N-p-trans-Coumaroyltyramine

Catalogue Number

AV-H06034

Analysis Method

HPLC,NMR,MS

Specification

98%

Storage

-20℃

Molecular Weight

283.33

Appearance

Powder

Botanical Source

Physalis alkekengi L. var.francheti (Mast.) Makino,

Structure Type

Phenylpropanoids

Category

Standards;Natural Pytochemical;API

SMILES

C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O

Synonyms

p-Coumaroyltyramine/2-Propenamide, 3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-, (2E)-/(2E)-3-(4-Hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamide/(2E)-3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide/N-trans-p-cumaroyltyramine/N-p-trans-Coumaroyltyramine/Paprazine

IUPAC Name

(E)-3-(4-hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide

Applications

N-p-trans-Coumaroyltyramine is a cinnamoylphenethyl amide isolated from polygonum hyrcanicum, acts as an acetylcholinesterase (AChE) inhibitor with an an IC50 of 122 μM. N-p-trans-Coumaroyltyramine exhibits anti-trypanosomal activity with an IC50 of 13.3 ?M for T. brucei rhodesiense[1][2].

Density

1.2±0.1 g/cm3

Solubility

Methanol

Flash Point

308.5±30.1 °C

Boiling Point

586.5±50.0 °C at 760 mmHg

Melting Point

InChl

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+

InChl Key

RXGUTQNKCXHALN-BJMVGYQFSA-N

WGK Germany

RID/ADR

HS Code Reference

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

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