(Q416446)

Gene Ontology release 2019-11-16

hydroquinone glucosyltransferase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

Arbutin structure.svg
620 × 464; 13 KB

1 reference

German Wikipedia

mass

272.089603 dalton

1 reference

(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol

arbutin (English)

5 October 2016

1 reference

1 reference

based on heuristic

inferred from InChI

(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₂H₁₆O₇

1 reference

arbutin (English)

19 November 2016

C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O

1 reference

arbutin (English)

19 November 2016

C1=CC(=CC=C1O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O

1 reference

arbutin (English)

19 November 2016

199.5 degree Celsius

1 reference

Russian Wikipedia

198 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

safety classification and labelling

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

NFPA Health

0

NFPA Fire

0

NFPA Instability

0

1 reference

Sesquiterpenes and other constituents from chilean mutisieae

1 reference

Camellia sinensis

1 reference

Coffea arabica

1 reference

Triticum aestivum

1 reference

Myrothamnus flabellifolia

2 references

Arbutin and sucrose in the leaves of the resurrection plant Myrothamnus flabellifolia

Qualitative and quantitative phytochemical characterization of Myrothamnus flabellifolia Welw

Onobrychis bobrovii

1 reference

Polyphenols ofOnobrychis bobrovii

Breynia officinalis

1 reference

Terpenic and phenolic glycosides from leaves of Breynia officinalis HEMSL.

Cotoneaster simonsii

1 reference

Flavonols and isoflavones from Cotoneaster simonsii

Escherichia coli

2 references

Cellobiose-6-Phosphate Hydrolase (CelF) ofEscherichia coli: Characterization and Assignment to the Unusual Family 4 of Glycosylhydrolases

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

Veronica turrilliana

1 reference

Phenylethanoids, iridoids and a spirostanol saponin from Veronica turrilliana

Aesculus californica

1 reference

Phenolic constituents of California buckeye fruit

Antennaria microphylla

1 reference

Allelopathy of Small Everlasting (Antennaria microphylla): Identification of Constituents Phytotoxic to Leafy Spurge (Euphorbia esula)

Arbutus andrachne

1 reference

ARBUTUS ANDRACHNE

Arctostaphylos canescens

1 reference

Studies of cuticle drugs from natural sources. IV. Inhibitory effects of some Arctostaphylos plants on melanin biosynthesis

Arctostaphylos columbiana

2 references

Phytochemical Investigation of Arctostaphylos columbiana Piper and Arctostaphylos patula Greene (Ericaceae)

Studies of cuticle drugs from natural sources. IV. Inhibitory effects of some Arctostaphylos plants on melanin biosynthesis

Arctostaphylos nevadensis

1 reference

Studies of cuticle drugs from natural sources. IV. Inhibitory effects of some Arctostaphylos plants on melanin biosynthesis

Arctostaphylos patula

2 references

Phytochemical Investigation of Arctostaphylos columbiana Piper and Arctostaphylos patula Greene (Ericaceae)

Studies of cuticle drugs from natural sources. IV. Inhibitory effects of some Arctostaphylos plants on melanin biosynthesis

Arctostaphylos viscida

1 reference

Studies of cuticle drugs from natural sources. IV. Inhibitory effects of some Arctostaphylos plants on melanin biosynthesis

Betula platyphylla

1 reference

Four glucosides ofp-hydroxyphenyl derivatives from birch leaves

Calluna vulgaris

1 reference

Phenolic composition and its seasonal variation in Calluna vulgaris

Cuscuta chinensis

1 reference

An alkaloid and two lignans fromCuscuta chinensis

Eriosema tuberosum

1 reference

Phenolic glycosides from Eriosema tuberosum

Huperzia serrata

1 reference

A new alkaloid and arbutin from the whole plant of Huperzia serrata

Mutisia acuminata

2 references

New chromone, coumarin, and coumestan derivatives from Mutisia acuminata var. hirsuta

Chemical Investigation of the Aerial Parts of Mutisia Acuminata

Mutisia oligodon

1 reference

Highly oxygenated sesquiterpenes from Polyachyrus sphaerocephalus and further constituents from chilean mutisieae

Myrsine seguinii

2 references

Hydroquinone glycosides from leaves of Myrsine seguinii

Myrseguinosides A-E, Five New Glycosides from the Fruits of Myrsine seguinii

Onobrychis arenaria

2 references

Flavonoids of the epigeal part ofOnobrychis arenaria

Flavonoids from the aerial parts of Satureja khuzestanica

Onobrychis kachetica

1 reference

Onobrychis meschetica

1 reference

Onobrychis radiata

1 reference

Onobrychis cyri

1 reference

Polyphenols, condensed tannins, and other natural products in Onobrychis viciifolia (Sainfoin).

Onobrychis viciifolia

1 reference

Polyphenols, condensed tannins, and other natural products in Onobrychis viciifolia (Sainfoin).

marjoram

1 reference

Preliminary study of phenolic glycosides from Origanum majorana; quantitative estimation of arbutin; cytotoxic activity of hydroquinone

Picrasma quassioides

1 reference

Phenylpropanoids and other secondary metabolites from fresh fruits of Picrasma quassioides

Rauvolfia serpentina

1 reference

High-Yield Formation of Arbutin from Hydroquinone by Cell-Suspension Cultures ofRauwolfia serpentina

Rhodiola coccinea

1 reference

6-O-galloylarbutin fromRhodiola coccinea

Rhodiola sacra

2 references

Active-oxygen scavenging activity of traditional nourishing-tonic herbal medicines and active constituents of Rhodiola sacra

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sacra S. H. Fu.

Semiarundinaria fastuosa

1 reference

Constituents of Bamboos and Bamboo Grasses

Stratiotes aloides

1 reference

Flavonoid glucuronides and a chromone from the aquatic macrophyte Stratiotes aloides

Vaccinium erythrocarpum

1 reference

Influence of ecological factors on the amount of active substances in the leaves of the mountain cranberry

Vaccinium pallidum

1 reference

Isolation of isopyroside from Vaccinium vacillans

Vaccinium vacillans

1 reference

Isolation of isopyroside from Vaccinium vacillans

Viburnum dilatatum

1 reference

Phenolic glycosides from Viburnum dilatatum

Viburnum phlebotrichum

1 reference

Phlebotrichin, a phenolic compound from the fresh leaves of Viburnum phlebotrichum

Viburnum rhytidophyllum

1 reference

VIBURNINE, A MACROCYCLIC SPERMIDINE ALKALOID FROM VIBURNUM RHYTIDOPHYLLUM

Viburnum wrightii

1 reference

A phenol alloside from viburnum wrightii

Viola arvensis

1 reference

HPLC Analysis of Phenolic Compounds in Field Violet

Zanthoxylum bungeanum

1 reference

Flavonol glucosides in pericarps of Zanthoxylum bungeanum

Zanthoxylum piperitum

1 reference

Antioxidative activity in the pericarp and seed of Japanese pepper (Xanthoxylum piperitum DC)

Arbutus unedo

1 reference

Phenolics of Arbutus unedo L. (Ericaceae) fruits: identification of anthocyanins and gallic acid derivatives.

Breynia fruticosa

1 reference

Glycosides from Breynia fruticosa and Breynia rostrata

Broussonetia papyrifera

1 reference

Antioxidant phenolics from Broussonetia papyrifera fruits

Centaurea urvillei

1 reference

Phenolic Glycosides with antiproteasomal activity from Centaurea urvillei DC. subsp. urvillei

Cephalanthus occidentalis

1 reference

Six new triterpenoid saponins from the root and stem bark of Cephalanthus occidentalis

Oreoseris gossypina

1 reference

Benzofuran Derivatives fromGerbera saxatilis

Grevillea robusta

1 reference

Phenolic constituents from Grevillea robusta

Halocarpus biformis

1 reference

The glycosidic precursor of (Z)-5-ethylidene-2(5H)-furanone in Halocarpus biformis juvenile foliage

Juniperus communis

1 reference

New phenylpropanoid glycosides from Juniperus communis var. depressa

Juniperus communis depressa

1 reference

New phenylpropanoid glycosides from Juniperus communis var. depressa

Juniperus communis var. depressa

1 reference

New phenylpropanoid glycosides from Juniperus communis var. depressa

Mutisia orbignyana

1 reference

Further 5-methylcoumarin derivatives from Mutisia orbignyana

Paederia foetida

1 reference

Studies on the Constituents of Paederia chinensis HANCE

Pyrus calleryana

1 reference

Phenolic metabolites from Pyruscalleryana and evaluation of its free radical scavenging activity.

Rhodiola kirilowii

1 reference

New compounds from Rhodiola kirilowii

Salvia rhyacophila

1 reference

7-epi-rhyacophiline, a 5,6-secoclerodane diterpene from Salvia rhyacophila

Senecio mairetianus

1 reference

Eremophilanes from Senecio mairetianus and some reaction products

Klasea radiata

1 reference

The content of arbutin in some species of the genusSerratula

potato

1 reference

Changes in the accumulation of soluble and cell wall-bound phenolics in elicitor-treated cell suspension cultures and fungus-infected leaves of Solanum tuberosum

Thymus vulgaris

1 reference

New monoterpene glucoside from the aerial parts of thyme (Thymus vulgaris L.).

Turnera diffusa

1 reference

Phytochemical investigation of Turnera diffusa

Vaccinium dunalianum

1 reference

Caffeoyl arbutin and related compounds from the buds of Vaccinium dunalianum

1 reference

1 reference

Phenolic Compounds from Atriplex littoralis and Their Radiation-Mitigating Activity

Nelumbo nucifera

1 reference

Rat lens aldose reductase inhibitory constituents of Nelumbo nucifera stamens

Onobrychis michauxii

1 reference

Myrothamnus flabellifolius

2 references

Arbutin and sucrose in the leaves of the resurrection plant Myrothamnus flabellifolia

Qualitative and quantitative phytochemical characterization of Myrothamnus flabellifolia Welw

Sedum takesimense

1 reference

Anti-oxidant constituents from Sedum takesimense

Arctostaphylos uva-ursi

10 references

Quantitative determination of biologically active constituents in medicinal plant crude extracts by thin-layer chromatography—densitometry

HPLC Analysis of Phenolics and Flavonoids inArctostaphylos uvae-ursi

A single extraction step in the quantitative analysis of arbutin in bearberry (Arctostaphylos uva-ursi) leaves by high-performance liquid chromatography

In Vitro-Cultures of Arctostaphylos-Species. III: Phytochemical Comparison of in Vitro-Cultures and Outdoor Plants

Pharmacological studies on leaf of Arctostaphylos uva-ursi (L.) Spreng. IV. Effect of 50% methanolic extract from Arctostaphylos uva-ursi (L.) Spreng. (bearberry leaf) on melanin synthesis

Isolation of Piceoside from Arctostaphylos uva-ursi

Pharmacological Studies on Leaf of Arctostaphylos uva-ursi (L.) SPRENG. I. Combined Effect of 50% Methanolic Extract from Arctostaphylos uva-ursi (L.) SPRENG. (Bearberry Leaf) and Prednisolone on Immuno-inflammation

Pharmacological studies on leaf of Arctostaphylos uva-ursi (L.) Spreng. III. Combined effect of arbutin and indomethacin on immuno-inflammation

Studies of cuticle drugs from natural sources. IV. Inhibitory effects of some Arctostaphylos plants on melanin biosynthesis

Determination of arbutin in uvae-ursi folium (bearberry leaves) by capillary zone electrophoresis

Vaccinium arctostaphylos

1 reference

An antidiabetic compound from Vaccinium arctostaphylos berries

Vaccinium hirtum var. koreanum

1 reference

Phenolic compounds of the leaves of Vaccinium arctostaphylos

Centaurea raphanina

1 reference

Phenolic Glycosides with antiproteasomal activity from Centaurea urvillei DC. subsp. urvillei

Cashew

1 reference

Tyrosinase inhibitors from Anacardium occidentale fruits

Lespedeza cyrtobotrya

1 reference

Melanin synthesis inhibitors from Lespedeza cyrtobotrya

Pyrus bourgaeana

1 reference

New benzyl alcohol glycosides from Pyrus bourgaeana

Phedimus kamtschaticus

1 reference

Anti-oxidant constituents from Sedum takesimense

Breynia vitis-idaea

1 reference

Terpenic and phenolic glycosides from leaves of Breynia officinalis HEMSL.

Pyrus communis

2 references

Chemical constituents from Commelina communis

Hylotelephium ewersii

1 reference

Flavonoids and hydroxycoumarins of Sedum ewersii

Piloselloides hirsuta

1 reference

Examination of coumarins, flavonoids and polysaccharopeptide for antibacterial activity

Casearia multinervosa

1 reference

New phenolic glycosides from the stems and leaves of Casearia multinervosa

Thalassotalea

1 reference

N-Acyl Dehydrotyrosines, Tyrosinase Inhibitors from the Marine Bacterium Thalassotalea sp. PP2-459.

physically interacts with

taste receptor type 2

subject has role

agonist

2 references

The Molecular Receptive Ranges of Human TAS2R Bitter Taste Receptors

Characterization of the beta-D-glucopyranoside binding site of the human bitter taste receptor hTAS2R16.

1 reference

0 references

0 references

Arbutin

0 references

Identifiers

InChI

InChI=1S/C12H16O7/c13-5-8-9(15)10(16)11(17)12(19-8)18-7-3-1-6(14)2-4-7/h1-4,8-17H,5H2/t8-,9-,10+,11-,12-/m1/s1

1 reference

arbutin (English)

19 November 2016

2 references

arbutin (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

497-76-7

2 references

arbutin (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=497-76-7

8 April 2021

1 reference

Arbutin (English)

19 November 2016

2 references

arbutin (English)

19 November 2016

Reaxys registry number

89673

1 reference

hydroquinone O-beta-D-glucopyranoside (English)

5 October 2016

ChEBI ID

18305

mapping relation type

2 references

ARBUTIN (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C12H16O7/c13-5-8-9(15)10(16)11(17)12(19-8)18-7-3-1-6(14)2-4-7/h1-4,8-17H,5H2/t8-,9-,10+,11-,12-/m1/s1

1 reference

ARBUTIN (English)

19 November 2016

2 references

inferred from InChIKey

Biological Magnetic Resonance Data Bank

1 reference

1 reference

BMRB ID

bmse000365

splash10-0229-0910000000-b31d757ca488939b3cd4

SPLASH

0 references

splash10-001i-0950000000-7ed72e8f18f67995ec19

0 references

splash10-001i-0950000000-4e4b52619c62fcd19f1d

0 references

splash10-016r-0290000000-ac1c71959cc3e8ae7248

0 references

splash10-016r-0390000000-cc2d6b65b6bdd7cbe310

0 references

splash10-0002-0090000000-a7028a3a9618849334b7

0 references

splash10-0uxs-0940000000-9984522469f86670798f

0 references

NMRShiftDB structure ID

40248272

1 reference

RTECS number

CE8663000

1 reference

Hazardous Substances Data Bank

1 reference

28 October 2019

ARBUTIN (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

arbutin (English)

ECHA Substance Infocard ID

19 November 2016

100.007.138

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.007.138

27 December 2018

4-hydroxyphenyl β-D-glucopyranoside (English)

quotation

CAS no.: 497-76-7 (English)

1 reference

28 December 2019

ARBUTIN (English)

CAS no.: 497-76-7 (English)

MeSH descriptor ID

D001104

subject named as

Arbutin

0 references

0 references

1 reference

arbutin (English)

19 November 2016

1 reference

Human Metabolome Database ID

HMDB0029943

2 references

based on heuristic

inferred from InChIKey

1 reference

hydroquinone O-beta-D-glucopyranoside (English)

5 October 2016

2 references

arbutin (English)

19 November 2016

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

0 references

1 reference

0 references

1 reference

28 October 2013

Microsoft Academic ID

0 references

1 reference

26 January 2022

1 reference

1 reference

agricultural-and-biological-sciences/arbutin

German Wikipedia

ScienceDirect topic ID

0 references

Store norske leksikon ID

0 references

1 reference

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023