ChemicalBook--->CAS DataBase List--->36417-86-4

36417-86-4

36417-86-4 Structure

36417-86-4 Structure
IdentificationBack Directory
[Name]

N-p-trans-Coumaroyltyramine
[CAS]

36417-86-4
[Synonyms]

N-p-CouMaroyltyraMine
N-p-trans-Coumaroyltyramine
(2E)-3-(4-Hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamide
2-Propenamide, 3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-, (2E)-
[Molecular Formula]

C17H17NO3
[MOL File]

36417-86-4.mol
[Molecular Weight]

283.32
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[color ]

White to light yellow
[Major Application]

food and beverages
[InChI]

InChI=1S/C17H17NO3/c19-15-6-1-13(2-7-15)5-10-17(21)18-12-11-14-3-8-16(20)9-4-14/h1-10,19-20H,11-12H2,(H,18,21)/b10-5+
[InChIKey]

RXGUTQNKCXHALN-BJMVGYQFSA-N
[SMILES]

C(NCCC1=CC=C(O)C=C1)(=O)/C=C/C1=CC=C(O)C=C1
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

Soluble in methanol, ethanol, DMSO and other organic solvents, derived from the Solanaceae plant Solanum torvum.
[Uses]

food and beverages
[Definition]

ChEBI: Trans-N-p-coumaroyl tyramine is a hydroxycinnamic acid. It has a role as a metabolite.
[Biological Activity]

Np-trans-Coumaroyltyramine, a cinnamoylphenethyl amide isolated from Polygonum, acts as an acetylcholinesterase (AChE) inhibitor with IC50 of 122 μM. Np-trans-Coumaroyltyramine has anti-trypanosome activity with IC50 of 13.3 μM against T. brucei rhodesiense.
[target]

IC50: 122 μM (AChE)

Spectrum DetailBack Directory
[Spectrum Detail]

N-p-trans-Coumaroyltyramine(36417-86-4)1HNMR
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