(Q358968)

English

coniferin

chemical compound

Coniferyl alcohol beta-D-glucoside
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxy-phenoxy]tetrahydropyran-3,4,5-triol
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxy-phenoxy]oxane-3,4,5-triol
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]oxane-3,4,5-triol
(2S,3R,4S,5S,6R)-2-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxy-phenoxy]-6-methylol-tetrahydropyran-3,4,5-triol
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]tetrahydropyran-3,4,5-triol

In more languages

Statements

type of chemical entity

0 references

chemical compound

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coniferin metabolic process

subject has role

1 reference

Gene Ontology release 2020-05-02

coniferyl-alcohol glucosyltransferase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

coniferin beta-glucosidase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

Coniferin structure.svg
620 × 245; 18 KB

1 reference

imported from Wikimedia project

German Wikipedia

342.131468 dalton

1 reference

language of work or name

Coniferin (English)

4 October 2016

stereoisomer of

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₆H₂₂O₈

1 reference

language of work or name

Coniferin (English)

4 October 2016

canonical SMILES

COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O

1 reference

language of work or name

Coniferin (English)

4 October 2016

isomeric SMILES

COC1=C(C=CC(=C1)/C=C/CO)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O

1 reference

language of work or name

Coniferin (English)

4 October 2016

Mutisia acerosa

1 reference

Sesquiterpenes and other constituents from chilean mutisieae

2 references

Characterisation of Phenolic Constituents from Juvenile and Mature Needles of Norway Spruce by Means of High Performance Liquid Chromatography-Mass Spectrometry

Preparative separation of phenolic compounds from Picea abies by high-speed counter-current chromatography

Cynomorium songaricum

2 references

Inhibitory effects of ursolic acid derivatives from Cynomorium songaricum, and related triterpenes on human immunodeficiency viral protease

Inhibitory effects of constituents from Cynomorium songaricum and related triterpene derivatives on HIV-1 protease

Balanophora abbreviata

3 references

A new lignan from Balanophora abbreviata and inhibition of lipopolysaccharide (LPS)-induced inducible nitric oxide synthase (iNOS) expression

A New Lignan (I) from Balanophora abbreviata and Inhibition of Lipopolysaccharide (LPS)-Induced Inducible Nitric Oxide Synthase (iNOS) Expression.

A new lignan from Balanophora abbreviata and inhibition of lipopolysaccharide (LPS)-induced inducible nitric oxide synthase (iNOS) expression

Rhodiola crenulata

2 references

Bioactive constituents from Chinese natural medicines. XXVIII. Chemical structures of acyclic alcohol glycosides from the roots of Rhodiola crenulata

Bioactive constituents from Chinese natural medicines. XXVIII. Chemical structures of acyclic alcohol glycosides from the roots of Rhodiola crenulata

Stachys byzantina

2 references

Iridoid glycoside constituents of Stachys lanata

Iridoid glycoside constituents of Stachys lanata

Angelica archangelica

1 reference

Dihydrofurocoumarin glucosides from Angelica archangelica and Angelica silvestris

Artemisia stolonifera

1 reference

Phenolic constituents from the aerial parts ofArtemisia stolonifera

Balanophora fungosa

2 references

Galloyl and hexahydroxydiphenoyl esters of phenylpropanoid glucosides, phenylpropanoids and phenylpropanoid glucosides from rhizome of Balanophora fungosa

Melanin synthesis inhibitors from Balanophora fungosa

Callitris drummondii

1 reference

The biotechnological production of podophyllotoxin and related cytotoxic lignans by plant cell cultures

1 reference

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

Chamaecyparis obtusa

1 reference

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

Daphne oleoides

2 references

Phenylpropanoid Glycosides from Daphne oleoides.

Phenylpropanoid Glycosides from Daphne oleoides.

Eleutherococcus koreanus

1 reference

Studies on the chemical constituents ofAcanthopanax koreanum (II)

Itoa orientalis

2 references

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

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

Kalopanax septemlobus

1 reference

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

Ligustrum ovalifolium

1 reference

Biosynthesis of secoiridoid glucosides in oleaceae

Cardiocrinum cordatum

2 references

Flavonol and phenylpropanoid glycosides from Lilium cordatum

Flavonol and phenylpropanoid glycosides from Lilium cordatum

6 references

Aryltetralin lignans from Linum flavum and Linum capitatum

Lignans from L. flavum var. compactum (Linaceae)

The Accumulation of Coniferin in, and its Isolation from, a High-Producing Cell Suspension ofLinum flavum

On the podophyllotoxins of root cultures of Linum flavum

Aryltetralin lignans from Linum flavum and Linum capitatum

Formation of beta-peltatin-A methyl ether and coniferin by root cultures of Linum flavum.

Nardostachys jatamansi

1 reference

11-Methoxyviburtinal, a new iridoid from Valeriana jatamansi

Valeriana jatamansi

2 references

11-Methoxyviburtinal, a new iridoid from Valeriana jatamansi

11-Methoxyviburtinal, a new iridoid from Valeriana jatamansi

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

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 crenata

1 reference

Quassinoids and Other Constituents from Picrasma crenata

Polygala chamaebuxus

1 reference

Glycosidic Constituents of some European Polygala Species

Syringa vulgaris

3 references

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

Thujopsis dolabrata

1 reference

Terpenoid- and Phenyl Propanoid-Glycosides Isolated from Leaves of Hiba (Thujopsis dolabrata SEIB. et ZUCC.).

4 references

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.

Two New Flavonoid Glycosides from Viscum album ssp. album

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

Astragalus bungeanus

1 reference

Coniferyl alcohol glucoside from Astragalus bungeanus

Balanophora harlandii

1 reference

A New Hydrolyzable Tannin fromBalanophora harlandiiwith Radical-Scavenging Activity

Balanophora japonica

1 reference

Balanophonin, a new neo-lignan from Balanophora japonica Makino.

Balanophora laxiflora

1 reference

Phenolic constituents from Balanophora laxiflora with DPPH radical-scavenging activity.

2 references

Sinalexin, a phytoalexin from white mustard elicited by destruxin B and Alternaria brassicae

Phytoalexins and polar metabolites from the oilseeds canola and rapeseed: differential metabolic responses to the biotroph Albugo candida and to abiotic stress

Camellia crassicolumna

1 reference

Phenolic antioxidants from green tea produced from Camellia crassicolumna Var. multiplex

Camellia crassicolumna var. multiplex

1 reference

Phenolic antioxidants from green tea produced from Camellia crassicolumna Var. multiplex

Codonopsis cordifolioidea

2 references

Phenylpropanoids from the Roots of Codonopsis cordifolioidea and Their Biological Activities

Three New Polyyne (=Polyacetylene) Glucosides from the Edible Roots ofCodonopsis cordifolioidea

Echinacea purpurea

1 reference

Structure and accumulation of phenolics in elicited Echinacea purpurea cell cultures

1 reference

Accumulation of podophyllotoxin and related lignans in cell suspension cultures of linum album

Osmanthus armatus

1 reference

Constituents from the heartwoods of Osmanthus armatus

1 reference

Comparison of phenolic compounds from galls and shoots of Picea glauca

Picrorhiza scrophulariiflora

1 reference

Phenyl and Phenylethyl Glycosides fromPicrorhiza scrophulariiflora

Prunus domestica

1 reference

A new bipyrrole and some phenolic constituents in prunes (Prunus domestica L.) and their oxygen radical absorbance capacity (ORAC).

Salacia chinensis

1 reference

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

Zantedeschia aethiopica

1 reference

Antialgal compounds from zantedeschia aethiopica

Gentiana straminea

1 reference

Traceability of Geographical Origin in Gentiana straminea by UPLC-Q Exactive Mass and Multivariate Analyses

Neopicrorhiza scrophulariiflora

1 reference

Phenyl and Phenylethyl Glycosides fromPicrorhiza scrophulariiflora

Artemisia argyi

1 reference

Phenolic constituents from the aerial parts ofArtemisia stolonifera

1 reference

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

Astragalus onobrychis

1 reference

Coniferyl alcohol glucoside from Astragalus bungeanus

Citrus × paradisi

1 reference

Coniferin—an astringent glycoside in citrus

1 reference

New isoflavone glycosides from Iris spuria L. (Calizona) cultivated in Egypt.

mandarin orange

1 reference

Discrimination of Citrus reticulata Blanco and Citrus reticulata 'Chachi' as well as the Citrus reticulata 'Chachi' within different storage years using ultra high performance liquid chromatography quadrupole/time-of-flight mass spectrometry based m

1 reference

Biochemical characterization of the suberization-associated anionic peroxidase of potato

Valeriana officinalis

1 reference

Water soluble chemical constituents of Valeriana officinalis Linn. var. latiofolia Miq.

Osmanthus heterophyllus

1 reference

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

Citrus × deliciosa

1 reference

Discrimination of Citrus reticulata Blanco and Citrus reticulata 'Chachi' as well as the Citrus reticulata 'Chachi' within different storage years using ultra high performance liquid chromatography quadrupole/time-of-flight mass spectrometry based m

Eleutherococcus senticosus

4 references

Studies on the chemical constituents ofAcanthopanax koreanum (II)

Phenolic compounds of Eleutherococcus senticosus

Phenolic compounds of the bark of Eleutherococcus senticosus

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

Stachys palaestina

1 reference

Iridoid glycoside constituents of Stachys lanata

Alpinia zerumbet

1 reference

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

Etlingera elatior

1 reference

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

described by source

Meyers Konversations-Lexikon, 4th edition (1885–1890)

statement is subject of

0 references

Ottův slovník naučný

statement is subject of

0 references

Identifiers

InChI=1S/C16H22O8/c1-22-11-7-9(3-2-6-17)4-5-10(11)23-16-15(21)14(20)13(19)12(8-18)24-16/h2-5,7,12-21H,6,8H2,1H3/b3-2+/t12-,13-,14+,15-,16-/m1/s1

1 reference

language of work or name

Coniferin (English)

4 October 2016

SFLMUHDGSQZDOW-FAOXUISGSA-N

2 references

language of work or name

Coniferin (English)

4 October 2016

ChEBI release 2020-09-01

CAS Registry Number

1 reference

language of work or name

coniferin (English)

4 October 2016

1 reference

language of work or name

Abietin (English)

4 October 2016

1 reference

language of work or name

Coniferin (English)

4 October 2016

Reaxys registry number

1296933

1 reference

language of work or name

coniferin (English)

4 October 2016

mapping relation type

2 references

language of work or name

coniferin (English)

4 October 2016

matched by identifier from

International Chemical Identifier

InChI=1S/C16H22O8/c1-22-11-7-9(3-2-6-17)4-5-10(11)23-16-15(21)14(20)13(19)12(8-18)24-16/h2-5,7,12-21H,6,8H2,1H3/b3-2+/t12-,13-,14+,15-,16-/m1/s1

1 reference

language of work or name

CONIFERIN (English)

4 October 2016

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

SFLMUHDGSQZDOW-FAOXUISGSA-N

UniChem compound ID

1 reference

splash10-014i-0019000000-010d6745a3773ac224bb

0 references

803-885-9

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

[No public or meaningful name is available] (English)

CAS no.: 531-29-3 (English)

ECHA Substance Infocard ID

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

[No public or meaningful name is available] (English)

CAS no.: 531-29-3 (English)

Cannabis Database ID

1 reference

Cannabis Database

Human Metabolome Database ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

SFLMUHDGSQZDOW-FAOXUISGSA-N

1 reference

language of work or name

coniferin (English)

4 October 2016

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

SFLMUHDGSQZDOW-FAOXUISGSA-N

2 references

Global Substance Registration System

language of work or name

CONIFERIN (English)

4 October 2016

matched by identifier from

SFLMUHDGSQZDOW-FAOXUISGSA-N

Probes And Drugs ID

0 references

0 references

1 reference

Freebase Data Dumps

publication date

28 October 2013

Gran Enciclopèdia Catalana ID

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Gran Enciclopèdia Catalana ID (former scheme)

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Microsoft Academic ID

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Römpp online ID

1 reference

imported from Wikimedia project

German Wikipedia

Store norske leksikon ID

0 references

Sitelinks

Wikipedia(11 entries)

cswiki Koniferin
dewiki Coniferin
enwiki Coniferin
eowiki Koniferino
eswiki Coniferin
frwiki Coniférine
jawiki コニフェリン
ptwiki Coniferina
shwiki Koniferin
srwiki Koniferin
svwiki Koniferin

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)

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