhibits melanogenesis in a dose-dependent manner.

Targets:

NO | PGE | AP-1 | NOS | COX | TNF-α | JNK | Beta Amyloid | Caspase

In vitro:

Chem Biol Interact. 2015 Jun 25;235:56-62.

N-trans-feruloyltyramine inhibits LPS-induced NO and PGE2 production in RAW 264.7 macrophages: Involvement of AP-1 and MAP kinase signalling pathways.[Pubmed: 25843058]

Mitogen-activated protein kinase (MAPK) signalling pathway can regulate inflammatory and immune responses. N-trans-Feruloyltyramine (FLA) is an active phenylpropanoid compound. It possesses antioxidant, antimicrobial, anti-melanogenesis, and anticancer activities. However, the precise molecular mechanisms underlying FLA modulation of cytokine expression in LPS-stimulated RAW 264.7 macrophages have not been fully investigated. In this study, we examined the mechanisms underlying the immunomodulative effects of FLA isolated from Arcangelisia gusanlung.
METHODS AND RESULTS:
FLA strongly suppressed mRNA expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), but not tumor necrosis factor (TNF)-α, thereby inhibiting the production of nitric oxide (NO) and prostaglandin E2 (PGE2) in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. Furthermore, FLA also inhibited nuclear translocation of activation protein (AP)-1, and simultaneously decreased the expression and phosphorylation of the c-Jun N-terminal kinase (JNK) protein.
CONCLUSIONS:
These results suggest that the anti-inflammatory effects of FLA might be attributed to downregulation of COX-2 and iNOS via suppression of AP-1 and the JNK signalling pathway in RAW 264.7 macrophages.

Fitoterapia. 2010 Mar;81(2):124-31.

Antioxidant and enzyme inhibition activities and chemical profiles of Polygonum sachalinensis F.Schmidt ex Maxim (Polygonaceae).[Pubmed: 19698767]

Polygonum sachalinensis is a widespread invasive plant in Europe. Chemical profiles of its different organs were studied by HPLC-UV-ESI/MS.
METHODS AND RESULTS:
Seven major constituents quercetin-3-O-beta-D-galactopyranoside, quercetin-3-O-arabinopyranoside, lapathoside D, N-trans-Feruloyltyramine, lapathoside C, hydropiperoside, and vanicoside B were isolated and identified. The free radical-scavenging, alpha/beta-glucosidase, and acetylcholinesterase inhibitory activities of crude MeOH extracts and isolated compounds were studied. The structure-activity relationships were discussed. The chemical profiles revealed flavonoids and phenylpropanoids are the major compounds of all the organs of this plant. Quercetin-3-O-arabinopyranoside, lapathoside D, N-trans-Feruloyltyramine, lapathoside C and hydropiperoside were isolated from this species for the first time. In the alpha-glucosidase bioassay, quercetin-3-O-beta-D-galactopyranoside, lapathoside D and N-trans-Feruloyltyramine demonstrated stronger activities than the positive reference acarbose.
CONCLUSIONS:
The trend in scavenging power showed no relation to enzyme inhibition in the test models.

N-trans-Feruloyltyramine Description

Source:	The herbs of Cannabis sativa L.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

More...

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.

PMID: 29328914

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.

PMID: 29149595

Scientific Reports 2017 Dec 11;7(1):17332.
doi: 10.1038/s41598-017-17427-6.

PMID: 29230013

Molecules. 2017 Oct 27;22(11). pii: E1829.
doi: 10.3390/molecules22111829.

PMID: 29077044

J Cell Biochem. 2018 Feb;119(2):2231-2239.
doi: 10.1002/jcb.26385.

PMID: 28857247

Phytomedicine. 2018 Feb 1;40:37-47.
doi: 10.1016/j.phymed.2017.12.030.

PMID: 29496173

Kinase Assay:

Biol Pharm Bull. 2007 Oct;30(10):1972-4.

N-trans-feruloyltyramine as a melanin biosynthesis inhibitor.[Pubmed: 17917275]

In this study, we examined the effect of N-trans-Feruloyltyramine (FA) on melanogenesis in mouse B16 melanoma cells.
METHODS AND RESULTS:
Melanogenesis was inhibited by FA in a dose-dependent manner. FA exhibited a greater potency than kojic acid as a standard inhibitor of melanogenesis. Moreover, treatment of B16 melanoma cells with FA was found to cause marked decreases in the expression levels of tyrosinase.
CONCLUSIONS:
FA-induced downregulation of tyrosinase resulted in suppression of melanin biosynthesis in murine B16 melanoma cells.

Cell Research:

Neurosci Lett. 2012 Apr 4;513(2):229-32.

Protective role of N-trans-feruloyltyramine against β-amyloid peptide-induced neurotoxicity in rat cultured cortical neurons.[Pubmed: 22387154]

Enhanced oxidative stress and inflammation play important roles in the pathogenesis of Alzheimer's disease (AD). Amyloid β-peptide (Aβ), a major component of amyloid plaques, is considered to have a causal role in the development and progress of AD by being the initiator of a pathological cascade leading to oxidative stress. The present study investigated the effect of N-trans-Feruloyltyramine (NTF) purified from Polyalthia suberosa, an alkaloid shown to protect against oxidative stress and cell death.
METHODS AND RESULTS:
Pre-treatment of rat primary cortical cell cultures with 25-250μM NTF significantly attenuated 10μM Aβ(1-42)-induced neuronal death in a dose-dependent manner. Apoptotic cell death was demonstrated morphologically as well as by detection of the presence of activated caspase-3 and Bax, levels of which could be reduced by NTF pre-treatment. NTF also reduced production of reactive oxygen species induced by Aβ(1-42).
CONCLUSIONS:
These findings suggest that the protective effect of NTF against Aβ(1-42)-induced neuronal death might be due to its antioxidative property.

CAS No.	66648-43-9	Price	$288 / 10mg
Catalog No.	CFN97135	Purity	>=98%
Molecular Weight	313.4	Type of Compound	Phenylpropanoids
Formula	C₁₈H₁₉NO₄	Physical Description	Powder
Download	Manual COA MSDS	Similar structural	Comparison (Web)

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	3.1908 mL	15.9541 mL	31.9081 mL	63.8162 mL	79.7703 mL
5 mM	0.6382 mL	3.1908 mL	6.3816 mL	12.7632 mL	15.9541 mL
10 mM	0.3191 mL	1.5954 mL	3.1908 mL	6.3816 mL	7.977 mL
50 mM	0.0638 mL	0.3191 mL	0.6382 mL	1.2763 mL	1.5954 mL
100 mM	0.0319 mL	0.1595 mL	0.3191 mL	0.6382 mL	0.7977 mL

CFN98093	Cinnamamide	22031-64-7	147.2	C₉H₉NO
CFN99895	4-Hydroxycinnamamide	194940-15-3	163.2	C₉H₉NO₂
CFN98494	N-p-trans-Coumaroyltyramine	36417-86-4	283.3	C₁₇H₁₇NO₃
CFN99238	N-p-coumaroyl-N'-caffeoylputrescine	1138156-77-0	396.4	C₂₂H₂₄N₂O₅
CFN99248	N1,N10-Bis(p-coumaroyl)spermidine	114916-05-1	437.5	C₂₅H₃₁N₃O₄
CFN99316	3,4-Dihydroxycinnamamide	1202-41-1	179.2	C₉H₉NO₃
CFN99390	3,4-Diacetoxycinnamamide	129488-34-2	263.3	C₁₃H₁₃NO₅
CFN97041	Ferulamide	61012-31-5	193.2	C₁₀H₁₁NO₃
CFN97135	N-trans-Feruloyltyramine	66648-43-9	313.4	C₁₈H₁₉NO₄
CFN97268	N-trans-Feruloyl-3-methoxytyramine	78510-19-7	343.4	C₁₉H₂₁NO₅