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
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
provides coniferyl ferulate(CAS#:36417-86-4) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
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No Article Available.
Description :
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].