(Q4637160)

4-hydroxyphenylacetic acid (English)

19 October 2016

chemical formula

C₈H₈O₃

1 reference

4-hydroxyphenylacetic acid (English)

19 October 2016

canonical SMILES

C1=CC(=CC=C1CC(=O)O)O

1 reference

4-hydroxyphenylacetic acid (English)

19 October 2016

melting point

149.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Guanomyces polythrix

1 reference

Phytotoxic naphthopyranone derivatives from the coprophilous fungus Guanomyces polythrix.

Ranunculus ficaria

1 reference

Polyphenolic Compounds from Flowers of Hibiscus

Lupinus angustifolius

1 reference

Phenolic compounds isolated from bitter lupine seeds and their inhibitory effects on germination and seedling growth of lettuce

Isatis tinctoria

1 reference

Acid constituents from Isatis tinctoria

Vaccinium macrocarpon

1 reference

Separation, characterization, and quantitation of benzoic and phenolic antioxidants in American cranberry fruit by GC-MS.

Secamone afzelii

1 reference

Phenolic acids in leaves of Secamone afzelii (Rhoem.) Schult. (Asclepiadaceae)

Oenothera biennis

1 reference

The phenolic acids of some species of the Oenothera L. genus

Oenothera lamarckiana

1 reference

The phenolic acids of some species of the Oenothera L. genus

Althaea officinalis

2 references

Chromatographic Investigations of Phenolic Acids and Coumarins in the Leaves and Flowers of Some Species of the Genus Althaea

Flavonoids, Phenolic Acids and Coumarins from the Roots of Althaea officinalis

Althaea armeniaca

1 reference

Chromatographic Investigations of Phenolic Acids and Coumarins in the Leaves and Flowers of Some Species of the Genus Althaea

Althaea cannabina

1 reference

Chromatographic Investigations of Phenolic Acids and Coumarins in the Leaves and Flowers of Some Species of the Genus Althaea

Althaea narbonensis

1 reference

Chromatographic Investigations of Phenolic Acids and Coumarins in the Leaves and Flowers of Some Species of the Genus Althaea

Althaea broussonetiifolia

1 reference

Chromatographic Investigations of Phenolic Acids and Coumarins in the Leaves and Flowers of Some Species of the Genus Althaea

Phycopsis

1 reference

Phycopsisenone, a New Phenolic Secondary Metabolite from the Sponge Phycopsis sp.

Packera bellidifolia

1 reference

Chemical constituents of Packera coahuilensis and Packera bellidifolia

moringata pitosa

1 reference

Mutagens from roasted seeds of Moringa oleifera

Homo sapiens

3 references

Physiological and environmental parameters associated with mass spectrometry-based salivary metabolomic profiles

Recon 2.2: from reconstruction to model of human metabolism

A community-driven global reconstruction of human metabolism.

Stachylidium

1 reference

Stachylines A-D from the sponge-derived fungus Stachylidium sp.

Ophiocordyceps sinensis

1 reference

Anti-inflammatory principles from Cordyceps sinensis

Forsythia viridissima

1 reference

Chemical constituents from the fruits of Forsythia suspensa and their antimicrobial activity.

Pinus pinaster

1 reference

Carboxylic Acids of Moroccan Pinus Pinaster Bark Extract

Olea europaea

5 references

High-performance liquid chromatography of selected phenolic compounds in olive oils

Antioxidant Capacity and Phenolic Profile of Table Olives from the Greek Market

Biophenolic components of olives

Phenolic compounds of virgin olive oil: influence of paste preparation techniques

Retention and distribution of natural antioxidants (α-tocopherol, polyphenols and terpenic acids) after shallow frying of vegetables in virgin olive oil

Forsythia suspensa

3 references

New Quinoid Glycosides from Forsythia suspensa

A new lignan glycoside from Forsythia suspensa

Quinoid glycosides from Forsythia suspensa

Mycale mytilorum

1 reference

Chemical investigation of Mycale mytilorum and a study on toxicity and antidiabetic activity of 5-octadecylpyrrole-2-carboxaldehyde

Cichorium intybus

1 reference

Guaianolides from Cichorium intybus and structure revision of Cichorium sesquiterpene lactones

Taraxacum formosanum

1 reference

Chemical Constituents of Taraxacum formosanum.

Sargentodoxa cuneata

1 reference

Chemical Constituents of the Stem of Sargentodoxa cuneata

Tragopogon orientalis

1 reference

Phytochemical studies of the herb, Tragopogon orientalis L. (Asteraceae). 2. Components of a methanol extract

Grosmannia crassivaginata

1 reference

Phenolic and polyketide metabolites of the aspen blue stain fungus Ophiostoma crassivaginata

Penicillium herquei

2 references

Hualyzin, a symmetrical urea derivative isolated from Penicillium herquei isolate GA4.

Hualyzin, a symmetrical urea derivative isolated from Penicillium herquei isolate GA4.

Seuratia

1 reference

Phycopsisenone, a New Phenolic Secondary Metabolite from the Sponge Phycopsis sp.

Avena sativa

1 reference

Free, esterified, and insoluble-bound phenolic acids. 3. Composition of phenolic acids in cereal and potato flours

Oryza sativa

1 reference

Free, esterified, and insoluble-bound phenolic acids. 3. Composition of phenolic acids in cereal and potato flours

Triticum aestivum

1 reference

Free, esterified, and insoluble-bound phenolic acids. 3. Composition of phenolic acids in cereal and potato flours

Vitis vinifera

1 reference

RP-HPLC analysis of phenolic compounds and flavonoids in beverages and plant extracts using a CoulArray detector.

maize

1 reference

Free, esterified, and insoluble-bound phenolic acids. 3. Composition of phenolic acids in cereal and potato flours

Arbutus unedo

1 reference

Chemical Composition of Fatty Acid and Unsaponifiable Fractions of Leaves, Stems and Roots of Arbutus unedo and in vitro Antimicrobial Activity of Unsaponifiable Extracts

Ceratocystis ips

1 reference

The chemistry of the blue stain fungi. Part 1. Some metabolites of Ceratocystis species associated with mountain pine beetle infected lodgepole pine

Drypetes gossweileri

1 reference

Chemical constituents of Drypetes gossweileri and their enzyme inhibitory and anti-fungal activities

Epichloe typhina

1 reference

Three phenolic acid derivatives from stromata of Epichloe typhina on Phleum pratense

Penicillium javanicum

1 reference

New Dioxomorpholine Derivatives, Javanicunine A and B, from Eupenicillium javanicum

Rhizoctonia solani

1 reference

Studies on Metabolic Products of Hypochnus sasakii Shirai

Penicillium chrysogenum

1 reference

Cerebrosides and 2-Pyridone Alkaloids from the Halotolerant FungusPenicillium chrysogenumGrown in a Hypersaline Medium

Pteroxygonum giraldii

1 reference

A New Triterpene and Phenolic Compounds from the Roots of Pteroxygonum giraldii

Zyzzya fuliginosa

1 reference

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

Spencermartinsia viticola

1 reference

Spencertoxin and spencer acid, new phytotoxic derivatives of diacrylic acid and dipyridinbutan-1,4-diol produced by Spencermartinsia viticola , a causal agent of grapevine Botryosphaeria dieback in Australia

Opuntia streptacantha

1 reference

Anti-hyperglycemic effect of Opuntia streptacantha Lem.

Moringa pterygosperma

1 reference

Mutagens from roasted seeds of Moringa oleifera

Caenorhabditis elegans

1 reference

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

Senecio scandens

1 reference

Authentication of Senecio scandens and S. vulgaris based on the comprehensive secondary metabolic patterns gained by UPLC-DAD/ESI-MS

Oenothera grandiflora

1 reference

The phenolic acids of some species of the Oenothera L. genus

Oenothera erythrosepala

1 reference

The phenolic acids of some species of the Oenothera L. genus

Tragopogon pratensis

1 reference

Phytochemical studies of the herb, Tragopogon orientalis L. (Asteraceae). 2. Components of a methanol extract

Taraxacum mongolicum

1 reference

Chemical Constituents of Taraxacum formosanum.

Oenothera glazioviana

1 reference

The phenolic acids of some species of the Oenothera L. genus

Identifiers

InChI

InChI=1S/C8H8O3/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11)

1 reference

4-hydroxyphenylacetic acid (English)

XQXPVVBIMDBYFF-UHFFFAOYSA-N

19 October 2016

InChIKey

2 references

4-hydroxyphenylacetic acid (English)

19 October 2016

ChEBI release 2020-09-01

2 references

4-hydroxyphenylacetic acid (English)

XQXPVVBIMDBYFF-UHFFFAOYSA-N

19 October 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=156-38-7

1 reference

4-hydroxyphenylacetic acid (English)

19 October 2016

1 reference

4-hydroxyphenylacetic acid (English)

19 October 2016

Reaxys registry number

1448766

1 reference

4-hydroxyphenylacetic acid (English)

19 October 2016

ChEBI ID

18101

mapping relation type

2 references

4-hydroxyphenylacetic acid (English)

19 October 2016

ChEBI release 2019-10-02

1 reference

MSBNK-Fac_Eng_Univ_Tokyo-JP003520

CHEMBL1772 (English)

19 October 2016

1 reference

MassBank accession ID

0 references

MSBNK-GL_Sciences_Inc-GLS00020

0 references

MSBNK-Osaka_Univ-OUF00067

0 references

MSBNK-RIKEN-PR010008

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP007234

0 references

MSBNK-Keio_Univ-KO000968

0 references

MSBNK-Keio_Univ-KO000969

0 references

MSBNK-Keio_Univ-KO000970

0 references

MSBNK-Keio_Univ-KO000971

0 references

MSBNK-Keio_Univ-KO000972

0 references

MSBNK-Kazusa-KZ000008

0 references

MSBNK-Kazusa-KZ000101

0 references

SPLASH

splash10-0a4i-6900000000-fdb73325a31c758496e9

0 references

splash10-0gyk-0980000000-ed36f36969e4d51b9a8d

0 references

splash10-01ta-1930000000-57c9e8ddaa10569055aa

0 references

splash10-0h01-0940000000-a14203384331e709252f

0 references

splash10-0zfr-0900000000-369a695f2c7bcf3a4a5c

0 references

splash10-0a4i-4900000000-88da569804a98e1a99ea

0 references

splash10-0a4i-9300000000-eef23e2f30d876f4a1f9

0 references

splash10-0a4i-9000000000-0a95379b7cea57386b0b

0 references

splash10-0a4i-9000000000-dd0a48d9d6528f6a0a6a

0 references

splash10-03fs-1930000000-80c21819072fb01958dc

0 references

splash10-00di-9410000000-678591f03aba45c2a6ae

0 references

splash10-0a4i-0900000000-5262f048c86169599d1a

0 references

splash10-0a4i-0900000000-4915e754d2d0ee23dd0b

0 references

splash10-0a4i-1900000000-067dca59d03e9d49c2a1

0 references

splash10-0a4i-1900000000-013c13fb40688a343897

0 references

splash10-03dl-5900000000-2ec63b81ae076679cebf

0 references

splash10-00xr-9000000000-1588a41bbc8948ae38f2

0 references

splash10-03fs-1931100000-50456fed0c5ef95ecb57

0 references

splash10-0h0r-2940000000-760b6c506072a61059c0

0 references

splash10-0pb9-0900000000-e3dfb4b180d858b3a854

0 references

splash10-0kdl-9400000000-35ecc22161defddc7b21

0 references

splash10-056r-9400000000-9a6cb39e019a0b40a666

0 references

splash10-0a4i-3900000000-3be1d4a7c16ea7a3eee1

0 references

DSSTox substance ID

DTXSID5059745

1 reference

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

DSSTOX compound identifier

0 references

0 references

0 references

205-851-3

1 reference

imported from Wikimedia project

English Wikipedia

ECHA Substance Infocard ID

100.005.321

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.005.321

27 December 2018

AICS Chemical ID (BEING DELETED)

p-hydroxyphenylacetic acid (English)

quotation

CAS no.: 156-38-7 (English)

1 reference

0 references

4098

0 references

Human Metabolome Database ID

HMDB0000020

1 reference

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00050490

1 reference

based on heuristic

inferred from InChIKey

Natural Product Atlas ID

NPA032547

1 reference

based on heuristic

inferred from InChIKey

0 references

0 references

0 references

1 reference

28 October 2013

Microsoft Academic ID

0 references

1 reference

1AI6 (English)

19 October 2016

1 reference

3PCG (English)

19 October 2016

1 reference

2YAJ (English)

19 October 2016

1 reference

5AIP (English)

19 October 2016

1 reference

2JBT (English)

19 October 2016

1 reference

2YYJ (English)

19 October 2016

1 reference

2YYM (English)