(Q23418564)

inferred from SMILES

mass

624.169±0 dalton

1 reference

Narcissoside (English)

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-4H-chromen-3-yl 6-O-(6-deoxy-alpha-D-mannopyranosyl)-beta-D-glucopyranoside

14 October 2016

stereoisomer of

2 references

inferred from InChIKey

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

2 references

inferred from InChIKey

isorhamnetin 3-robinobioside

1 reference

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

2-(3-Methoxy-4-hydroxyphenyl)-3-[6-O-(beta-L-rhamnopyranosyl)-beta-D-glucopyranosyloxy]-5,7-dihydroxy-4H-1-benzopyran-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

Narcissoside, >=95% (HPLC)

1 reference

chemical formula

C₂₈H₃₂O₁₆

1 reference

Narcissoside (English)

14 October 2016

canonical SMILES

CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O

1 reference

Narcissoside (English)

14 October 2016

isomeric SMILES

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O

1 reference

Phylogenetic relationship of six Glycyrrhiza species based on rbcL sequences and chemical constituents.

Narcissoside (English)

14 October 2016

1 reference

Astragalus levieri

1 reference

Flavonoids ofAstragalus levieri andA. sevangensis

Astragalus sevangensis

1 reference

Flavonoids ofAstragalus levieri andA. sevangensis

Strumpfia maritima

1 reference

Biological and phytochemical investigation of plants XVI: Strumpfia maritima (Rubiaceae)

Daniellia oliveri

1 reference

Phytochemical and antimicrobial activities of the Daniellia oliveri leaves

Aerva lanata

2 references

A study of the herb Aerva lanata IV. Flavonoid glycosides

Carbohydrates of Aerva lanata

Mercurialis annua

1 reference

Phytochemical investigation on Mercurialis annua

Astragalus dasyanthus

1 reference

Narcissin from Astragalus dasyanthus

Berchemia racemosa

1 reference

Constituents of Berchemia racemosa Sieb. et Zucc

Bupleurum longeradiatum

1 reference

Phenolic compounds of the roots ofBupleurum longeradiatum

Calendula officinalis

4 references

Flavonoids of inflorescences of Calendula officinalis

Anti-inflammatory, anti-tumor-promoting, and cytotoxic activities of constituents of marigold (Calendula officinalis) flowers

Flavonoids from Calendula officinalis flowers

Anti-inflammatory, anti-tumor-promoting, and cytotoxic activities of constituents of marigold (Calendula officinalis) flowers

Caragana aurantiaca

2 references

Flavonoids ofCaragana aurantiaca

Flavonoids ofCaragana aurantiaca

Caragana pygmaea

1 reference

Flavonoids ofCaragana pygmaea

Caragana spinosa

2 references

Flavonoids ofCaragana spinosa

Chemical investigation of Caragana spinosa runners

Dysphania procera

1 reference

Antifungal constituents of Chenopodium procerum

Citrus unshiu

2 references

Structure and Hypotensive Effect of Flavonoid Glycosides inCitrus unshiuPeelings

Studies on physiologically active substances in citrus peel. Part II. Structure and hypotensive effect of flavonoid glycosides in Citrus unshiu peelings.

Coleogyne ramosissima

3 references

Flavonoid and benzophenone glycosides from Coleogyne ramosissima

Anti-tumor promoting activity of polyphenols from Cowania mexicana and Coleogyne ramosissima.

Flavonoid and benzophenone glycosides from Coleogyne ramosissima

Hypericum ascyron

1 reference

Flavonoids of Hypericum ascyron

Morinda citrifolia

5 references

Chemical constituents of the fruits of Morinda citrifolia (Noni) and their antioxidant activity.

Chemical Constituents of the Fruits of Morinda citrifolia (Noni) and Their Antioxidant Activity

Chemical constituents of the fruits of Morinda citrifolia (Noni) and their antioxidant activity.

Chemical Constituents of the Fruits of Morinda citrifolia (Noni) and Their Antioxidant Activity

Chemical Constituents of the Fruits of Morinda citrifolia (Noni) and Their Antioxidant Activity

Onobrychis arenaria

3 references

Flavonoids of the epigeal part ofOnobrychis arenaria

Flavonoids from the aerial parts of Satureja khuzestanica

Flavonoids of the epigeal part ofOnobrychis arenaria

Peucedanum morisonii

1 reference

Flavonoids of Peucedanum morissonii

Potentilla erecta

1 reference

Flavonoids of Potentilla erecta

Salsola collina

1 reference

Flavonoids of Salsola collina

Salvadora persica

1 reference

FLAVONOID GLYCOSIDES FROM THE LEAVES OF SALVADORA PERSICA L.

Scolymus hispanicus

1 reference

Flavonol glycosides from Scolymus hispanicus and Jasonia glutinosa

Aster koraiensis

2 references

Chemical constituents from the aerial parts of Aster koraiensis with protein glycation and aldose reductase inhibitory activities

Chemical constituents from the aerial parts of Aster koraiensis with protein glycation and aldose reductase inhibitory activities

Kandelia candel

1 reference

Chemical constituents from Kandelia candel with their inhibitory effects on pro-inflammatory cytokines production in LPS-stimulated bone marrow-derived dendritic cells (BMDCs).

Marrubium velutinum

2 references

Identification of tyrosinase inhibitors from Marrubium velutinum and Marrubium cylleneum

Acylated flavonoid and phenylethanoid glycosides from Marrubium velutinum

Salsola oppositifolia

1 reference

In vitro cytotoxic activity of Salsola oppositifolia Desf. (Amaranthaceae) in a panel of tumour cell lines.

Nelumbo nucifera

1 reference

Simultaneous analysis of anthocyanin and non-anthocyanin flavonoid in various tissues of different lotus (Nelumbo) cultivars by HPLC-DAD-ESI-MS(n)

Achillea roseo-alba

1 reference

Flavonoid Glycosides from Achillea roseo-albax

Alhagi maurorum

1 reference

Flavonoids and anthocyans from Alhagi pseudoalhagi

Aristolochia kaempferi

1 reference

Constituents from the stem and root of Aristolochia kaempferi

Artemisia sublessingiana

1 reference

Flavonoids ofArtemisia sublessingiana

Astragalus icmadophilus

1 reference

Triterpene glycosides from Astragalus icmadophilus.

Barbarea vulgaris

1 reference

Flavonoid glycosides of Barbarea vulgaris L. (Brassicaceae)

Bellis perennis

1 reference

Medicinal flowers. XXI. Structures of perennisaponins A, B, C, D, E, and F, acylated oleanane-type triterpene oligoglycosides, from the flowers of Bellis perennis

Bupleurum rotundifolium

1 reference

Flavonoids ofBupleurum rotundifolium

Castanea sativa

1 reference

Inhaltsstoffe von Cupuliferae, II Ein neues acyliertes Flavonoidglykosid ausCastanea sativa Mill.

Ginkgo biloba

1 reference

Coumaroyl flavonol glycosides from the leaves of Ginkgo biloba

Goodyera schlechtendaliana

1 reference

Flavonoids from Goodyera schlechtendaliana

Halimodendron halodendron

1 reference

Preparative separation of phenolic compounds from Halimodendron halodendron by high-speed counter-current chromatography.

Halostachys caspica

1 reference

Flavonoids from Halostachys caspica and their antimicrobial and antioxidant activities.

Kaempferia parviflora

1 reference

Phenolic glycosides from Kaempferia parviflora

Lilium auratum

2 references

The Flavonolglycoside from Lilium Pollen

Narcissin (Isorhamnetin-3-rutinosid) aus den Pollen vonLilium auratum Lindle

Melicope micrococca

1 reference

Two novel prenylated flavones from the aerial parts of Melicope micrococca

Melilotus sulcatus

1 reference

Reactive Oxygen Species Scavenging Activity of Flavone Glycosides from Melilotus neapolitana

Narcissus tazetta

1 reference

Narcisin, a New Glucocide from the Flowers of Narcissus Tazetta L.

Onobrychis viciifolia

1 reference

Phenolic glycosides of forage legume Onobrychis viciifolia

Phoenix canariensis

1 reference

Studies on the Constituents of Palmae Plants. VI. Steroid Saponins and Flavonoids of Leaves of Phoenix canariensis hort. ex CHABAUD, P. humilis ROYLE var. hanceana BECC., P. dactylifera L., and Licuala spinosa WURMB.

Picea abies

1 reference

Syringetin 3-O-(6″-acetyl)-β-glucopyranoside and other flavonols from needles of norway spruce, Picea abies

Planchonella obovata

1 reference

Three New Benzophenone Glucosides from the Leaves ofPlanchonella obovata

Podocarpus fasciculus

1 reference

Cytotoxic constituents from Podocarpus fasciculus

Prunus amygdalus

1 reference

Antioxidative phenolic compounds isolated from almond skins (Prunus amygdalus Batsch).

Prunus dulcis

1 reference

Antioxidative phenolic compounds isolated from almond skins (Prunus amygdalus Batsch).

Prunus cerasus

2 references

Antioxidant properties of sour cherries (Prunus cerasus L.): role of colorless phytochemicals from the methanolic extract of ripe fruits

Antioxidant polyphenols from tart cherries (Prunus cerasus).

Kali turgida

1 reference

Cytotoxic extracts of Salsola oppositifolia Desf. (Amaranthaceae) against non-small lung carcinoma (CORL-23) and melanoma (C32) cells

Salsola kali

1 reference

Cytotoxic extracts of Salsola oppositifolia Desf. (Amaranthaceae) against non-small lung carcinoma (CORL-23) and melanoma (C32) cells

Saussurea medusa

1 reference

Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa

Styphnolobium japonicum

1 reference

The selected flavonol glycoside derived from Sophorae Flos improves glucose uptake and inhibits adipocyte differentiation via activation AMPK in 3T3-L1 cells

Halostachys belangeriana

1 reference

Flavonoids from Halostachys caspica and their antimicrobial and antioxidant activities.

Bryobium erioides

1 reference

Phenolic glycosides from Kaempferia parviflora

Kali turgidum

1 reference

Cytotoxic extracts of Salsola oppositifolia Desf. (Amaranthaceae) against non-small lung carcinoma (CORL-23) and melanoma (C32) cells

Isotrema kaempferi

1 reference

Constituents from the stem and root of Aristolochia kaempferi

Astragalus aegobromus

1 reference

Flavonoids ofAstragalus torrentum

Bryobium eriaeoides

1 reference

Phenolic glycosides from Kaempferia parviflora

Gomphocarpus sinaicus

1 reference

Flavonoid glycosides from Egyptian species of the tribe Asclepiadeae (Apocynaceae, subfamily Asclepiadoideae)

Atractylis carduus

1 reference

Flavonoid glycosides and triterpenoids from Atractylis flava

Nitraria retusa

1 reference

Flavonol glycosides from Nitraria retusa

Foeniculum vulgare

1 reference

Separation and characterization of phenolic compounds in fennel (Foeniculum vulgare) using liquid chromatography-negative electrospray ionization tandem mass spectrometry.

Opuntia ficus-indica

1 reference

Phenolic composition, antioxidant and anti-inflammatory activities of extracts from Moroccan Opuntia ficus-indica flowers obtained by different extraction methods

Berchemia floribunda

1 reference

Constituents of Berchemia racemosa Sieb. et Zucc

mandarin orange

2 references

Structure and Hypotensive Effect of Flavonoid Glycosides inCitrus unshiuPeelings

Studies on physiologically active substances in citrus peel. Part II. Structure and hypotensive effect of flavonoid glycosides in Citrus unshiu peelings.

Citrus × deliciosa

2 references

Structure and Hypotensive Effect of Flavonoid Glycosides inCitrus unshiuPeelings

Studies on physiologically active substances in citrus peel. Part II. Structure and hypotensive effect of flavonoid glycosides in Citrus unshiu peelings.

Laennecia filaginoides

1 reference

Antiprotozoal activity of the constituents of Conyza filaginoides

Prunus avium

1 reference

Antioxidative phenolic compounds isolated from almond skins (Prunus amygdalus Batsch).

Astragalus varius

1 reference

Flavonoids of Astragalus virgatus

Anvillea garcinii

1 reference

Flavonoids of Anvillea garcini

Identifiers

InChI

InChI=1S/C28H32O16/c1-9-18(32)21(35)23(37)27(41-9)40-8-16-19(33)22(36)24(38)28(43-16)44-26-20(34)17-13(31)6-11(29)7-15(17)42-25(26)10-3-4-12(30)14(5-10)39-2/h3-7,9,16,18-19,21-24,27-33,35-38H,8H2,1-2H3/t9-,16+,18-,19+,21+,22-,23+,24+,27+,28-/m0/s1

1 reference

Narcissoside (English)

UIDGLYUNOUKLBM-GEBJFKNCSA-N

14 October 2016

InChIKey

1 reference

Global Substance Registration System

Narcissoside (English)

14 October 2016

2 references

UNII

N4AX11L1TF

UIDGLYUNOUKLBM-GEBJFKNCSA-N

narcissin (English)

14 October 2016

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=604-80-8

1 reference

Ramnazin-3-O-rutinoside (English)

14 October 2016

1 reference

Narcissoside (English)

14 October 2016

ChEBI ID

145096

mapping relation type

exact match

1 reference

ChEBI release 2021-03-01

1 reference

splash10-00di-0047009000-b6a0e3bb3d909325be14

NARCISSIN (English)

14 October 2016

1 reference

MassBank accession ID

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splash10-014i-0009000000-c8bb1df6ed921312f08d

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splash10-014i-0009000000-ef0b892b0615ecb7dea2

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splash10-000t-0006009000-1981f949656714e13c57

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splash10-014i-0009000000-e09efd0a7cc87ad1ebf2

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splash10-0002-0001009000-eee5f78d574441bd2f91

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splash10-014i-1009000000-0f5aa70db457047e0231

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splash10-00xr-0059005000-3565c9d1511c8ab964f3

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splash10-02t9-0009000000-bf026e576028dd19e8af

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splash10-004i-0000009000-0078dc6d944d4daee118

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splash10-016r-0009603000-86614d096c20119e0d32

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splash10-014i-0109000000-e7d80d986472dc942254

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splash10-014i-1009000000-d8db82d2b7b04799b388

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splash10-014i-3009000000-fe4abf9856da827009c0

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splash10-014i-2009000000-7b495dfbab26022e966f

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splash10-00di-0000009000-5ab122f2929f730763ff

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splash10-00di-0000009000-38b9b9dffd40a833720e

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splash10-00di-0000009000-4eebffcfe0425009d7da

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splash10-00xr-0007009000-0f8cc59d59869b38e2fd

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splash10-044i-0009002000-b3c581980efd416b63be

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splash10-02t9-0019000000-a7100702e850b6789ce7

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splash10-004i-0000009000-e42d07d75af0ca130aa4

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splash10-014i-0009402000-266f0ff78895d2a2cace

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splash10-014i-0109000000-03ac02b01cedb2035fdb

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splash10-014i-0009000000-f98391f228e2fbb4cb5d

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splash10-014i-2009000000-69d947e7a11b9f607373

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splash10-014i-4009000000-1a64a725a3532ba883fe

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splash10-00di-0000009000-8fdd9de8cf39de4d0814

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splash10-00di-0000009000-d84c9b2c28581253ea7c

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splash10-00di-0000009000-11ec08d763295e232c1a

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splash10-00di-0007009000-1641a082a8d7875698a9

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splash10-02t9-0009002000-faf2f0f4d55d80cce480

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splash10-03xr-0019000000-9592eb581eaa13359691

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splash10-014i-1009000000-86e4d3378d300b36c5a8

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splash10-00xr-0049006000-a8411529b6d691776adc

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splash10-014i-0009000000-a7104a79f9f0afdd646d

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splash10-0v4i-0449000000-edee83221343cce610bb

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splash10-01b9-0009004000-959e7249bce51effcd19

0 references

splash10-014i-0009000000-2c977d19dd292eaa4291

0 references

DSSTox substance ID

DTXSID00209157

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

UNII

N4AX11L1TF