(Q170545)

Gene Ontology release 2019-11-16

has use

medication

1 reference

L-Phenylalanine (English)

DrugBank

17 November 2015

L-Phenylalanin - L-Phenylalanine.svg
232 × 128; 8 KB

0 references

mass

165.079 dalton

1 reference

L-phenylalanine zwitterion

L-phenylalanine (English)

19 October 2016

1 reference

1 reference

based on heuristic

inferred from InChI

(2S)-2-Amino-3-phenylpropanoic acid

1 reference

based on heuristic

inferred from InChI

tautomer of

L-phenylalanine zwitterion

1 reference

ChEBI release 2021-03-01

chemical formula

C₉H₁₁NO₂

1 reference

L-phenylalanine (English)

19 October 2016

canonical SMILES

C1=CC=C(C=C1)CC(C(=O)O)N

1 reference

L-phenylalanine (English)

19 October 2016

isomeric SMILES

N[C@@H](CC1=CC=CC=C1)C(O)=O

1 reference

imported from Wikimedia project

14 February 2018

1.29 gram per cubic centimetre

temperature

20 degree Celsius

phase of matter

solid

1 reference

Russian Wikipedia

melting point

283 degree Celsius

1 reference

imported from Wikimedia project

Russian Wikipedia

pKa

9.24

1 reference

CRC Handbook of Chemistry and Physics (1st student edition)

safety classification and labelling

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response

2

1

0

no value

1 reference

imported from Wikimedia project

English Wikipedia

World Health Organisation international non-proprietary name

phenylalanine (English)

1 reference

Recon 2.2: from reconstruction to model of human metabolism

L-Phenylalanine (English)

19 January 2016

2 references

A community-driven global reconstruction of human metabolism.

Arabidopsis thaliana

3 references

Cytochrome P450 CYP79A2 from Arabidopsis thaliana L. Catalyzes the conversion of L-phenylalanine to phenylacetaldoxime in the biosynthesis of benzylglucosinolate

Metabolome analysis of biosynthetic mutants reveals a diversity of metabolic changes and allows identification of a large number of new compounds in Arabidopsis

AtMetExpress development: a phytochemical atlas of Arabidopsis development

Catharanthus roseus

1 reference

Biosynthesis of salicylic acid in fungus elicited Catharanthus roseus cells

Sinocrassula indica

1 reference

Bioactive constituents from chinese natural medicines. XXIV. Hypoglycemic effects of Sinocrassula indica in sugar-loaded rats and genetically diabetic KK-A(y) mice and structures of new acylated flavonol glycosides, sinocrassosides A(1), A(2), B(1),

Taraxacum formosanum

1 reference

Chemical constituents of Taraxacum formosanum

Sea lettuce

1 reference

4-Hydroxybenzoic acid: a likely precursor of 2,4,6-tribromophenol in Ulva lactuca

Atractylodes japonica

2 references

Glycosides of Atractylodes japonica.

Glycosides of Atractylodes ovata

Cajanus cajan

1 reference

Phenylalanine is the predominant antisickling agent in Cajanus cajan seed extract

straw mushroom

1 reference

Flavor Compounds in Straw MushroomsVolvariellavolvaceaHarvested at Different Stages of Maturity

Chlamydomonas reinhardtii

1 reference

The response of Chlamydomonas reinhardtii to nitrogen deprivation: a systems biology analysis

Saccharomyces cerevisiae

1 reference

Deletion of theSaccharomyces cerevisiae ARO8gene, encoding an aromatic amino acid transaminase, enhances phenylethanol production from glucose

Albugo candida

1 reference

Phytoalexins and polar metabolites from the oilseeds canola and rapeseed: differential metabolic responses to the biotroph Albugo candida and to abiotic stress

Allium cepa

1 reference

Antispasmodic saponins from bulbs of red onion, Allium cepa L. var. Tropea

Brassica rapa

1 reference

Sinalexin, a phytoalexin from white mustard elicited by destruxin B and Alternaria brassicae

Castanea sativa

1 reference

Relation métabolique entre l'arginine et l'acide γ-aminobutyrique dans le fruit de Castanea sativa: étude préliminaire de l'arginase

Claviceps purpurea

1 reference

Quantitative analysis of free amino acids of saprophytic cultures of Claviceps purpurea

Glinus oppositifolius

1 reference

L-(-)-(N-trans-Cinnamoyl)-arginine, an Acylamino Acid from Glinus oppositifolius (L.) Aug. DC

soybean

1 reference

Nitrogen-containing compounds ofGlycine hispida

Kaempferia parviflora

1 reference

Structures of two new phenolic glycosides, kaempferiaosides A and B, and hepatoprotective constituents from the rhizomes of Kaempferia parviflora

Colchicum trigynum

1 reference

Polypeptides and amino acids in the bulbus of Merendera caucasica

Hypholoma fasciculare

1 reference

Investigation on some compounds biosynthesized by fruitbodies of Naematoloma fasciculare/huds. ex fr./p. Karst

corroboree frog

1 reference

Notizen: Über eine alkaloidartige Substanz aus der Haut von Pseudophryne corroboree

Saussurea medusa

1 reference

Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa

Stellaria media

1 reference

Amino-acid and mineral composition of Stellaria media

Vigna unguiculata

1 reference

HYDROLYSIS OF VIGNIN OF THE COW-PEA (VIGNA SINENSIS)

Zyzzya fuliginosa

2 references

3,7-Dimethylguanine, a new purine from a Philippine sponge Zyzzya fuliginosa

Makaluvamines H-M and damirone C from the pohnpeian sponge Zyzzya fuliginosa

Atractylodes lancea

2 references

Glycosides of Atractylodes ovata

Glycosides of Atractylodes japonica.

Melissa officinalis

1 reference

Enzymes of phenylpropanoid metabolism in the important medicinal plant Melissa officinalis L.

Bryobium erioides

1 reference

Structures of two new phenolic glycosides, kaempferiaosides A and B, and hepatoprotective constituents from the rhizomes of Kaempferia parviflora

Cannabis sativa

1 reference

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

Bryobium eriaeoides

1 reference

Structures of two new phenolic glycosides, kaempferiaosides A and B, and hepatoprotective constituents from the rhizomes of Kaempferia parviflora

Caenorhabditis elegans

3 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

Network Architecture and Mutational Sensitivity of the C. elegans Metabolome.

Apium graveolens

1 reference

Phytochemical and biological characterization of Italian "sedano bianco di Sperlonga" Protected Geographical Indication celery ecotype: A multimethodological approach

common sunflower

1 reference

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

Beta vulgaris

1 reference

Betalainic and nutritional profiles of pigment-enriched red beet root (Beta vulgaris L.) dried extracts

Spinacia oleracea

2 references

A metabolomics study of ascorbic acid-induced in situ freezing tolerance in spinach (Spinacia oleracea L.).

Differences in the metabolite profiles of spinach (Spinacia oleracea L.) leaf in different concentrations of nitrate in the culture solution

Brassica oleracea

1 reference

Metabolic differentiation of diamondback moth ( Plutella xylostella (L.)) resistance in cabbage ( Brassica oleracea L. ssp. capitata).

Capsella bursa-pastoris

1 reference

Chemical composition and biological screening of Capsella bursa-pastoris

Phaseolus vulgaris

2 references

Metabolomics and Transcriptomics Identify Multiple Downstream Targets of Paraburkholderia phymatum σ54 During Symbiosis with Phaseolus vulgaris.

Metabolite Profiling of Root Exudates of Common Bean under Phosphorus Deficiency

broad bean

1 reference

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

Ginkgo biloba

1 reference

De novo transcriptome analysis revealed genes involved in flavonoid biosynthesis, transport and regulation in Ginkgo biloba

Perilla frutescens

1 reference

Intake of Alpha-Linolenic Acid-Rich Perilla frutescens Leaf Powder Decreases Home Blood Pressure and Serum Oxidized Low-Density Lipoprotein in Japanese Adults

Punica granatum

2 references

Exploitation of the health-promoting and sensory properties of organic pomegranate (Punica granatum L.) juice through lactic acid fermentation

Elucidating the role of shikimate dehydrogenase in controlling the production of anthocyanins and hydrolysable tannins in the outer peels of pomegranate

Oryza sativa

2 references

Assessment of nutritional value and quantitative analysis of bioactive phytochemicals through targeted LC-MS/MS method in selected scented and pigmented rice varietals

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

Triticum aestivum

2 references

Physiological and metabolome changes during anther development in wheat (Triticum aestivum L.).

Comparative metabolic responses and adaptive strategies of wheat (Triticum aestivum) to salt and alkali stress

Prunus avium

1 reference

Postharvest responses of sweet cherry fruit and stem tissues revealed by metabolomic profiling

Nicotiana tabacum

2 references

Nontargeted metabolite profiling in compatible pathogen-inoculated tobacco (Nicotiana tabacum L. cv. Wisconsin 38) using UPLC-Q-TOF/MS.

Metabolic profiling of Chinese tobacco leaf of different geographical origins by GC-MS

chia

1 reference

Amino acids and fatty acids profile of chia (Salvia hispanica L.) and flax (Linum usitatissimum L.) seed

Taraxacum mongolicum

1 reference

Chemical constituents of Taraxacum formosanum

Escherichia coli

3 references

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

Regulator Gene Controlling Enzymes Concerned in Tyrosine Biosynthesis in Escherichia coli

Introduction of two mutations into AroG increases phenylalanine production in Escherichia coli.

Sinorhizobium meliloti

1 reference

Creation and Characterization of a Genomically Hybrid Strain in the Nitrogen-Fixing Symbiotic Bacterium Sinorhizobium meliloti

0 references

0 references

Armenian Soviet Encyclopedia

0 references

1 reference

C29601

1 reference

InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/s1

14 February 2018

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L-Phenylalanine

0 references

Identifiers

InChI

1 reference

L-phenylalanine (English)

19 October 2016

2 references

L-phenylalanine (English)

19 October 2016

14 February 2018

3 references

L-phenylalanine (English)

19 October 2016

14 February 2018

https://commonchemistry.cas.org/detail?cas_rn=63-91-2

9 April 2021

1 reference

L-(-)-Phenylalanine (English)

19 October 2016

2 references

L-phenylalanine (English)

19 October 2016

6925665

1 reference

Reaxys registry number

1910408

1 reference

L-phenylalanine (English)

19 October 2016

Gmelin number

50837

0 references

1 reference

L-PHENYLALANINE (English)

19 October 2016

2 references

inferred from InChIKey

MSBNK-BGC_Munich-RP000401

1 reference

MassBank accession ID

0 references

MSBNK-BGC_Munich-RP000402

0 references

MSBNK-BGC_Munich-RP000403

0 references

MSBNK-BGC_Munich-RP000411

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MSBNK-BGC_Munich-RP000412

0 references

MSBNK-Keio_Univ-KO003666

0 references

MSBNK-Keio_Univ-KO003667

0 references

MSBNK-Keio_Univ-KO003668

0 references

MSBNK-Keio_Univ-KO003669

0 references

MSBNK-Keio_Univ-KO003670

0 references

MSBNK-Metabolon-MT000018

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000036

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000037

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000038

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000039

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000040

0 references

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MSBNK-Osaka_Univ-OUF00320

0 references

MSBNK-Osaka_Univ-OUF01009

0 references

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MSBNK-GL_Sciences_Inc-GLS00057

0 references

MSBNK-IPB_Halle-PB006064

0 references

MSBNK-IPB_Halle-PB006065

0 references

MSBNK-IPB_Halle-PB006081

0 references

MSBNK-Kazusa-KZ000052

0 references

MSBNK-Keio_Univ-KO001563

0 references

MSBNK-Keio_Univ-KO001564

0 references

MSBNK-Keio_Univ-KO001565

0 references

MSBNK-Keio_Univ-KO001566

0 references

MSBNK-Keio_Univ-KO001567

0 references

SPLASH

splash10-00di-0900000000-99b1e46c9ca3032be112

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splash10-00di-0900000000-c068f70074d7ced6b8b1

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splash10-00di-0900000000-48fb6ee11fb845efdcf3

0 references

splash10-0fr6-1930000000-a37fbccaf826443ef70c

0 references

splash10-03di-0900000000-80558c17dc1845663c85

0 references

splash10-0002-3900000000-e1ee31d41e48824e84b7

0 references

splash10-0f6x-9500000000-cc11290a37615f24e16e

0 references

splash10-0006-9000000000-1a6020bce0e1a9a14832

0 references

splash10-0006-9000000000-38c044a112152626962e

0 references

splash10-014i-0900000000-9b908abfcb63153d60b3

0 references

splash10-00di-1900000000-3ba5964e151bb1d56188

0 references

splash10-00di-2900000000-20a7d24da0281f5b3b78

0 references

splash10-0udi-5900000000-99329db3f395a4f3d593

0 references

splash10-0fb9-9300000000-e3023e2a20fe1c5fe987

0 references

splash10-00di-0900000000-1d714b1667871b7d7e82

0 references

splash10-00di-0900000000-1dd00f428846031939fd

0 references

splash10-00di-0900000000-cf90e5631705754e390f

0 references

splash10-00di-0900000000-88d4b01f6ee598453af9

0 references

splash10-00di-0900000000-20a2bb1d995a8486141c

0 references

splash10-014i-0900000000-45cacc3b6bf55e07c8cd

0 references

splash10-014i-0900000000-5f5b13d6becdc1eeedc2

0 references

splash10-0f6x-9600000000-b8320b3046aea4d76c6a

0 references

splash10-00di-0900000000-0c25a5c116eac7bb059b

0 references

splash10-00di-0900000000-2804f79084ac4e67e155

0 references

splash10-014i-0900000000-8a71bb1f8424064d7caf

0 references

splash10-0f6x-9800000000-e027ff6bb67ce55e80a5

0 references

splash10-014i-0900000000-9f6185e9c7d54189f369

0 references

splash10-00di-0900000000-df5f72fe2bba91742427

0 references

splash10-0ir3-0988735721-51af246c5e307624d6a4

0 references

splash10-0002-0900000000-37833998cb13dd974fc1

0 references

splash10-014l-1940000000-537e2725d621246630c1

0 references

splash10-0ul9-3659000000-b85be4e71798e2fdc47b

0 references

splash10-00di-9630000000-ead0919f9a19d2352d80

0 references

splash10-014i-0900000000-cb4f1e3bde1f29e264f5

0 references

splash10-014i-0900000000-2ab526c45d7503001dc3

0 references

splash10-01b9-0900000000-ddc97bf483f1a3361fd7

0 references

splash10-01ot-1900000000-8dbbc0673f81b8e1de2a

0 references

splash10-014i-0900000000-c6e85980af17ca8821b4

0 references

splash10-00di-0900000000-57b523f41de2e542f2e6

0 references

splash10-00di-0900000000-cb14d5ccf75ccf24513b

0 references

splash10-0uk9-3900000000-8910b46279c99b817008

0 references

splash10-0ufr-7900000000-6f14a1b3e0334da42e5e

0 references

splash10-0fb9-9500000000-dd8c597f1e542b911e9f

0 references

splash10-014l-2960000000-f77489792f0652dd5613

0 references

splash10-004i-9300000000-08c642dab7f49c00da43

0 references

splash10-00di-2900000000-cb2d6dc4bf9515150328

0 references

splash10-0gb9-2900000000-c14d44c8a67621757f3d

0 references

splash10-014i-0900000000-0f3b994108b8a9fd2a56

0 references

0 references

1 reference

Hazardous Substances Data Bank

28 October 2019

(L)-Phenylalanine (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

UNII

47E5O17Y3R

ECHA Substance Infocard ID

14 February 2018

100.000.517

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.000.517

27 December 2018

Guide to Pharmacology Ligand ID

3-phenyl-L-alanine (English)

quotation

CAS no.: 63-91-2 (English)

FL number

17.018

1 reference

quotation

CAS no.: 63-91-2 (English)

23 January 2021

17.018

1 reference

28 December 2019

PHENYLALANINE (English)

quotation

CAS no.: 63-91-2 (English)

3313

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

3313

L-phenylalanine (English)

19 October 2016

Phenylalanine

0 references

0 references

0 references

0 references

1 reference

14 February 2018

1 reference

Human Metabolome Database ID

HMDB0000159

2 references

based on heuristic

inferred from InChIKey

1 reference

L-phenylalanine (English)

19 October 2016

UNII

47E5O17Y3R

1 reference

0 references

0 references

1 reference

1 reference

Brockhaus Enzyklopädie online ID

L-phenylalanine (English)

19 October 2016

0 references

0 references

0 references

0 references

1 reference

28 October 2013

Gran Enciclopèdia Catalana ID

fenilalanina

0 references

Gran Enciclopèdia Catalana ID (former scheme)

0108552

0 references

Great Russian Encyclopedia portal ID

fenilalanin-37e232

0 references

JECFA number

1428

1 reference

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

13 May 2021

1 reference

9 July 2020

Microsoft Academic ID

0 references

1 reference

26 January 2022

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

Store norske leksikon ID

fenylalanin

0 references

WikiSkripta article ID

58774

0 references

WordNet 3.1 Synset ID

15006138-n

1 reference