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36417-86-4

36417-86-4 structure
36417-86-4 structure
  • Name: N-p-trans-Coumaroyltyramine
  • Chemical Name: (2E)-3-(4-Hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamide
  • CAS Number: 36417-86-4
  • Molecular Formula: C17H17NO3
  • Molecular Weight: 283.322
  • Catalog: Natural product Alkaloid
  • Create Date: 2019-01-01 07:42:53
  • Modify Date: 2025-08-25 20:06:52
  • 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 µM for T. brucei rhodesiense[1][2].

Name (2E)-3-(4-Hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamide
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
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 µM for T. brucei rhodesiense[1][2].
Related Catalog
Target

IC50: 122 μM (AChE)[2]

References

[1]. Moradi-Afrapoli F, et al. Cinnamoylphenethyl amides from Polygonum hyrcanicum possess anti-trypanosomal activity. Nat Prod Commun. 2012 Jun;7(6):753-5.

[2]. Kim DK, et al. Inhibitory effect of trans-N-p-coumaroyl tryamine from the twigs of Celtis chinensis on the acetylcholinesterase. Arch Pharm Res. 2003 Sep;26(9):735-8.

Density 1.2±0.1 g/cm3
Boiling Point 586.5±50.0 °C at 760 mmHg
Molecular Formula C17H17NO3
Molecular Weight 283.322
Flash Point 308.5±30.1 °C
Exact Mass 283.120850
PSA 69.56000
LogP 2.24
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.655
Storage condition 2-8℃
Hazard Codes Xi
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