tyramine (Q165930)

tyramine (English)

17 November 2016

C₈H₁₁NO

1 reference

tyramine (English)

17 November 2016

C1=CC(=CC=C1CCN)O

1 reference

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

tyramine (English)

17 November 2016

1 reference

Senegalia berlandieri

3 references

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

Toxic amines and alkaloids from Acacia berlandieri

Technical note: an improved method for extraction and quantification of toxic phenethylamines from Acacia berlandieri

Senegalia greggii

2 references

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

Senegalia roemeriana

2 references

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

Gleditsia triacanthos

1 reference

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

Prosopis glandulosa

2 references

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

Alkaloids of Prosopis nigra

Adenocarpus hispanicus

1 reference

Alkaloids of Adenocarpus hispanicus (Lam.) DC Varieties

soybean

1 reference

Tyramine reduces glycinergic transmission by inhibiting presynaptic Ca(2+) channels in the rat trigeminal subnucleus caudalis.

Aristolochia gigantea

1 reference

Aristolactams and Alkamides of Aristolochia gigantea.

Clematis parviloba

1 reference

Aporphine alkaloids from Clematis parviloba and their antifungal activity

Cytisus scoparius

1 reference

(−)-3β-13α-dihydroxylupanine from cytisus scoparius

Delphinium pentagynum

1 reference

Alkaloids from Delphinium pentagynum

Desmodium triflorum

4 references

Alkaloids of Desmodium triflorum

Desmodium alkaloids. IV. Chemical and pharmacological evaluation of D. triflorum.

β-phenethylamine and tetrahydroisoquinoline alkaloids of Desmodium cephalotes

β-Phenethylamine, tetrahydroisoquinoline and indole Alkaloids of Desmodium tiliaefolium

Erythrina crista-galli

2 references

Biosynthesis of Erythrina alkaloids in Erythrina crista-galli

Structure of erysophorine: a new quaternary alkaloid of Erythrina arborescens

Gnetum montanum

1 reference

Alkaloids from the Chinese vine Gnetum montanum

Liparia parva

1 reference

Taxonomic significance of alkaloids in the genus Liparia (Fabaceae – Liparieae)

Liparia splendens

1 reference

Taxonomic significance of alkaloids in the genus Liparia (Fabaceae – Liparieae)

Echinopsis hertrichiana

1 reference

β-Phenethylamines from the cactus genus Lobivia

Echinopsis pentlandii

1 reference

β-Phenethylamines from the cactus genus Lobivia

Lyallia kerguelensis

1 reference

Amine distribution and content in several parts of the subantarctic endemic species Lyallia kerguelensis (Hectorellaceae)

Prosopis nigra

1 reference

Alkaloids of Prosopis nigra

Romneya coulteri

1 reference

Coulteroberbinone, a quaternary isoquinoline alkaloid from Romneya coulteri

Xylopia holtzii

1 reference

Quaternary isoquinoline alkaloids from Xylopia parviflora

Arisarum vulgare

1 reference

Hydroxycinnamoyl acid amides and aromatic amines in the inflorescences of some araceae species

Bossiaea aquifolium

1 reference

A survey of alkaloids in Templetonia biloba (Benth.) Polhill (Fabaceae: Brongniartieae)

Bossiaea concinna

1 reference

A survey of alkaloids in Templetonia biloba (Benth.) Polhill (Fabaceae: Brongniartieae)

Bossiaea ensata

1 reference

A survey of alkaloids in Templetonia biloba (Benth.) Polhill (Fabaceae: Brongniartieae)

Bossiaea pulchella

1 reference

A survey of alkaloids in Templetonia biloba (Benth.) Polhill (Fabaceae: Brongniartieae)

Bossiaea rosmarinifolia

1 reference

A survey of alkaloids in Templetonia biloba (Benth.) Polhill (Fabaceae: Brongniartieae)

Bossiaea walkeri

1 reference

A survey of alkaloids in Templetonia biloba (Benth.) Polhill (Fabaceae: Brongniartieae)

Bossiaea webbii

1 reference

A survey of alkaloids in Templetonia biloba (Benth.) Polhill (Fabaceae: Brongniartieae)

Crinum firmifolium

1 reference

Alkaloids from Crinum firmifolium var. hygrophilum

Crinum macowanii

2 references

Alkaloids from Crinum macowanii

Alkaloids from Crinum macowanii

Datura inoxia

1 reference

Investigation of the Alkaloid Pattern of Datura innoxia Plants by Capillary Gas-Liquid-Chromatography-Mass Spectrometry

Enterococcus faecium

1 reference

Cell growth inhibitory compound from the culture of intestinal lactic acid bacteria

Gymnocalycium gibbosum

1 reference

Alkaloids from the genus Gymnocalycium (Cactaceae)—II

Gymnocalycium marsoneri

1 reference

Alkaloids from the genus Gymnocalycium (Cactaceae)—II

Gymnocalycium monvillei

1 reference

Alkaloids from the genus Gymnocalycium (Cactaceae)—II

Gymnocalycium oenanthemum

1 reference

Alkaloids from the genus Gymnocalycium (Cactaceae)—II

Gymnocalycium riojense

1 reference

Constituents of Gymnocalycium riojense Fric ex H.Till & W.Till (Cactaceae)

Gymnocalycium stellatum

2 references

Alkaloids from the genus Gymnocalycium (Cactaceae)—II

Constituents of Gymnocalycium riojense Fric ex H.Till & W.Till (Cactaceae)

Gymnocalycium uebelmannianum

1 reference

Alkaloids from the genus Gymnocalycium (Cactaceae)—II

Hordeum vulgare

1 reference

Separation of hordenine and N-methyl derivatives from germinating barley by liquid chromatography with dual-electrode coulometric detection

Leptasterias (Hexasterias) polaris

1 reference

Novel polyhydroxysteroidal glycoside from the starfishLeptasterias polaris acervata

Monstera deliciosa

1 reference

Hydroxycinnamoyl acid amides and aromatic amines in the inflorescences of some araceae species

Nicotiana tabacum

3 references

Tyramine accumulation in Nicotiana tabacum transformed with a chimeric tryptophan decarboxylase gene

Aliphatic and aromatic amines during development of Nicotiana tabacum

Phenylpropanoid Defences in Nicotiana tabacum Cells: Overlapping Metabolomes Indicate Common Aspects to Priming Responses Induced by Lipopolysaccharides, Chitosan and Flagellin-22

Pancratium biflorum

1 reference

Glucosyloxy alkaloids from Pancratium biflorum

Pancratium maritimum

1 reference

New Alkaloids from Pancratium maritimum L

Pearsonia cajanifolia

1 reference

Alkaloidal variation in the genus Pearsonia

Pearsonia obovata

1 reference

Alkaloidal variation in the genus Pearsonia

Periplaneta americana

1 reference

High-performance liquid chromatography of biogenic amines in the corpus cardiacum of the American cockroach, Periplaneta americana

Philodendron melanochrysum

1 reference

Hydroxycinnamoyl acid amides and aromatic amines in the inflorescences of some araceae species

Philodendron erubescens

1 reference

Hydroxycinnamoyl acid amides and aromatic amines in the inflorescences of some araceae species

Philodendron glaziovii

1 reference

Hydroxycinnamoyl acid amides and aromatic amines in the inflorescences of some araceae species

Philodendron martianum

1 reference

Hydroxycinnamoyl acid amides and aromatic amines in the inflorescences of some araceae species

Philodendron tripartitum

1 reference

Hydroxycinnamoyl acid amides and aromatic amines in the inflorescences of some araceae species

Phoebe chekiangensis

1 reference

D4 dopamine receptor-selective compounds from the Chinese plant Phoebe chekiangensis

Prosopis argentina

1 reference

Biologically active alkaloids and a free radical scavenger from Prosopis species

Remusatia vivipara

1 reference

Hydroxycinnamoyl acid amides and aromatic amines in the inflorescences of some araceae species

Stichodactyla gigantea

1 reference

Characterization of compounds that induce symbiosis between sea anemone and anemone fish

Turbinicarpus lophophoroides

1 reference

Turbinicarpus pseudomacrochele

1 reference

Turbinicarpus pseudopectinatus

1 reference

Turbinicarpus schmiedickeanus

1 reference

Zantedeschia aethiopica

1 reference

Hydroxycinnamoyl acid amides and aromatic amines in the inflorescences of some araceae species

Escherichia coli

1 reference

A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.

Capsella bursa-pastoris

1 reference

Beiträge zur Kenntnis der wirksamen Bestandteile des Hirtentäschelkrautes (Herba Capsellae Bursae Pastoris)

Citrus reshni

1 reference

Biosynthesis of synephrine in citrus

Coprinopsis atramentaria

1 reference

[The basic ingredients of fungi. 10. Imidazole derivatives in the agaric Coprinus atramentarius Bull]

Galanthus trojanus

1 reference

Antiprotozoal alkaloids from Galanthus trojanus

Solanum campaniforme

1 reference

Antiophidic solanidane steroidal alkaloids from Solanum campaniforme

Homo sapiens

2 references

Recon 2.2: from reconstruction to model of human metabolism

A community-driven global reconstruction of human metabolism.

Gymnocalycium chubutense

1 reference

Alkaloids from the genus Gymnocalycium (Cactaceae)—II

Prosopis alba

1 reference

Alkaloids of Prosopis nigra

Caulophyllum thalictroides

1 reference

Analytical methods for determination of magnoflorine and saponins from roots of Caulophyllum thalictroides (L.) Michx. using UPLC, HPLC and HPTLC.

Antirrhinum majus

1 reference

The occurrence of amino acids in the aerial parts of Antirrhinum majus

Pereskia aculeata

1 reference

Pereskia aculeata: A plant food with antinociceptive activity.

Delphinium caeruleum

1 reference

Alkaloids from Delphinium pentagynum

Lolium multiflorum

1 reference

Diferulic acid as a component of cell walls of Lolium multiflorum

Magnolia obovata

1 reference

Effect of Chemical Profiling Change of Processed Magnolia officinalis on the Pharmacokinetic Profiling of Honokiol and Magnolol in Rats

Hypecoum lactiflorum

1 reference

Alkaloids from Mongolian species Hypecoum lactiflorum Kar. et Kir. Pazij.

Mahonia bealei

1 reference

A series of strategies for solving the shortage of reference standards for multi-components determination of traditional Chinese medicine, Mahoniae Caulis as a case

house mouse

1 reference

Correction for Long et al., "Insulin Receptor Substrates Irs1 and Irs2 Coordinate Skeletal Muscle Growth and Metabolism via the Akt and AMPK Pathways".

Coptis japonica

1 reference

Molecular cloning and characterization of CYP80G2, a cytochrome P450 that catalyzes an intramolecular C-C phenol coupling of (S)-reticuline in magnoflorine biosynthesis, from cultured Coptis japonica cells.

Mahonia aquifolium

1 reference

A series of strategies for solving the shortage of reference standards for multi-components determination of traditional Chinese medicine, Mahoniae Caulis as a case

Magnolia officinalis

1 reference

Effect of Chemical Profiling Change of Processed Magnolia officinalis on the Pharmacokinetic Profiling of Honokiol and Magnolol in Rats

Echinopsis mamillosa

1 reference

β-Phenethylamines from the cactus genus Lobivia

Cannabis sativa

1 reference

Constituents of Cannabis sativa L. XVII. A review of the natural constituents

Acacia angustissima

1 reference

Citrus medica

2 references

High-performance liquid chromatography methods for the analysis of adrenergic amines and flavanones in Citrus aurantium L. var. amara

Tyramine Pathways in Citrus Plant Defense: Glycoconjugates of Tyramine and Its N-Methylated Derivatives.

mandarin orange

2 references

High-performance liquid chromatography methods for the analysis of adrenergic amines and flavanones in Citrus aurantium L. var. amara

Tyramine Pathways in Citrus Plant Defense: Glycoconjugates of Tyramine and Its N-Methylated Derivatives.

Ganoderma lucidum subsp. lucidum

1 reference

Ganoderma species discrimination by dual-mode chromatographic fingerprinting: a study on stationary phase effects in hydrophilic interaction chromatography and reduction of sample misclassification rate by additional use of reversed-phase chromatogr

Ganoderma lucidum var. lucidum

1 reference

Ganoderma species discrimination by dual-mode chromatographic fingerprinting: a study on stationary phase effects in hydrophilic interaction chromatography and reduction of sample misclassification rate by additional use of reversed-phase chromatogr

1 reference

1 reference

Alkaloids Derived from Proline

Ototropis elegans

1 reference

β-Phenethylamine, tetrahydroisoquinoline and indole Alkaloids of Desmodium tiliaefolium

Caenorhabditis elegans

2 references

Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism

Metabotyping of the C. elegans sir-2.1 mutant using in vivo labeling and (13)C-heteronuclear multidimensional NMR metabolomics

common sunflower

1 reference

Metabolic profiles of sunflower genotypes with contrasting response to Sclerotinia sclerotiorum infection

Oryza sativa

1 reference

Simultaneous determination of the main metabolites in rice leaves using capillary electrophoresis mass spectrometry and capillary electrophoresis diode array detection

Capsicum annuum

1 reference

HPLC analysis of serotonin, tryptamine, tyramine, and the hydroxycinnamic acid amides of serotonin and tyramine in food vegetables

Brassica

1 reference

HPLC analysis of serotonin, tryptamine, tyramine, and the hydroxycinnamic acid amides of serotonin and tyramine in food vegetables

Acaciella angustissima

1 reference

Gymnocalycium bodenbenderianum

1 reference

Constituents of Gymnocalycium riojense Fric ex H.Till & W.Till (Cactaceae)

Cereus repandus

1 reference

Alkaloids Derived from Proline

Citrus × deliciosa

2 references

Tyramine Pathways in Citrus Plant Defense: Glycoconjugates of Tyramine and Its N-Methylated Derivatives.

High-performance liquid chromatography methods for the analysis of adrenergic amines and flavanones in Citrus aurantium L. var. amara

Grona adscendens

2 references

Some secondary plant metabolites in Desmodium adscendens and their effects on arachidonic acid metabolism

An extract ofDesmodium adscendens activates cyclooxygenase and increases prostaglandin synthesis by ram seminal vesicle microsomes

Vachellia rigidula

1 reference

Sunhangia elegans

1 reference

β-Phenethylamine, tetrahydroisoquinoline and indole Alkaloids of Desmodium tiliaefolium

Ctenodiscus crispatus

2 references

Novel polyhydroxysteroidal glycoside from the starfishLeptasterias polaris acervata

Polyhydroxysteroids from the Far-Eastern starfishCtenodiscus crispatus

Gymnocalycium quehlianum

2 references

Alkaloids from the genus Gymnocalycium (Cactaceae)—II

Constituents of Gymnocalycium riojense Fric ex H.Till & W.Till (Cactaceae)

Solanum

1 reference

HPLC analysis of serotonin, tryptamine, tyramine, and the hydroxycinnamic acid amides of serotonin and tyramine in food vegetables

Vitis vinifera

1 reference

Changes in Biogenic Amine Content of Tokaj Grapes, Wines, and Aszu-wines

Piper nigrum

2 references

New amide alkaloids from the roots of Piper nigrum

Nigramides A-S, dimeric amide alkaloids from the roots of Piper nigrum

Thalictrum flavum

1 reference

Structural and Functional Studies of Pavine N-Methyltransferase from Thalictrum flavum Reveal Novel Insights into Substrate Recognition and Catalytic Mechanism

physically interacts with

Trace amine-associated receptor 1

subject has role

agonist

1 reference

Trace amine associated receptor 1

17 August 2016

subject has role

agonist

1 reference

17 August 2016

1 reference

Medical Subject Headings

MeSH descriptor ID

D014439

adrenergic uptake inhibitors

15 March 2018

1 reference

https://plantreactome.gramene.org/PathwayBrowser/#/R-OSA-2744345&DTAB=MT

Medical Subject Headings

15 March 2018

1 reference

0 references

0 references

0 references

0 references

Tyramine

0 references

Identifiers

InChI

InChI=1S/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H2

1 reference

tyramine (English)

17 November 2016

2 references

tyramine (English)

17 November 2016

ChEBI release 2020-09-01

CAS Registry Number

51-67-2

1 reference

tyramine (English)

17 November 2016

1 reference

Tyramine (English)

17 November 2016

2 references

tyramine (English)

17 November 2016

Reaxys registry number

1099914

1 reference

tyramine (English)

19 October 2016

82946

0 references

ChEBI ID

15760

mapping relation type

2 references

TYRAMINE (English)

17 November 2016

International Chemical Identifier

InChI

InChI=1S/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H2

1 reference

TYRAMINE (English)

17 November 2016

2 references

inferred from InChIKey

MSBNK-Athens_Univ-AU510501

1 reference

MassBank accession ID

0 references

MSBNK-Athens_Univ-AU510502

0 references

MSBNK-Athens_Univ-AU510503

0 references

MSBNK-Athens_Univ-AU510507

0 references

MSBNK-Athens_Univ-AU510508

0 references

MSBNK-Athens_Univ-AU510509

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP002813

0 references

MSBNK-Keio_Univ-KO004082

0 references

MSBNK-Keio_Univ-KO004083

0 references

MSBNK-Keio_Univ-KO004084

0 references

MSBNK-Keio_Univ-KO004085

0 references

MSBNK-Keio_Univ-KO004086

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000015

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000016

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000017

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000018

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000019

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

MSBNK-Osaka_Univ-OUF00480

0 references

MSBNK-RIKEN-PR010240

0 references

MSBNK-RIKEN-PR100210

0 references

MSBNK-Univ_Connecticut-CO000231

0 references

MSBNK-Univ_Connecticut-CO000232

0 references

MSBNK-Univ_Connecticut-CO000233

0 references

MSBNK-Univ_Connecticut-CO000234

0 references

MSBNK-Univ_Connecticut-CO000235

0 references

MSBNK-GL_Sciences_Inc-GLS00100

0 references

MSBNK-IPB_Halle-PB000473

0 references

MSBNK-IPB_Halle-PB000474

0 references

MSBNK-IPB_Halle-PB000475

0 references

MSBNK-IPB_Halle-PB000476

0 references

MSBNK-IPB_Halle-PB000477

0 references

MSBNK-IPB_Halle-PB006085

0 references

MSBNK-IPB_Halle-PB006101

0 references

MSBNK-IPB_Halle-PB006102

0 references

MSBNK-Kazusa-KZ000078

0 references

SPLASH

splash10-00di-0900000000-58e8539844dcdbc977cc

0 references

splash10-00di-0900000000-e98b6b992e1a01839bb3

0 references

splash10-001i-9200000000-50c21473a7d48011358c

0 references

splash10-00di-1900000000-9b1000a8978b57919c35

0 references

splash10-00dr-0900000000-bfcd519d8cca540e68d4

0 references

splash10-00di-1900000000-443d60e576da797a70d1

0 references

splash10-0ffx-9500000000-55fc23fe7afe748d1bf1

0 references

splash10-004i-9100000000-1cccef72bfa4b910f413

0 references

splash10-0fb9-9000000000-f3e7f124fef2633f8197

0 references

splash10-00di-0900000000-65d023da9eb1b11298f7

0 references

splash10-00di-0900000000-7bf85350315173cf834d

0 references

splash10-00di-0900000000-6fee17263658cb5b3fe2

0 references

splash10-00di-2900000000-273503edc6a220e152b6

0 references

splash10-00di-0900000000-51c6cc08017f1672b791

0 references

splash10-00di-1900000000-55c25dd64462c06c5316

0 references

splash10-0f96-9500000000-5aeadc73c34cf8e33d2c

0 references

splash10-004i-9100000000-5f044e831c0d2db255fa

0 references

splash10-004i-9000000000-29bd478cd5164a0ab18e

0 references

splash10-00di-1900000000-ba59a2d5cb4492894c7d

0 references

splash10-00di-0900000000-92a1f106f25f5368d51f

0 references

splash10-00di-0900000000-65eeb2d3f37cd316a8c0

0 references

splash10-00di-0900000000-9e5f9483a94586df5ca2

0 references

splash10-000i-0900000000-0f7f05853a880bbf8c89

0 references

splash10-000i-0900000000-d7e9a8705227b4504c5c

0 references

splash10-0006-9000000000-3f02b334907c40a8315c

0 references

splash10-00di-0900000000-e98b3afc6fad78d45d38

0 references

splash10-001i-0900000000-54239e66d89de3096ca8

0 references

splash10-0079-0902000000-f09759fc06ef461f3aa5

0 references

splash10-0006-9000000000-9ffe6ee0ce68182216f7

0 references

splash10-00di-0900000000-020a5decfb44fc4f97df

0 references

splash10-004i-0930000000-d08de99a1ece2ad8acb6

0 references

splash10-00di-2900000000-80980d19fa83d4b86f91

0 references

splash10-00di-9700000000-78d2ae48da1eee18358e

0 references

splash10-00di-4900000000-8944003750ac547c2024

0 references

splash10-00di-0900000000-1fa26b2fc3ba88caef19

0 references

splash10-0fkc-7900000000-c3f8ea5dfbd1b3953450

0 references

splash10-004i-9100000000-7746910836d04eaa190b

0 references

splash10-004i-9000000000-5c0325e7114236e731a5

0 references

splash10-00or-9000000000-3091e50de2c30252fac4

0 references

splash10-00di-0900000000-13a399246897d165177e

0 references

splash10-000i-0900000000-066947a256844eb6cbdc

0 references

splash10-00di-0900000000-720deebe65e201678f14

0 references

splash10-00di-0900000000-abbff267d27434c1d73d

0 references

splash10-00fr-6900000000-73d85cc9555cda958d5c

0 references

splash10-004i-9200000000-602b74125d62222e7070

0 references

splash10-004i-9000000000-5d499cae1b7164e27b52

0 references

splash10-004i-9000000000-1134ab53467f3ae25d9e

0 references

splash10-00di-2900000000-69892c95ab2778a208b3

0 references

splash10-00di-5900000000-06818de674d807a2b632

0 references

splash10-0uvo-9900000000-130b6ae804451c70f74f

0 references

splash10-004l-9300000000-e2fc12d41e4c40a9a296

0 references

splash10-00di-0900000000-3229081a448a277191a2

0 references

splash10-004i-9000000000-92f0b12d0a64443cede8

0 references

splash10-053r-9500000000-6deb2b5d214f768ca448

0 references

NMRShiftDB structure ID

20032299

1 reference

HSDB ID

2132

1 reference

Hazardous Substances Data Bank

28 October 2019

TYRAMINE (English)

10 May 2021

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

1 reference

tyramine (English)

ECHA Substance Infocard ID

17 November 2016

100.000.106

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.000.106

27 December 2018

4-(2-aminoethyl)phenol (English)

quotation

CAS no.: 51-67-2 (English)

FL number

11.007

1 reference

quotation

CAS no.: 51-67-2 (English)

23 January 2021

11.007

1 reference

1 reference

tyramine (English)

17 November 2016

1 reference

5 February 2021

Tyramine

0 references

0 references

1 reference

tyramine (English)

17 November 2016

1 reference

Human Metabolome Database ID

HMDB0000306

2 references

based on heuristic

inferred from InChIKey

3 references

tyramine (English)

19 October 2016

inferred from InChIKey

2 references

tyramine (English)

17 November 2016

NDF-RT ID

N0000148848

1 reference

imported from Wikimedia project

tyramine (English)

17 November 2016

0 references

1 reference

1 reference

0 references

0 references

Encyclopædia Britannica Online ID

science/tyramine

subject named as

tyramine

0 references

1 reference

28 October 2013

Gran Enciclopèdia Catalana ID

tiramina

0 references

Gran Enciclopèdia Catalana ID (former scheme)

0146495

0 references

Interlingual Index ID

i116454

0 references

JECFA number

1590

1 reference

Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA)

https://docs.openalex.org/download-snapshot/snapshot-data-format

13 May 2021

Microsoft Academic ID

0 references

0 references

1 reference

26 January 2022

1 reference

5FF9 (English)

19 October 2016

1 reference

3BRA (English)

19 October 2016

1 reference

imported from Wikimedia project

4N7C (English)

19 October 2016

1 reference

1 reference

German Wikipedia

Store norske leksikon ID

0 references

1 reference

inferred by common MeSH mappings on source and on Wikidata

tyramine (English)

17 November 2016

1 reference

UMLS 2023