(Q891785)

(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol

Syringin (English)

5 October 2016

1 reference

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol

inferred from InChIKey

2 references

2,6-Dimethoxy-4-(3-hydroxy-1-propenyl)phenyl beta-D-galactopyranoside

inferred from InChIKey

1 reference

1 reference

(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol

inferred from InChI

1 reference

(2S,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₁₇H₂₄O₉

1 reference

Syringin (English)

19 November 2016

COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO

1 reference

Syringin (English)

19 November 2016

COC1=CC(=CC(=C1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)OC)/C=C/CO

1 reference

Constituintes químicos isolados dos caules de Michelia champaca L. (Magnoliaceae)

Syringin (English)

19 November 2016

1 reference

Artemisia minor

2 references

Chemical constituents from the aerial parts of Artemisia minor.

Chemical Constituents of the Aerial Parts of Artemisia iwayomogi

Atractylodes lancea

6 references

Glycosides of Atractylodes ovata

Glycosides of Atractylodes ovata.

Studies on the constituents of Atractylodes lancea.

Glycosides of Atractylodes ovata

Studies on the Constituents of Atractylodes. II

Glycosides of Atractylodes ovata

Chrozophora plicata

4 references

Phenylpropanoid glucosides from Chrozophora obliqua

Phenylpropanoid glucosides from Chrozophora obliqua

Phenylpropanoid glucosides from Chrozophora obliqua

Phenylpropanoid glucosides from Chrozophora obliqua

Daphne feddei

4 references

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

Daphne oleoides

2 references

Terpenoids and aromatic compounds from Daphne oleoides ssp. oleoides

Phenylpropanoid Glycosides from Daphne oleoides.

Foeniculum vulgare

4 references

Phenolic glycosides from Foeniculum vulgare fruit and evaluation of antioxidative activity

Water-Soluble Constituents of Fennel. V. Glycosides of Aromatic Compounds.

Five New Monoterpene Glycosides and Other Compounds from Foeniculi Fructus (Fruit of Foeniculum vulgare MILLER).

Phenolic glycosides from Foeniculum vulgare fruit and evaluation of antioxidative activity

Gnidia polycephala

3 references

Phenylpropanoid glycosides of Gnidia polycephala

Phenylpropanoid glycosides of Gnidia polycephala

Phenylpropanoid glycosides of Gnidia polycephala

Jasminum lanceolarium

1 reference

Two new flavanone glycosides of Jasminum lanceolarium and their anti-oxidant activities

Jasminum nudiflorum

3 references

Nine new secoiridoid glucosides from Jasminum nudiflorum.

Nine new secoiridoid glucosides from Jasminum nudiflorum.

Nine new secoiridoid glucosides from Jasminum nudiflorum.

Linaria vulgaris

3 references

A new pyrroloquinazoline alkaloid from Linaria vulgaris

A new pyrroloquinazoline alkaloid from Linaria vulgaris

A new pyrroloquinazoline alkaloid from Linaria vulgaris

Prosopis juliflora

1 reference

Growth inhibitory alkaloids from mesquite (Prosopis juliflora (Sw.) DC.) leaves

Rafflesia kerrii

2 references

Hydrolyzable tannins and phenylpropanoid from Rafflesia kerrii Meijer (Rafflesiaceae)

Hydrolyzable tannins and phenylpropanoid from Rafflesia kerrii Meijer (Rafflesiaceae)

Stachys byzantina

3 references

Viscum album

11 references

Phenylpropanes and Lignans ofViscum albumCardioactive Drugs V1

Quality Control for RNA Preparations

Viscum album (European Mistletoe)

Studies on the vascular effects of the fractions and phenolic compounds isolated from Viscum album ssp. album

Pharmacological activity of phenylpropanoids of the mistletoe, Viscum album L., host: Pyrus caucasica Fed.

Phenylpropanes and Lignans ofViscum albumCardioactive Drugs V1

Two New Flavonoid Glycosides from Viscum album ssp. album

HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC DETERMINATION OF SYRINGIN IN VISCUM ALBUM L. SSP. ALBUM SAMPLES COLLECTED FROM DIFFERENT HOST PLANTS

THE COMPARATIVE STUDIES ON PHENYLPROPANOID GLYCOSIDES OF VISCUM ALBUM SUBSPECIES BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY

Studies on the constituents of the european mistletoe, Viscum album L.

Viscum album (mistletoe)

Phlomis aurea

3 references

Iridoid and megastigmane glycosides from Phlomis aurea

Iridoid and megastigmane glycosides from Phlomis aurea

Iridoid and megastigmane glycosides from Phlomis aurea

Ruellia patula

2 references

Three new flavonoid glycosides, byzantionoside B 6'-O-sulfate and xyloglucoside of (Z)-hex-3-en-1-ol from Ruellia patula

Three new flavonoid glycosides, byzantionoside B 6'-O-sulfate and xyloglucoside of (Z)-hex-3-en-1-ol from Ruellia patula

Ruellia tuberosa

1 reference

Chemical constituents from the leaves of Ruellia tuberosa

Sanchezia nobilis

1 reference

Cinnamyl Alcohol, Benzyl Alcohol, and Flavonoid Glycosides from Sanchezia nobilis

Sanchezia oblonga

1 reference

Cinnamyl Alcohol, Benzyl Alcohol, and Flavonoid Glycosides from Sanchezia nobilis

Adenophora stenanthina

1 reference

ChemInform Abstract: New Steroids from Adenophora stenanthina subsp. xifengensis.

Anethum graveolens

1 reference

Water-soluble constituents of dill

celery

1 reference

Polar constituents of celery seed

Picradeniopsis schaffneri

1 reference

The monoterpene 9-hydroxythymol from Bahia schaffneri var. aristata

Buddleja scordioides

1 reference

Triterpenoid saponins and other glycosides from Buddleja scordioides

Carthamus lanatus

1 reference

Bioactive Phenolics from Carthamus lanatus L.

Carthamus tinctorius

1 reference

6-hydroxykaempferol and its glycosides from Carthamus tinctorius petals

Carum carvi

1 reference

Water-soluble constituents of caraway: aromatic compound, aromatic compound glucoside and glucides

Psephellus bellus

1 reference

Syringin in some species of the subtribe Centaureinae of the Asteraceae

Psephellus simplicicaulis

1 reference

Syringin in some species of the subtribe Centaureinae of the Asteraceae

Chamaecyparis obtusa

1 reference

Structure and physiological activity of phenyl propanoid glycosides in the leaf of hinoki (Chamaecyparies obtusa Sieb. et Zucc.).

Cirsium arvense var. integrifolium

2 references

Chemical investigation ofCirsium setosum

Chemical investigation ofCirsium setosum

Cistanche mongolica

1 reference

The constituents of Cistanche tubulosa (Schrenk) Hook. f. II. Isolation and structures of a new phenylethanoid glycoside and a new neolignan glycoside.

Cistanche salsa

1 reference

Studies on the constituents of cistanchis herba. III. Isolation and structures of new phenylpropanoid glycosides, cistanosides A and B.

Codonopsis ussuriensis

1 reference

Isolation of triterpenoid and phenylpropanoid fromCodonopsis ussuriensis

Daphne acutiloba

2 references

Two biflavonoids from Daphne acutiloba

Two biflavonoids from Daphne acutiloba

Daphne arisanensis

2 references

A New Coumarin Glucoside from Daphne arisanensis.

A New Coumarin Glucoside from Daphne arisanensis.

Daphne genkwa

1 reference

[Chemical studies on the constituents of the thymelaeaceous plants. IV. Structure of a new spiro biflavonoid, genkwanol A, from the root of Daphne genkwa Sieb. et Zucc]

Putranjiva roxburghii

1 reference

Phenylpropanoid Glycosides and Tetrahydrofurofuranlignan Glycosides from the Adaptogenic Plant Drugs Tinospora cordifola and Drypetes roxburghii

Eleutherococcus koreanus

1 reference

Studies on the Constituents of Epimedium koreanum.

Eleutherococcus trifoliatus

1 reference

Two new phenylpropanoid glycosides from the stem bark of Acanthopanax trifoliatus

Euphorbia hirta

1 reference

Hirtionosides A-C, gallates of megastigmane glucosides, 3-hydroxyoctanoic acid glucosides and a phenylpropanoid glucoside from the whole plants of Euphorbia hirta.

Glehnia littoralis

2 references

New lignan glycosides from Glehnia littoralis

A new isoxazol from Glehnia littoralis

Helichrysum arenarium

3 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

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

Helogyne hutchisonii

1 reference

Sesquiterpene lactones from helogyne hutchisonii

Ilex chinensis

1 reference

Polar constituents of Mosla Chinensis

Ilex rotunda

1 reference

A dimeric sinapaldehyde glucoside from Ilex rotunda

Itoa orientalis

1 reference

Itosides J-N from Itoa orientalis and structure - anti-COX-2 activity relationship of phenolic glycosides

Jasminum mesnyi

1 reference

Four secoiridoid glucosides from Jasminum mesnyi

Kalopanax septemlobus

3 references

A potent anti-diabetic agent from Kalopanax pictus

Studies on the constituents of the bark of Kalopanax pictus Nakai.

Essential moiety for antimutagenic and cytotoxic activity of hederagenin monodesmosides and bisdesmosides isolated from the stem bark of Kalopanax pictus.

Ligusticum lucidum

1 reference

Chemical constituents from fruits of Ligustrum lucidum

Ligustrum obtusifolium

1 reference

Studies on the Constituents of Ligustrum Species. XIII. : Structures of Phenylethanoid Glycosides from the Leaves of Ligustrum obtusifolium SIEB. et ZUCC.

Linaria japonica

2 references

Iridoid glucosides from Linaria japonica

Iridoid glucosides from Linaria japonica

Linum flavum

1 reference

Lignans from L. flavum var. compactum (Linaceae)

Magnolia denudata

1 reference

Chemical constituents from the leaves of Magnolia denudata

Magnolia biondii

1 reference

Three new neolignans, fargesones A, B and C, from the flower buds of Magnolia fargesii.

Magnolia crassipes

1 reference

Phenolic constituents from Oplopanax horridus

Magnolia lacei

1 reference

Sesquiterpenoids from Saussurea laniceps and their chemotaxonomic significance

Osmanthus × fortunei

1 reference

Studies on the Constituents of Osmanthus Species. IV. On the Components of the Leaves of Osmanthus fortunei CARR.

Osmanthus ilicifolius

1 reference

Studies on the Constituents of Osmanthus Species. III. On the Components of the Leaves of Osmanthus ilicifolius (HASSK.) MOUILLEFERT

Oxytropis myriophylla

1 reference

Phenolic glucosides from Oxytropis myriophylla

Magnolia yunnanensis

1 reference

Chemical Constituents of Ainsliaea yunnanensis

Phellodendron amurense

2 references

Phenolic constituents of phellodendron amurense bark

Phenolic constituents of phellodendron amurense bark

Phillyrea latifolia

3 references

Lignan and phenylpropanoid glycosides from Phillyrea latifolia and their in vitro anti-inflammatory activity

Phytochemical analysis of Phillyrea latifolia L., a new source of oleuropeoside

Lignan and phenylpropanoid glycosides from Phillyrea latifolia and their in vitro anti-inflammatory activity

Picrasma quassioides

1 reference

Phenylpropanoids and other secondary metabolites from fresh fruits of Picrasma quassioides

Polygala chamaebuxus

1 reference

Glycosidic Constituents of some European Polygala Species

Prunus ssiori

1 reference

Two new lignan xylosides from the barks of Prunus ssiori and Prunus padus.

Salvadora persica

2 references

Lignan glycosides from stems of Salvadora persica

Lignan glycosides from stems of Salvadora persica

Saussurea controversa

1 reference

The chemical composition of the extractive substances ofSaussurea controversa

Saussurea medusa

4 references

Biologically active phenols from Saussurea medusa

Biologically active phenols from Saussurea medusa

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

Biologically Active Phenols from Saussurea medusa

Scutellaria orientalis

1 reference

Two phenethyl alcohol glycosides from Scutellaria orientalis subsp. pinnatifida

Scutellaria strigillosa

1 reference

Studies on the constituents of Scutellaria species (XXI): constituents of the leaves of Scutellaria strigillosa Hemsley

Sinapis arvensis

1 reference

Chemical and biological studies of Sinapis arvensis growing in Egypt

Stellera chamaejasme

4 references

Phenylpropanoid glycosides from Stellera chamaejasme

Biflavanones, diterpenes, and coumarins from the roots of Stellera chamaejasme L.

Biflavanones, diterpenes, and coumarins from the roots of Stellera chamaejasme L.

Phenylpropanoid glycosides from Stellera chamaejasme

Stevia gilliesii

1 reference

Guaianolides fromStevia gilliesii

Syringa josikaea

1 reference

TLC and HPLC analysis of syringin in Syringa vulgaris

Syringa vulgaris

4 references

Hypotensive action of syringin fromSyringa vulgaris

Phenolic compounds of the bark of Syringa vulgaris

TLC and HPLC analysis of syringin in Syringa vulgaris

TLC and HPLC analysis of syringin in Syringa vulgaris

common dandelion

1 reference

Further sesquiterpenoids and phenolics from Taraxacum officinale

Tinospora cordifolia

5 references

Cordioside, a clerodane furano diterpene glucoside from Tinospora cordifolia

Immunopotentiating compounds from Tinospora cordifolia

Phenylpropanoid Glycosides and Tetrahydrofurofuranlignan Glycosides from the Adaptogenic Plant Drugs Tinospora cordifola and Drypetes roxburghii

Aporphine alkaloids, clerodane diterpenes, and other constituents from Tinospora cordifolia

Cordioside, a clerodane furano diterpene glucoside from Tinospora cordifolia

Tinospora crispa

1 reference

Antioxidant and lipophilic constituents of Tinospora crispa

Tinospora hainanensis

2 references

A New N-Methyltetrahydroprotoberberine Alkaloid from Tinospora hainanensis.

A New N-Methyltetrahydroprotoberberine Alkaloid from Tinospora hainanensis.

Viscum coloratum

1 reference

Studies on the constituents of the Japanese mistletoe, Viscum album L. var. coloratum Ohwi grown on different host trees.

Wikstroemia sikokiana

3 references

Three biflavonoids from Wikstroemia sikokiana

Two new phenylpropanoid glycosides from Wikstroemia sikokiana.

Two new phenylpropanoid glycosides from Wikstroemia sikokiana.

Ficus microcarpa

1 reference

Antioxidant activity of a new C-glycosylflavone from the leaves of Ficus microcarpa

Acanthus ebracteatus

1 reference

Megastigmane, aliphatic alcohol and benzoxazinoid glycosides from Acanthus ebracteatus

Anagyris foetida

1 reference

Cytotoxic constituents from Anagyris foetida leaves

Carallia brachiata

1 reference

A new diglycosyl megastigmane from Carallia brachiata

Carex distachya

1 reference

Potential food additives from Carex distachya roots: identification and in vitro antioxidant properties

Centaurea deflexa

1 reference

Anti-proliferative activity of aguerin B and a new rare nor-guaianolide lactone isolated from the aerial parts of Centaurea deflexa

Clematis hexapetala

1 reference

Chemical Constituents From The Roots And Rhizomes Of Clematis Hexapetala Pall.

Codonopsis lanceolata

1 reference

Triterpene glycosides from the roots of Codonopsis lanceolata

Dracaena cambodiana

1 reference

New C27Steroidal Bisdesmosides from the Fresh Stems ofDracaena cambodiana

Globularia alypum

3 references

New Iridoid Glucosides and a Lignan Diglucoside fromGlobularia alypumL

Antioxidant constituents of the aerial parts of Globularia alypum growing in Morocco.

Phenylethyl Glycosides fromGlobularia alypumGrowing in Turkey

Osmanthus armatus

1 reference

Constituents from the heartwoods of Osmanthus armatus

Phellodendron chinense

1 reference

Phenolic constituents of Phellodendron chinense bark

Salacia chinensis

1 reference

Chemical structures and hepatoprotective effects of constituents from the leaves of Salacia chinensis

Saussurea cordifolia

1 reference

Chemical constituents from Saussurea cordifolia

Saussurea involucrata

1 reference

Chemical constituents from the cell cultures of Saussurea involucrata

Saussurea laniceps

1 reference

Two New Lignan Glycosides fromSaussurea laniceps

Saussurea triangulata

1 reference

A new sesquiterpene glycoside from the aerial parts of Saussurea triangulata

Taraxacum platycarpum

1 reference

Sesquiterpenoids and phenolics from Taraxacum hondoense.

Taraxacum udum

2 references

Sesquiterpenoids and phenolics from roots of Taraxacum udum.

Structural analysis of 1L-chiro-inositol diester from Taraxacum udum

Tetracentron sinense

1 reference

A new 8-O-4' neolignan glycoside from Tetracentron sinense

Tinospora sinensis

1 reference

A new dinorclerone diterpenoid glycoside from Tinospora sinensis

Torricellia angulata

1 reference

Iridoid glucosides in Griselinia, Aralidium and Toricellia

Vateria indica

1 reference

Chemical constituents in the leaves of Vateria indica

Zantedeschia aethiopica

1 reference

Antialgal compounds from zantedeschia aethiopica

Zanthoxylum schinifolium

1 reference

Cytotoxic Constituents from the Leaves of Zanthoxylum schinifolium

Glochidion zeylanicum

1 reference

Chemical constituents of the leaves of Glochidion obliquum and their bioactivity

Dolomiaea costus

3 references

Effects of sesquiterpenes and amino acid-sesquiterpene conjugates from the roots of Saussurea lappa on inducible nitric oxide synthase and heat shock protein in lipopolysaccharide-activated macrophages

Absolute Stereostructures and Syntheses of Saussureamines A, B, C, D and E, Amino Acid–Sesquiterpene Conjugates with Gastroprotective Effect, from the Roots of Saussurea lappa

Saussureamines A, B, C, D, and E, new anti-ulcer principles from Chinese Saussureae Radix.

Acer pictum

3 references

Studies on the constituents of the bark of Kalopanax pictus Nakai.

A potent anti-diabetic agent from Kalopanax pictus

Essential moiety for antimutagenic and cytotoxic activity of hederagenin monodesmosides and bisdesmosides isolated from the stem bark of Kalopanax pictus.

Styrax japonicus

1 reference

New furofuran and butyrolactone lignans with antioxidant activity from the stem bark of Styrax japonica

Magnolia obovata

2 references

Anti-platelet effect of the constituents isolated from the barks and fruits of Magnolia obovata

Effects of constituents from the bark of Magnolia obovata on nitric oxide production in lipopolysaccharide-activated macrophages

Magnolia sieboldii

1 reference

Syringin 4-O-beta-glucoside, a new phenylpropanoid glycoside, and costunolide, a nitric oxide synthase inhibitor, from the stem bark of Magnolia sieboldii.

Codonopsis pilosula

1 reference

Two New Triterpenoids from the Roots of Codonopsis pilosula.

Magnolia officinalis

1 reference

Cytotoxic lignans from the stem bark of Magnolia officinalis.

Syringa reticulata

1 reference

Secoiridoid glucosides and related compounds from Syringa reticulata and their antioxidant activities

Chrozophora obliqua

1 reference

Phenylpropanoid glucosides from Chrozophora obliqua

Eleutherococcus sessiliflorus

1 reference

Authentication of the traditional medicinal plant Eleutherococcus senticosus by DNA and chemical analyses

rooibos

1 reference

Safety Assessment of Phytochemicals Derived from the Globalized South African Rooibos Tea (Aspalathus linearis) through Interaction with CYP, PXR, and Pgp

Osmanthus heterophyllus

1 reference

Studies on the Constituents of Osmanthus Species. III. On the Components of the Leaves of Osmanthus ilicifolius (HASSK.) MOUILLEFERT

Eleutherococcus senticosus

18 references

Studies on the Constituents of Epimedium koreanum.

An improved extraction procedure for the rapid, quantitative high-performance liquid chromatographic estimation of the main eleutherosides (b and e) inEleutherococcus senticosus (eleuthero)

Effects of various Eleutherococcus senticosus cortex on swimming time, natural killer activity and corticosterone level in forced swimming stressed mice

Investigation of the pharmacokinetics and mechanism of action of glycosides ofEleuterococcus. I. Introduction of tritium into eleuteroside B. kinetics of its accumulation and elimination from the animal organism

A benzenoid from the stem of Acanthopanax senticosus

A new lignan glycoside from Eleutherococcus senticosus

Phenolic compounds of Eleutherococcus senticosus

Phenolic compounds of the bark of Eleutherococcus senticosus

Search for naturally occurring substances to prevent the complications of diabetes. II. Inhibitory effect of coumarin and flavonoid derivatives on bovine lens aldose reductase and rabbit platelet aggregation

NMR STUDY OF MU-AGATOXIN

Immunopharmacological in vitro effects of Eleutherococcus senticosus extracts

Induction of apoptosis by Acanthopanax senticosus HARMS and its component, sesamin in human stomach cancer KATO III cells

Phenolic compounds from stem bark of Acanthopanax senticosus and their pharmacological effect in chronic swimming stressed rats

The isolation ofeleutherococcus senticosus constituents by centrifugal partition chromatography and their quantitative determination by high performance liquid chromatography

Micellar electrokinetic chromatographic/ultraviolet diode array analysis ofEleutherococcus senticosus

HPLC method for preliminary analysis of constituents in rat blood after oral administration of the extract of Acanthopanax senticosus.

Authentication of the traditional medicinal plant Eleutherococcus senticosus by DNA and chemical analyses

Pharmacokinetics and mechanism of action ofEleutherococcus glycosides. VII. Influence of an extract and individual glycosides on protein biosynthesis

Stachys palaestina

1 reference

Alpinia zerumbet

1 reference

Several Steroids and Phenylpropanoid Glycosides isolated from Leaves of Getto (Alpinia speciosa K. Schum.)

Boraginaceae

1 reference

Chemical constituents of Lythospermum fruticosum

Etlingera elatior

1 reference

Several Steroids and Phenylpropanoid Glycosides isolated from Leaves of Getto (Alpinia speciosa K. Schum.)

Lithodora fruticosa

1 reference

Chemical constituents of Lythospermum fruticosum

described by source

Ottův slovník naučný

statement is subject of

Q106297045

0 references

Commons category

Syringin

0 references

Identifiers

InChI

InChI=1S/C17H24O9/c1-23-10-6-9(4-3-5-18)7-11(24-2)16(10)26-17-15(22)14(21)13(20)12(8-19)25-17/h3-4,6-7,12-15,17-22H,5,8H2,1-2H3/b4-3+/t12-,13-,14+,15-,17+/m1/s1

1 reference

QJVXKWHHAMZTBY-GCPOEHJPSA-N

Syringin (English)

19 November 2016

2 references

Syringin (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

118-34-3

2 references

Global Substance Registration System

UNII

I6F5B11C96

English

eleutheroside b (English)

QJVXKWHHAMZTBY-GCPOEHJPSA-N

19 November 2016

InChIKey

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=118-34-3

1 reference

Syringin (English)

5 October 2016

1 reference

English

Syringin (English)

19 November 2016

Reaxys registry number

97166

1 reference

syringin (English)

5 October 2016

mapping relation type

1 reference

SYRINGIN (English)

19 November 2016

1 reference

MSBNK-Univ_Toyama-TY000098

SYRINGIN (English)

19 November 2016

1 reference

MassBank accession ID

0 references

SPLASH

splash10-00di-9000000000-fa802a2a89fb979b26fe

0 references

splash10-03di-0900000000-6d7b6ef12dba764fc7fd

0 references

DSSTox substance ID

DTXSID2042438

1 reference

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

DSSTOX compound identifier

0 references

0 references

601-519-0

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.120.487

27 December 2018

ECHA Substance Infocard ID

(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-{4-[(1E)-3-hydroxyprop-1-en-1-yl]-2,6-dimethoxyphenoxy}oxane-3,4,5-triol (English)

quotation

CAS no.: 118-34-3 (English)

100.120.487

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.120.487

27 December 2018

PesticideInfo chemical ID

(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-{4-[(1E)-3-hydroxyprop-1-en-1-yl]-2,6-dimethoxyphenoxy}oxane-3,4,5-triol (English)

quotation

CAS no.: 118-34-3 (English)

0 references

1 reference

1 reference

syringin (English)

5 October 2016

1 reference

syringin (English)

5 October 2016

1 reference

Global Substance Registration System

syringin (English)

5 October 2016

1 reference

UNII

I6F5B11C96

English

eleutheroside b (English)

19 November 2016

0 references

1 reference

syringin (English)

5 October 2016

1 reference