(Q27145412)

Isoschaftoside (English)

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one

8 October 2016

stereoisomer of

2 references

inferred from InChIKey

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one

2 references

inferred from InChIKey

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one

2 references

inferred from InChIKey

8-C-glucopyranosyl-6-C-xylopyranosylapigenin

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2R,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one

1 reference

1 reference

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one

1 reference

chemical formula

C₂₆H₂₈O₁₄

1 reference

Isoschaftoside (English)

8 October 2016

canonical SMILES

C1C(C(C(C(O1)C2=C(C3=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)OC(=CC3=O)C5=CC=C(C=C5)O)O)O)O)O

1 reference

Isoschaftoside (English)

8 October 2016

isomeric SMILES

C1[C@@H]([C@@H]([C@H]([C@@H](O1)C2=C(C3=C(C(=C2O)[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)OC(=CC3=O)C5=CC=C(C=C5)O)O)O)O)O

1 reference

Quantification of the flavonoid glycosides in Passiflora incarnata by capillary electrophoresis

Isoschaftoside (English)

8 October 2016

7 references

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Mass spectrometric characterization of flavonoids in extracts from Passiflora incarnata

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

Mass spectral characterization of C-glycosidic flavonoids isolated from a medicinal plant (Passiflora incarnata)

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

Isoscoparin-2″-O-glucoside from Passiflora incarnata

Notobasis syriaca

1 reference

FLAVONOIDS FROM PULICARIA ARABICA (L.) CASS.

Phoradendron tomentosum

1 reference

Flavone C-glycosides of Phoradendron tomentosum from different host trees

Passiflora allantophylla

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Passiflora ampullacea

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Passiflora boenderi

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Passiflora caerulea

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Passiflora colinvauxii

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Passiflora macrophylla

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Passiflora misera

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Passiflora pinnatistipula

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Passiflora serratifolia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Passiflora trisecta

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Ficus carica

1 reference

Isomeric Di-C-glycosylflavones in Fig (Ficus carica L.)

Haplopappus scrobiculatus

1 reference

Flavonoids of Haplopappus scrobiculatus and Haplopappus sericeus

Polypodium vulgare

1 reference

A new cyanogenic glycoside from Hordeum vulgare

Polypodium virginianum

1 reference

A new cyanogenic glycoside from Hordeum vulgare

Saccharum officinarum

2 references

New Flavonoids from Sugarcane (Saccharum)

Analysis of sugarcane flavonoids by capillary zone electrophoresis

Yeatesia viridiflora

1 reference

C-Glycosylflavones from Yeatesia viridiflora

Passiflora foetida

1 reference

C-Glycosylflavonoids From Passiflora foetida var. hispida and P. foetida var. hibiscifolia

Ceratonia siliqua

1 reference

C-glycosylflavones from Ceratonia siliqua cotyledons

Vitex lucens

1 reference

Bioactivity of extracts and isolated compounds from Vitex polygama (Verbenaceae) and Siphoneugena densiflora (Myrtaceae) against Spodoptera frugiperda (Lepidoptera: Noctuidae).

Vitex polygama

2 references

Bioactivity of extracts and isolated compounds from Vitex polygama (Verbenaceae) and Siphoneugena densiflora (Myrtaceae) against Spodoptera frugiperda (Lepidoptera: Noctuidae).

Compounds from Vitex polygama active against kidney diseases.

Artemisia judaica

2 references

Flavonoids of Artemisia judaica, A. Monosperma and A. herba-alba

Flavonoids of Artemisia judaica, A. Monosperma and A. herba-alba

Cotula cinerea

2 references

Flavonoids of Cotula cinerea

Flavonoids of Cotula cinerea

Achillea millefolium

1 reference

Leaf and flower head flavonoids of Achillea millefolium L. subspecies

Achillea nobilis

1 reference

Flavonoids from Achillea nobilis L.

Artemisia frigida

1 reference

Flavonoids from Artemisia frigida

Baccharis gaudichaudiana

1 reference

A New ent-Clerodane Diterpene from the Aerial Parts of Baccharis gaudichaudiana.

Camellia sinensis

3 references

Glycosidic flavonoids as rat-liver injury preventing compounds from green tea

Bioactive saponins and glycosides. XXVIII. New triterpene saponins, foliatheasaponins I, II, III, IV, and V, from Tencha (the leaves of Camellia sinensis).

Bioactive saponins and glycosides. XXV. Acylated oleanane-type triterpene saponins from the seeds of tea plant (Camellia sinensis)

Centaurea virgata

1 reference

6-Methoxylated and C-glycosyl flavonoids from Centaurea species

Galipea trifoliata

1 reference

C-glycosylflavones from Galipea trifoliata

Iris domestica

2 references

C-glycosyl compounds in the leaves of Gemmingia chinensis O. KUNTZE.

C-Glycosyl Compounds in the Leaves ofGemmingia chinensisO. Kuntze

Glycine max

2 references

C-glycosylflavones from roots of glycine max

C-glycosylflavones from roots of glycine max

liquorice

1 reference

Flavonoid constituents from Glycyrrhiza glabra hairy root cultures

Lespedeza davurica

1 reference

Flavonoid glycosides from fiveCyathea species

Ertela trifolia

1 reference

C-Glycosylflavones from Monnieria trifolia

Passiflora pittieri

1 reference

C-Glycosylflavonoids From Passiflora pittieri, P. alata, P., ambigua and Adenia mannii

Passiflora sexflora

1 reference

The Flavonoids of Passiflora sexflora

Ruscus aculeatus

1 reference

Flavonoids from the Aboveground Parts of Lycopus virginicus

Scorodocarpus borneensis

1 reference

Megastigmanes and flavonoids from the leaves of Scorodocarpus borneensis

Sphaerostephanos polycarpus

1 reference

Flavonoids from the Pinnae of Sphaerostephanos (Thelypteridaceae)

Triticum aestivum

1 reference

A new flavone O-glycoside and other constituents from wheat leaves (Triticum aestivum L.).

Achillea collina

1 reference

Flavonoids in Achillea collina

Desmodium styracifolium

1 reference

Flavonoid compounds from Desmodium styracifolium of Vietnamese origin

Desmodium sandwicense

1 reference

Isoschaftoside, a C-glycosylflavonoid from Desmodium uncinatum root exudate, is an allelochemical against the development of Striga.

Desmodium uncinatum

1 reference

Isoschaftoside, a C-glycosylflavonoid from Desmodium uncinatum root exudate, is an allelochemical against the development of Striga.

Gratiola officinalis

1 reference

8-Hydroxylated flavone O-glycosides and other flavonoids in chemotypes of Gratiola officinalis

Lespedeza capitata

1 reference

Isocarlinoside, a di-C-glycosylflavone from Lespedeza capitata

Scleropyrum pentandrum

1 reference

Unprecedented furan-2-carbonyl C-glycosides and phenolic diglycosides from Scleropyrum pentandrum

Scutellaria baicalensis

1 reference

Flavone di-C-glycosides from Scutellaria baicalensis

Viola yedoensis

1 reference

Flavone C-Glycosides from Viola yedoensis MAKINO

Grona styracifolia

1 reference

Flavonoid compounds from Desmodium styracifolium of Vietnamese origin

Cotula cinereum

1 reference

Flavonoids of Cotula cinerea

Vergonis planta

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – I. Application to Passiflora Flavonoids

Artemisia herba-alba

2 references

Flavonoid glycosides of Artemisia monosperma and A. herba-alba

Flavonoids of Artemisia judaica, A. Monosperma and A. herba-alba

Identifiers

InChI

InChI=1S/C26H28O14/c27-6-13-18(32)21(35)23(37)26(40-13)16-20(34)15(25-22(36)17(31)11(30)7-38-25)19(33)14-10(29)5-12(39-24(14)16)8-1-3-9(28)4-2-8/h1-5,11,13,17-18,21-23,25-28,30-37H,6-7H2/t11-,13+,17-,18+,21-,22+,23+,25-,26-/m0/s1

1 reference

Isoschaftoside (English)

OVMFOVNOXASTPA-VYUBKLCTSA-N

8 October 2016

InChIKey

2 references

Isoschaftoside (English)

8 October 2016

ChEBI release 2020-09-01

2 references

isoschaftoside (English)

OVMFOVNOXASTPA-VYUBKLCTSA-N

8 October 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=52012-29-0

1 reference

iso-Schaftoside (English)

8 October 2016

1 reference

Isoschaftoside (English)

8 October 2016

Reaxys registry number

1445782

1 reference

isoschaftoside (English)

8 October 2016

ChEBI ID

75589

mapping relation type

1 reference

isoschaftoside (English)

8 October 2016

1 reference

splash10-00mk-0000490000-d03b975a7c63dd249bf0

ISOSCHAFTOSIDE (English)

8 October 2016

1 reference

MassBank accession ID

MSBNK-Fiocruz-FIO00718

0 references

MSBNK-Fiocruz-FIO00719

0 references

MSBNK-Fiocruz-FIO00720

0 references

MSBNK-Fiocruz-FIO00721

0 references

MSBNK-Fiocruz-FIO00722

0 references

MSBNK-Fiocruz-FIO00723

0 references

MSBNK-Fiocruz-FIO00724

0 references

MSBNK-Fiocruz-FIO00725

0 references

MSBNK-Fiocruz-FIO00726

0 references

MSBNK-Fiocruz-FIO00727

0 references

SPLASH

0 references

splash10-056r-0003930000-19dcb29d2368b3e25e41

0 references

splash10-056r-0009600000-0dd49843a8c6d6c26683

0 references

splash10-004j-0019100000-1bab41f6c87d1446d28f

0 references

splash10-03di-0000090000-122343e9c226bc8442bb

0 references

splash10-03di-0000090000-912d27419fb8670bfef7

0 references

splash10-03di-0000190000-62300971ae35f106a878

0 references

splash10-0w30-0009770000-8cdd765a2fa621e832cb

0 references

splash10-0ue9-0009100000-c753093417a9b812fe57

0 references

splash10-0udi-0009520000-010be1f9d059e9f29780

0 references

UNII

H27X8715V3

1 reference

Global Substance Registration System

UNII

H27X8715V3