(Q104667296)

English

scopolin

No description defined

In more languages

default for all languages

No label defined

No description defined

edit

Statements

instance of

type of chemical entity

0 references

subclass of

chemical compound

0 references

mass

356.11073222 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₁₆H₂₀O₉

0 references

canonical SMILES

O=C1OC2=CC(OC3OC(CO)C(O)C(O)C3O)=C(OC)C=C2CC1

0 references

isomeric SMILES

COc1cc2c(cc1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)OC(=O)CC2

0 references

found in taxon

Inulanthera nuda

1 reference

stated in

Phenols, Acetylenes, and Sesquiterpene Lactones fromInulanthera nuda

Aesculus pavia

1 reference

stated in

Cytotoxic triterpenoid saponins from the fruits of Aesculus pavia L.

Artemisia minor

1 reference

stated in

Chemical constituents from the aerial parts of Artemisia minor.

Baptisia arachnifera

1 reference

stated in

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia bracteata

1 reference

stated in

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia calycosa

1 reference

stated in

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia cinerea

1 reference

stated in

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia lanceolata

1 reference

stated in

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia nuttalliana

1 reference

stated in

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia perfoliata

1 reference

stated in

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia simplicifolia

1 reference

stated in

Distribution of flavonoids in the genus baptisia (leguminosae)

Baptisia tinctoria

1 reference

stated in

Distribution of flavonoids in the genus baptisia (leguminosae)

Erycibe obtusifolia

1 reference

stated in

Rare biscoumarins and a chlorogenic acid derivative from Erycibe obtusifolia

Mandragora autumnalis

1 reference

stated in

Substances isolated from Mandragora species

Mandragora officinarum

1 reference

stated in

Substances isolated from Mandragora species

Morus alba

2 references

stated in

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

stated in

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

Phellinus igniarius

2 references

stated in

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

stated in

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

Ailanthus triphysa

1 reference

stated in

Chemical Constituents of Ailanthus triphysa

Althaea armeniaca

1 reference

stated in

Coumarins of Althaea officinalis and A. armenica

Althaea officinalis

1 reference

stated in

Coumarins of Althaea officinalis and A. armenica

Angelica dahurica

1 reference

stated in

Coumarin glycosides from the roots ofAngelica dahurica

Artemisia alba

1 reference

stated in

Flavonol and Coumarin Glycosides from Artemisia incanescens

Artemisia capillaris

1 reference

stated in

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

Artemisia iwayomogi

2 references

stated in

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

stated in

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

Artemisia vestita

1 reference

stated in

Mono- and sesquiterpenes and antifungal constituents from Artemisia species

Astragalus onobrychis

1 reference

stated in

Coumarins and phenolic carboxylic acids from Astragalus onobrychis

Baccharis tricuneata

1 reference

stated in

Cytotoxic activity of five compounds isolated from Colombian plants.

Corchorus olitorius

1 reference

stated in

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

stated in

Dihydroayapin, a new coumarin compound from Dendrobium densiflorum

Diplolophium buchananii

1 reference

stated in

Monoterpene, chromone and coumarin glucosides of Diplolophium buchananii

Haplophyllum acutifolium

1 reference

stated in

Coumarin glycosides ofHaplophyllum perforatum

Helichrysum arenarium

1 reference

stated in

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

Hydrophyllum tenuipes

1 reference

stated in

BIOSYSTEMATICS OF THE GENUS HYDROPHYLLUM L. (HYDROPHYLLACEAE)

Hymenodictyon floribundum

1 reference

stated in

Glycoside derivatives of scopoletin and β-sitosterol from Hymenodictyon floribundum

Machilus thunbergii

1 reference

stated in

A butanolide and phenolics from Machilus thunbergii

Manihot Esculenta

1 reference

stated in

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

Murraya paniculata

3 references

stated in

A flavonoid and indole alkaloid from flowers of Murraya paniculata

stated in

Constituents of Flowers ofMurraya Paniculata

stated in

Coumarins of the flowers of Murraya paniculata

Neonauclea sessilifolia

1 reference

stated in

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

Olea europaea

1 reference

stated in

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

Kitagawia praeruptora

1 reference

stated in

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

Physochlaina physaloides

1 reference

stated in

Coumarins of Physochlaina physaloides

Achillea biserrata

2 references

stated in

Components ofPtarmica bisserata

stated in

Coumarins ofPtarmica bisserata

Achillea impatiens

1 reference

stated in

Coumarins ofPtarmica impatiens andP. ptarmicifolia

Santolina oblongifolia

1 reference

stated in

Antiinflammatory Activity of Coumarins fromSantolina oblongifolia

Falconeria insignis

1 reference

stated in

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

Scaphopetalum thonneri

1 reference

stated in

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

Sida hermaphrodita

1 reference

stated in

Chemical study of Sida hermaphrodita

Skimmia japonica

1 reference

stated in

A Furanocoumarin glucoside from stembark of Skimmia japonica

Viburnum suspensum

1 reference

stated in

Iridoid glycosides from Viburnum suspensum

Catunaregam obovata

1 reference

stated in

A coumarin glucoside from xeromphis obovata

Catunaregam spinosa

1 reference

stated in

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

Arabidopsis thaliana

1 reference

stated in

AtMetExpress development: a phytochemical atlas of Arabidopsis development

Prunus persica

1 reference

stated in

Coumarins of Prunella vulgaris

Salsola laricifolia

1 reference

stated in

Chemical study of plants of the Mongolian flora coumarins of Salsola laricifolia

Artemisia gmelinii

2 references

stated in

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

stated in

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

Hydrophyllum virginianum

1 reference

stated in

BIOSYSTEMATICS OF THE GENUS HYDROPHYLLUM L. (HYDROPHYLLACEAE)

Ripariosida hermaphrodita

1 reference

stated in

Chemical study of Sida hermaphrodita

Simaroubaceae

1 reference

stated in

Two quassinoid glycosides and a β-carboline-1-propionic acid from hannoa klaineana

Identifiers

InChI

InChI=1S/C16H20O9/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/h4-5,11,13-17,19-21H,2-3,6H2,1H3/t11-,13-,14+,15-,16-/m1/s1

0 references

InChIKey

WSHSQJSPOLYHLM-YMILTQATSA-N

0 references

2 references

26 December 2021

matched by identifier from

InChIKey

WSHSQJSPOLYHLM-YMILTQATSA-N

1 reference

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q104667296&oldid=2156564334"