Swertisin (Q82979547)

6-beta-D-Glucopyranosyl-4',5-dihydroxy-7-methoxyflavone

inferred from SMILES

1 reference

inferred from SMILES

mass

446.121296904 dalton

1 reference

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

inferred from SMILES

stereoisomer of

2 references

inferred from InChIKey

inferred from InChI

chemical formula

C₂₂H₂₂O₁₀

0 references

canonical SMILES

O=C1C=C(OC=2C=C(OC)C(=C(O)C12)C3OC(CO)C(O)C(O)C3O)C=4C=CC(O)=CC4

0 references

isomeric SMILES

COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O

0 references

found in taxon

Carex fraseriana

1 reference

Taxonomic implications of the flavonoids of Cymophyllus fraseri (Cyperaceae)

Passiflora incarnata

6 references

Separation of flavone C-glycosides and qualitative analysis of Passiflora incarnata L. by capillary zone electrophoresis

Mass spectrometric characterization of flavonoids in extracts from Passiflora incarnata

Isoscoparin-2″-O-glucoside from Passiflora incarnata

Quantification of the flavonoid glycosides in Passiflora incarnata by capillary electrophoresis

Isolation and Characterization of an Unknown Flavonoid in Dry Extracts fromPassiflora incarnata

Qualitative and quantitative reversed-phase high-performance liquid chromatography of flavonoids in Passiflora incarnata L.

Aleurites moluccanus

3 references

Isolation of a C-Glycoside Flavonoid with Antinociceptive Action from Aleurites moluccana Leaves

Separation of C-glycoside flavonoids from Aleurites moluccana using chitin and full N-acetylated chitin.

Aleurites moluccana (L.) Willd. Leaves: Mechanical Antinociceptive Properties of a Standardized Dried Extract and Its Chemical Markers

Aquilegia oxysepala

1 reference

[Studies on flavonoids from Cirsium setosum].

Cephalaria coriacea

1 reference

Cephalaria gigantea

1 reference

Fagraea blumei

1 reference

Iridoid Glucosides with Free Radical Scavenging Properties fromFagraea blumei

Fagraea obovata

1 reference

A new glycosyl flavone from Fagraea obovata wall

Galipea trifoliata

1 reference

C-glycosylflavones from Galipea trifoliata

Gentiana algida

1 reference

Xanthones and flavonoids of Gentiana algida and G. karelinii

Great yellow gentian

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentiana orbicularis

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianella austriaca

1 reference

Radioprotective effects of Gentianella austriaca fractions and polyphenolic constituents in human lymphocytes.

Gentianella campestris

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianella serotina

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis barbata

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis barbellata

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis ciliata

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis crinita

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis detonsa

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis grandis

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis lanceolata

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis paludosa

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis paludosa var. ovatodeltoidea

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis simplex

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gentianopsis thermalis

1 reference

Chemotaxonomy of Gentianopsis: Xanthones, C-glycosylflavonoids and carbohydrates

Gnetum gnemon

1 reference

C-Glycosylflavones in Gnetum gnemon

Iris x germanica

2 references

STUDIES ON THE CONSTITUENTS OF TWO IRIS SPECIES

Studies on the constituents of Iris florentina L. II. C-Glucosides of xanthones and flavones from the leaves.

Justicia pectoralis

1 reference

O-Methoxylated C-glycosylflavones from Justicia pectoralis

Knautia montana

1 reference

Knautia tatarica

1 reference

Passiflora biflora

1 reference

o-and c-glycosylflavones from passiflora biflora

Pterocephalus plumosus

1 reference

Saccharum officinarum

1 reference

New Flavonoids from Sugarcane (Saccharum)

Scabiosa atropurpurea

1 reference

Lomelosia olgae

1 reference

Swertia japonica

6 references

Studies on the mutagenicity of Swertiae Herba. I. Identification of the mutagenic components.

Studies on the constituents of swertia japonica: Isolation and structure of new flavonoids, swertisin and swertiajaponin.

Ueber die chemischen Bestandteile der japanischen Droge “To-Yaku” (Herba Swertiae, Ph. Jap. IV). I.

Qualitative and quantitative analysis of Swertia herbs by high performance liquid chromatography-diode array detector-mass spectrometry (HPLC-DAD-MS).

Über einen neuen Bestandteil von Swertia japonica, Makino (Gentianaceae)

Antihepatotoxic principles of Garcinia kola seeds

Swertia mussotii

1 reference

Two New Xanthone Glucosides from Swertia mussotii Franch

Swertia paniculata

1 reference

Chemical constituents of Swertia paniculata

Swertia tetrapetala

1 reference

[Studies on the constituents of medicinal plants in Hokkaido. II. On the whole herb of Frasera tetrapetala Pall. (2)]

Triticum aestivum

1 reference

Mechanism of antimutagenicity of wheat sprout extracts.

Wilbrandia ebracteata

2 references

Analysis of the plant drug Wilbrandia ebracteata (Cogn.) Cogn.

Potential insulin secretagogue effects of isovitexin and swertisin isolated from Wilbrandia ebracteata roots in non-diabetic rats

Syzygium cumini

1 reference

α-Glucosidase inhibitory hydrolyzable tannins from Eugenia jambolana seeds

Lophatherum gracile

1 reference

Simultaneous Determination of 10 Bioactive Components of Lophatherum gracile Brongn by HPLC-DAD

Machaerium hirtum

1 reference

Chemical constituents of Machaerium hirtum Vell. (Fabaceae) leaves and branches and its anti-inflammatory activity evaluation

Alliaria petiolata

1 reference

Isolation, Structure Elucidation, and Biological Activity of Flavone 6-C-Glycosides from Alliaria petiolata

Gaillardia aristata

1 reference

Pseudoguaianolides from Gaillardia aristata

Gaillardia pulchella

1 reference

Flavone-C-glycosides in a coastal race of Gaillardia pulchella

Swertia pseudochinensis

1 reference

Qualitative and quantitative analysis of Swertia herbs by high performance liquid chromatography-diode array detector-mass spectrometry (HPLC-DAD-MS).

Ziziphus jujuba

1 reference

Flavonoids from Ziziphus jujuba Mill var. spinosa

Myrcia splendens

1 reference

α-Glucosidase inhibitory hydrolyzable tannins from Eugenia jambolana seeds

Justicia canbyi

1 reference

Flavonoid chemistry of Siphonoglossa

Justicia ramosa

1 reference

Flavonoid chemistry of Siphonoglossa

Aquarius grandiflorus

2 references

Trans-Aconitic acid, glucosylflavones and hydroxycinnamoyltartaric acids from the leaves of Echinodorus grandiflorus ssp. aureus, a Brazilian medicinal plant

In Vitro TNF-α Inhibition Elicited by Extracts from Echinodorus grandiflorus Leaves and Correlation with Their Phytochemical Composition.

Livistona australis

1 reference

A sulphated flavone glycoside from Livistona australis and its antioxidant and cytotoxic activity

Identifiers

InChI

InChI=1S/C22H22O10/c1-30-13-7-14-16(11(25)6-12(31-14)9-2-4-10(24)5-3-9)19(27)17(13)22-21(29)20(28)18(26)15(8-23)32-22/h2-7,15,18,20-24,26-29H,8H2,1H3/t15-,18-,20+,21-,22+/m1/s1

0 references

0 references

CAS Registry Number

6991-10-2

1 reference

https://commonchemistry.cas.org/detail?cas_rn=6991-10-2

9 April 2021

PubChem CID

124034

1 reference

ChEBI ID

131838

mapping relation type

exact match

2 references

ChEBI release 2021-03-01

International Chemical Identifier

InChI

InChI=1S/C22H22O10/c1-30-13-7-14-16(11(25)6-12(31-14)9-2-4-10(24)5-3-9)19(27)17(13)22-21(29)20(28)18(26)15(8-23)32-22/h2-7,15,18,20-24,26-29H,8H2,1H3/t15-,18-,20+,21-,22+/m1/s1

SureChEMBL ID

SCHEMBL2778665

2 references

inferred from InChIKey

1 reference

1 reference

DSSTOX compound identifier

0 references

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

retrieved

15 January 2022