(Q27134147)

N-p-trans-Coumaroyltyramine (English)

7 October 2016

chemical formula

C₁₇H₁₇NO₃

1 reference

N-p-trans-Coumaroyltyramine (English)

7 October 2016

canonical SMILES

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

1 reference

N-p-trans-Coumaroyltyramine (English)

7 October 2016

isomeric SMILES

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

1 reference

Inhibitory effect ofTrans-N-p-coumaroyl tryamine from the twigs ofCeltis chinensis on the acetylcholinesterase

N-p-trans-Coumaroyltyramine (English)

7 October 2016

1 reference

Berberis vulgaris

1 reference

Antioxidant and cytoprotective compounds from Berberis vulgaris (barberry).

Aesculus hippocastanum

2 references

The distribution of hydroxycinnamic acid amides in flowering plants

Enriched production of N-hydroxycinnamic acid amides and biogenic amines in pepper (Capsicum annuum) flowers

Capsicum annuum

4 references

The distribution of hydroxycinnamic acid amides in flowering plants

New sesquiterpenes from Capsicum annuum

A New Lignan Amide, Grossamide, from Bell Pepper (Capsicum annuumvar.grossurri)

Enriched production of N-hydroxycinnamic acid amides and biogenic amines in pepper (Capsicum annuum) flowers

common sunflower

2 references

The distribution of hydroxycinnamic acid amides in flowering plants

Enriched production of N-hydroxycinnamic acid amides and biogenic amines in pepper (Capsicum annuum) flowers

Pyrus communis

2 references

The distribution of hydroxycinnamic acid amides in flowering plants

Enriched production of N-hydroxycinnamic acid amides and biogenic amines in pepper (Capsicum annuum) flowers

Rubus idaeus

2 references

The distribution of hydroxycinnamic acid amides in flowering plants

Enriched production of N-hydroxycinnamic acid amides and biogenic amines in pepper (Capsicum annuum) flowers

Solanum annuum

2 references

The distribution of hydroxycinnamic acid amides in flowering plants

Enriched production of N-hydroxycinnamic acid amides and biogenic amines in pepper (Capsicum annuum) flowers

tomato

2 references

The distribution of hydroxycinnamic acid amides in flowering plants

Enriched production of N-hydroxycinnamic acid amides and biogenic amines in pepper (Capsicum annuum) flowers

broad bean

6 references

The distribution of hydroxycinnamic acid amides in flowering plants

Enriched production of N-hydroxycinnamic acid amides and biogenic amines in pepper (Capsicum annuum) flowers

The identification of gibberellins in immature seeds of Vicia faba, and some chemotaxonomic considerations

UHPLC-ESI-QTOF-MS-based metabolic profiling of Vicia faba L. (Fabaceae) seeds as a key strategy for characterization in foodomics

Fast responses of metabolites in Vicia faba L. to moderate NaCl stress

Kaempferol 3-O-Galactoside, 7-O-Rhamnoside is the Major Green Fluorescing Compound in the Epidermis of Vicia faba

Annona cherimola

2 references

Amides from stems of annona cherimola

Amides from stems of annona cherimola

Aristolochia manshuriensis

1 reference

Constituents from the stems of Aristolochia manshuriensis

Artabotrys hexapetalus

2 references

New constituents from stems of Artabotrys uncinatus

New constituents from stems of Artabotrys uncinatus

Fumaria indica

2 references

Alkaloids of Fumaria indica

Alkaloids of Fumaria indica

Liriope muscari

1 reference

cis-Eudesmane sesquiterpene glycosides from Liriope muscari and Ophiopogon japonicus

Melicope hayesii

2 references

Lignans and coumarins metabolites from Melicopehayesii

Lignans and coumarins metabolites from Melicopehayesii

Ophiopogon japonicus

2 references

cis-Eudesmane sesquiterpene glycosides from Liriope muscari and Ophiopogon japonicus

cis-Eudesmane sesquiterpene glycosides from Liriope muscari and Ophiopogon japonicus

Peperomia heyneana

2 references

Bioactive lignans from Peperomia duclouxii

Bioactive lignans from Peperomia duclouxii

Piper umbellatum

2 references

Bioactive aristolactams from Piper umbellatum

Bioactive aristolactams from Piper umbellatum

Saussurea muliensis

1 reference

Oleanane-type triterpenes from the flowers and roots of Saussurea muliensis

Tribulus terrestris

4 references

Alkaloids and other constituents from Tribulus terrestris

Tribulusamide A and B, new hepatoprotective lignanamides from the fruits of Tribulus terrestris: indications of cytoprotective activity in murine hepatocyte culture

Tribulusamide A and B, new hepatoprotective lignanamides from the fruits of Tribulus terrestris: indications of cytoprotective activity in murine hepatocyte culture

Papain-like protease (PLpro) inhibitory effects of cinnamic amides from Tribulus terrestris fruits

Trema micrantha

1 reference

Vitexin, paprazine and terpenoids from Trema micrantha.

Arcangelisia gusanlung

2 references

Gusanlungionosides A-D, potential tyrosinase inhibitors from Arcangelisia gusanlung

Gusanlungionosides A-D, potential tyrosinase inhibitors from Arcangelisia gusanlung

Asimina triloba

1 reference

Additional bioactive compounds and trilobacin, a novel highly cytotoxic acetogenin, from the bark of Asimina triloba

Lycium chinense

1 reference

Neolignanamides, lignanamides, and other phenolic compounds from the root bark of Lycium chinense

Nelumbo nucifera

1 reference

Chemical constituents from Nelumbo nucifera leaves and their anti-obesity effects

Piper kadsura

2 references

Anti-inflammatory neolignans from Piper kadsura

Anti-inflammatory neolignans from Piper kadsura

Solanum melongena

2 references

Three new phenolic amides from the roots of eggplant (Solanum melongena L.).

Three New Phenolic Amides from the Roots of Eggplant (Solanum melongenaL.)

Welsh onion

1 reference

Isolation and Activity ofN-p-Coumaroyltyramine, anα-Glucosidase Inhibitor in Welsh Onion (Allium fistulosum)

Annona glabra

1 reference

Chemical Constituents fromAnnona GlabraIII

Annona montana

1 reference

Bioactive constitutents from the stems of Annona montana.

Aristolochia elegans

1 reference

The alkaloids and other constituents from the root and stem of Aristolochia elegans

Capsicum annuum var. annuum

1 reference

A New Lignan Amide, Grossamide, from Bell Pepper (Capsicum annuumvar.grossurri)

Crinum asiaticum

1 reference

Chemical constituents of Crinum asiaticum L. var. sinicum Baker and their cytotoxic activities

Datura metel

1 reference

Withanolides of Datura metel

Fibraurea tinctoria

1 reference

Anti-inflammatory activities of furanoditerpenoids and other constituents from Fibraurea tinctoria

Isolona congolana

1 reference

Constituents of Isolona maitlandii

Isolona maitlandii

1 reference

Constituents of Isolona maitlandii

Lindera glauca

1 reference

Alkaloids fromLindera Glauca

Macleaya microcarpa

1 reference

Cytotoxic dihydrobenzophenanthridine alkaloids from the roots of Macleaya microcarpa

Camonea bifida

1 reference

Phenolic compounds from Merremia umbellata subsp. orientalis and their allelopathic effects on Arabidopsis seed germination.

Mitrephora thorelii

1 reference

Lignanamides and Sesquiterpenoids from Stems ofMitrephora thorelii

Mitrephora tomentosa

1 reference

Lignanamides and Sesquiterpenoids from Stems ofMitrephora thorelii

Piper nigrum

1 reference

Alkaloids from Piper sarmentosum and Piper nigrum

Piper sanctum

1 reference

Antimycobacterial compounds from Piper sanctum

Polyalthia longifolia

1 reference

Anti-inflammatory and cytotoxic diterpenes from formosan Polyalthia longifolia var. pendula.

Polyalthia suberosa

1 reference

An azaanthracene alkaloid from Polyalthia suberosa

Solanum lasiocarpum

1 reference

Cytotoxic and novel compounds from Solanum indicum

Tetradium glabrifolium

1 reference

The heartwood constituents of Tetradium glabrifolium

Tinospora sinensis

1 reference

Constituents of Tinospora sinensis and their antileishmanial activity against Leishmania donovani

Solanum violaceum

2 references

Cytotoxic and novel compounds from Solanum indicum

Indiosides G-K: steroidal glycosides with cytotoxic and anti-inflammatory activities from Solanum violaceum

Erycibe hainanensis

1 reference

Hepatoprotective constituents from the roots and stems of Erycibe hainanesis

Persicaria orientalis

1 reference

Determination of paprazine in Polygonum orientale ofdifferent commodities by HPLC

Aristolochia littoralis

1 reference

The alkaloids and other constituents from the root and stem of Aristolochia elegans

Camonea umbellata

1 reference

Phenolic compounds from Merremia umbellata subsp. orientalis and their allelopathic effects on Arabidopsis seed germination.

Piper auritum

1 reference

Antimycobacterial compounds from Piper sanctum

Cannabis sativa

1 reference

Analysis and pharmacotoxicity of feruloyltyramine as a new constituent and p-coumaroyltyramine in Cannabis sativa L

Toddalia asiatica

1 reference

Compounds from Toddalia asiatica: Immunosuppressant Activity and Absolute Configurations

Annona muricata

1 reference

Additional bioactive acetogenins, annomutacin and (2,4-trans and cis)-10R-annonacin-A-ones, from the leaves of Annona muricata

potato

1 reference

Biochemical characterization of the suberization-associated anionic peroxidase of potato

Zanthoxylum asiaticum

1 reference

Compounds from Toddalia asiatica: Immunosuppressant Activity and Absolute Configurations

Identifiers

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+

1 reference

N-p-trans-Coumaroyltyramine (English)

7 October 2016

2 references

N-p-trans-Coumaroyltyramine (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

36417-86-4

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

(2E)-3-(4-Hydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]acrylamide (English)

7 October 2016

2 references

N-p-trans-Coumaroyltyramine (English)

7 October 2016

ChEBI ID

65665

mapping relation type

2 references

trans-N-p-coumaroyl tyramine (English)

7 October 2016

International Chemical Identifier

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+

1 reference

N-P-COUMAROYL TYRAMINE (English)

7 October 2016

2 references

SCHEMBL2512193

2 references

1 reference

1 reference

Human Metabolome Database ID

1 reference

HMDB0039521

2 references

KNApSAcK ID

C00028801

2 references

C00034085

2 references

UNII

5WQM3PJ2UK

1 reference