(Q15426984)

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

Scopolin structure.svg
695 × 385; 28 KB

0 references

mass

354.095082±0 dalton

1 reference

6-methoxy-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one

Scopolin (English)

4 October 2016

2 references

inferred from InChIKey

6-methoxy-7-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one

inferred from InChI

2 references

inferred from InChIKey

6-methoxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one

inferred from InChI

1 reference

6-methoxy-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one

inferred from InChIKey

1 reference

inferred from InChI

chemical formula

C₁₆H₁₈O₉

1 reference

Scopolin (English)

4 October 2016

COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O

1 reference

Scopolin (English)

4 October 2016

COC1=C(C=C2C(=C1)C=CC(=O)O2)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O

1 reference

Components ofPtarmica bisserata

Scopolin (English)

4 October 2016

2 references

Coumarins ofPtarmica bisserata

Inulanthera nuda

1 reference

Phenols, Acetylenes, and Sesquiterpene Lactones fromInulanthera nuda

Aesculus pavia

2 references

Cytotoxic triterpenoid saponins from the fruits of Aesculus pavia L.

Cytotoxic triterpenoid saponins from the fruits of Aesculus pavia L.

Artemisia minor

2 references

Chemical constituents from the aerial parts of Artemisia minor.

Chemical Constituents of the Aerial Parts of Artemisia iwayomogi

Baptisia arachnifera

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia bracteata

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia calycosa

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia cinerea

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia lanceolata

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia nuttalliana

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia perfoliata

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia simplicifolia

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia tinctoria

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Erycibe obtusifolia

1 reference

Rare biscoumarins and a chlorogenic acid derivative from Erycibe obtusifolia

Mandragora autumnalis

1 reference

Substances isolated from Mandragora species

Mandragora officinarum

2 references

Substances isolated from Mandragora species

New withanolides from Mandragora officinarum: first report of withanolides from the Genus Mandragora

Morus alba

3 references

Studies on the constituents of the leaves of Morus alba L.

Studies on the constituents of the leaves of Morus alba L.

Studies on the constituents of the leaves of Morus alba L.

Phellinus igniarius

3 references

Structures, Biogenesis, and Biological Activities of Pyrano[4,3-c]isochromen-4-one Derivatives from the FungusPhellinus igniarius

Structures, Biogenesis, and Biological Activities of Pyrano[4,3-c]isochromen-4-one Derivatives from the FungusPhellinus igniarius

Structures, Biogenesis, and Biological Activities of Pyrano[4, 3-c]isochromen-4-one Derivatives from the Fungus Phellinus igniarius

Aesculus hippocastanum

1 reference

Aesculus hippocastanum L.

Ailanthus triphysa

1 reference

Chemical Constituents of Ailanthus triphysa

Althaea armeniaca

1 reference

Coumarins of Althaea officinalis and A. armenica

Althaea officinalis

2 references

Coumarins of Althaea officinalis and A. armenica

Coumarins of Althaea officinalis and A. armenica

Angelica dahurica

1 reference

Coumarin glycosides from the roots ofAngelica dahurica

Artemisia alba

1 reference

Flavonol and Coumarin Glycosides from Artemisia incanescens

Artemisia capillaris

2 references

New constituents and antiplatelet aggregation and anti-HIV principles of Artemisia capillaris

New constituents and antiplatelet aggregation and anti-HIV principles of Artemisia capillaris

Artemisia iwayomogi

2 references

Chlorogenic acid, an antioxidant principle from the aerial parts ofArtemisia iwayomogi that acts on 1,1-diphenyl-2-picrylhydrazyl radical

Artemisia iwayomogi Extract Attenuates High-Fat Diet-Induced Obesity by Decreasing the Expression of Genes Associated with Adipogenesis in Mice

Artemisia vestita

1 reference

Mono- and sesquiterpenes and antifungal constituents from Artemisia species

Astragalus brachycarpus

1 reference

Phenolic compounds ofAstragalus brachycarpus. I

Astragalus onobrychis

1 reference

Coumarins and phenolic carboxylic acids from Astragalus onobrychis

Baccharis tricuneata

2 references

Cytotoxic activity of five compounds isolated from Colombian plants.

Cytotoxic constituents of Baccharis gaudichaudiana

Beaumontia grandiflora

1 reference

Chemical constituents of Duabanga grandiflora (Lythraceae)

Corchorus olitorius

1 reference

Medicinal foodstuffs. V. Moroheiya. (1): Absolute stereostructures of corchoionosides A, B, and C, histamine release inhibitors from the leaves of Vietnamese Corchorus olitorius L. (Tiliaceae)

Dendrobium densiflorum

1 reference

Dihydroayapin, a new coumarin compound from Dendrobium densiflorum

Diplolophium buchananii

2 references

Monoterpene, chromone and coumarin glucosides of Diplolophium buchananii

Monoterpene, chromone and coumarin glucosides of Diplolophium buchananii

Haplophyllum acutifolium

2 references

Coumarin glycosides ofHaplophyllum perforatum

Coumarin glycosides ofHaplophyllum perforatum

Helichrysum arenarium

2 references

Medicinal flowers. XXVII. New flavanone and chalcone glycosides, arenariumosides I, II, III, and IV, and tumor necrosis factor-alpha inhibitors from everlasting, flowers of Helichrysum arenarium

Medicinal flowers. XXX. Eight new glycosides, everlastosides F-M, from the flowers of Helichrysum arenarium

Hydrophyllum tenuipes

1 reference

BIOSYSTEMATICS OF THE GENUS HYDROPHYLLUM L. (HYDROPHYLLACEAE)

Hymenodictyon floribundum

1 reference

Glycoside derivatives of scopoletin and β-sitosterol from Hymenodictyon floribundum

Ipomoea digitata

1 reference

Chemical constituents from roots of Pueraria lobata

Machilus thunbergii

1 reference

A butanolide and phenolics from Machilus thunbergii

Manihot Esculenta

1 reference

Accumulation of Hydroxycoumarins During Post-harvest Deterioration of Tuberous Roots of Cassava (Manihot esculenta Crantz)

Murraya paniculata

5 references

Constituents of Flowers ofMurraya Paniculata

Coumarins of the flowers of Murraya paniculata

A flavonoid and indole alkaloid from flowers of Murraya paniculata

Murrayatin, a coumarin from murraya exotica

Coumarins of the flowers of Murraya paniculata

Neonauclea sessilifolia

2 references

Two chromone-secoiridoid glycosides and three indole alkaloid glycosides from Neonauclea sessilifolia

Two chromone-secoiridoid glycosides and three indole alkaloid glycosides from Neonauclea sessilifolia

Olea europaea

1 reference

Coumarin and secoiridoid glucosides from bark of Olea africana and Olea capensis.

Physochlaina physaloides

2 references

Coumarins of Physochlaina physaloides

Coumarins of Physochlaina physaloides

Achillea impatiens

1 reference

Coumarins ofPtarmica impatiens andP. ptarmicifolia

Santolina oblongifolia

1 reference

Antiinflammatory Activity of Coumarins fromSantolina oblongifolia

Falconeria insignis

2 references

Diterpene esters and phenolic compounds from Sapium insigne (ROYLE) BENTH. ex HOOK. fil.

Diterpene esters and phenolic compounds from Sapium insigne (ROYLE) BENTH. ex HOOK. fil.

Scaphopetalum thonneri

1 reference

Scaphopetalone and scaphopetalumate, a lignan and a triterpene ester from Scaphopetalum thonneri.

Sida hermaphrodita

2 references

Chemical study of Sida hermaphrodita

Chemical study of Sida hermaphrodita

Skimmia japonica

2 references

A Furanocoumarin glucoside from stembark of Skimmia japonica

A Furanocoumarin glucoside from stembark of Skimmia japonica

Viburnum suspensum

2 references

Iridoid glycosides from Viburnum suspensum

Iridoid glycosides from Viburnum suspensum

Catunaregam obovata

1 reference

A coumarin glucoside from xeromphis obovata

Catunaregam spinosa

1 reference

2D NMR Structure Elucidation of a New Coumarin Glycoside from Xeromphis spinosa

Artemisia ordosica

1 reference

Artemisioside, a new monoterpene glucoside from the aerial parts of Artemisia ordosica (Asteraceae).

Artemisia suksdorfii

1 reference

Alpha-pinene-type monoterpenes and other constituents from Artemisia suksdorfii

Cephalanthus occidentalis

1 reference

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

Echinacea purpurea

1 reference

Structure and accumulation of phenolics in elicited Echinacea purpurea cell cultures.

Eucalyptus viminalis

1 reference

Coumarins from Eucalyptus viminalis leaves

Eurycoma longifolia

1 reference

2,3-Dehydro-4α-hydroxylongilactone, a novel quassinoid and two known phenyl propanoids from Eurycoma longifolia Jack

Evolvulus alsinoides

1 reference

Anti-stress constituents of Evolvulus alsinoides: an ayurvedic crude drug.

Macaranga tanarius

1 reference

Absolute configuration of (+)-pinoresinol 4-O-[6''-O-galloyl]-beta-D-glucopyranoside, macarangiosides E, and F isolated from the leaves of Macaranga tanarius

Mentzelia albescens

1 reference

Iridoid mono- and di-glycosides in Mentzelia

Mentzelia arborescens

1 reference

Iridoid mono- and di-glycosides in Mentzelia

Ipomoea nil

1 reference

Umbelliferone released from hairy root cultures of Pharbitis nil treated with copper sulfate and its subsequent glucosylation.

Salsola laricifolia

1 reference

A chemical study of plants of the Mongolian flora lariside ? A new scopoletin glycoside fromSalsola laricifolia

Saussurea cordifolia

1 reference

Chemical constituents from Saussurea cordifolia

Saussurea hieracioides

1 reference

Chemical constituents of Saussurea superba

Saussurea superba

1 reference

Chemical constituents of Saussurea superba

Viburnum odoratissimum var. awabuki

1 reference

Chemical studies on Viburnum awabuki K. Koch.

Weigela subsessilis

1 reference

Inhibitory effect of coumarins from Weigela subsessilis on low density lipoprotein oxidation.

Artemisia dalai-lamae

1 reference

Chemical constituents of Artemisia lactiflora(Ⅱ)

peach

1 reference

Coumarins of Prunella vulgaris

Artemisia gmelinii

2 references

Chlorogenic acid, an antioxidant principle from the aerial parts ofArtemisia iwayomogi that acts on 1,1-diphenyl-2-picrylhydrazyl radical

Artemisia iwayomogi Extract Attenuates High-Fat Diet-Induced Obesity by Decreasing the Expression of Genes Associated with Adipogenesis in Mice

Hydrophyllum virginianum

1 reference

BIOSYSTEMATICS OF THE GENUS HYDROPHYLLUM L. (HYDROPHYLLACEAE)

Kitagawia praeruptora

1 reference

Structures of linear furano- and simple-coumarin glycosides of Bai-Hua Qian-Hu

Ripariosida hermaphrodita

1 reference

Chemical study of Sida hermaphrodita

Acer saccharum

1 reference

Phenolic glycosides from sugar maple (Acer saccharum) bark

0 references

0 references

0 references

Identifiers

InChI

InChI=1S/C16H18O9/c1-22-9-4-7-2-3-12(18)23-8(7)5-10(9)24-16-15(21)14(20)13(19)11(6-17)25-16/h2-5,11,13-17,19-21H,6H2,1H3/t11-,13-,14+,15-,16-/m1/s1

1 reference

SGTCGCCQZOUMJJ-YMILTQATSA-N

Scopolin (English)

4 October 2016

2 references

Scopolin (English)

4 October 2016

ChEBI release 2020-09-01

2 references

SGTCGCCQZOUMJJ-YMILTQATSA-N

scopolin (English)

4 October 2016

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=531-44-2

1 reference

Scopolin (English)

4 October 2016

1 reference

English

title

Scopolin (English)

retrieved

4 October 2016

Reaxys registry number

50851

1 reference

scopolin (English)

4 October 2016

mapping relation type

1 reference

scopolin (English)

4 October 2016

1 reference

splash10-0006-0900000000-ea1b1eba81851a071cea

SCOPOLIN (English)

4 October 2016

1 reference

0 references

DSSTox substance ID

DTXSID20967621

0 references

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

scopolin (English)

4 October 2016

1 reference

UNII

1Y49270PY8