(E)-coniferyl alcohol (Q418993)

coniferyl-alcohol glucosyltransferase activity

part of

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

coniferyl-alcohol dehydrogenase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

Coniferol.svg
620 × 213; 10 KB

1 reference

imported from Wikimedia project

German Wikipedia

mass

180.079 dalton

1 reference

CONIFERYL ALCOHOL (English)

19 October 2016

chemical formula

C₁₀H₁₂O₃

1 reference

CONIFERYL ALCOHOL (English)

19 November 2016

canonical SMILES

COC1=C(C=CC(=C1)C=CCO)O

1 reference

CONIFERYL ALCOHOL (English)

19 November 2016

isomeric SMILES

COC1=C(C=CC(=C1)/C=C/CO)O

1 reference

CONIFERYL ALCOHOL (English)

19 November 2016

melting point

76 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Xanthium spinosum

1 reference

Xanthanolides from Xanthium: Absolute configuration of xanthanol, isoxanthanol and their C-4 epimers

Paecilomyces fulvus

2 references

Microbial synthesis of coniferyl alcohol by the fungus Byssochlamys fulva V107

Microbial synthesis of coniferyl alcohol by the fungus Byssochlamys fulva V107

Pinus strobus

1 reference

Suppression of CCR impacts metabolite profile and cell wall composition in Pinus radiata tracheary elements

Hedyotis lawsoniae

1 reference

Studies on the constituents of medicinal and related plants in Sri Lanka. III. Novel sesquilignans from Hedyotis lawsoniae.

Helicteres angustifolia

2 references

Pregnane, coumarin and lupane derivatives and cytotoxic constituents from Helicteres angustifolia

Pregnane, coumarin and lupane derivatives and cytotoxic constituents from Helicteres angustifolia

Stemona collinsae

2 references

Antifungal stilbenoids from Stemona collinsae.

Antifungal stilbenoids from Stemona collinsae.

Artemisia alba

1 reference

Flavonol and Coumarin Glycosides from Artemisia incanescens

Codonopsis pilosula

1 reference

New Constituents from Codonopsis pilosula

Coleogyne ramosissima

1 reference

Flavonoid and benzophenone glycosides from Coleogyne ramosissima

Bactrocera dorsalis

1 reference

Accumulation of phenylpropanoids in the rectal glands of males of the Oriental fruit fly,Dacus dorsalis

Eleutherococcus senticosus

1 reference

Phenolic compounds of Eleutherococcus senticosus

Tabernaemontana divaricata

1 reference

Capillary Gas Chromatographic Analysis of Indole Alkaloids: Investigation of the Indole Alkaloids Present in Tabernaemontana divaricata Cell Suspension Culture

Fagus grandifolia

2 references

Cis-monolignols in Fagus grandifolia and their possible involvement in lignification

Cis-monolignols in Fagus grandifolia and their possible involvement in lignification

Hibiscus taiwanensis

1 reference

Constituents from the Stems of Hibiscus taiwanensis.

Linum flavum

3 references

Aryltetralin lignans from Linum flavum and Linum capitatum

Lignans from L. flavum var. compactum (Linaceae)

Aryltetralin lignans from Linum flavum and Linum capitatum

Machilus thunbergii

1 reference

A butanolide and phenolics from Machilus thunbergii

Picea abies

2 references

Phenolic extractives from root bark of Picea abies

Analysis of chemical changes in Picea abies wood decayed by different Streptomyces strains showing evidence for biopulping procedures

Pinus sylvestris

1 reference

Monoaryl and cyclohexenone glycosides from needles of Pinus sylvestris

Pinus taeda

1 reference

Multi-Site Modulation of Flux during Monolignol Formation in Loblolly Pine (Pinus taeda)

Pisum sativum

1 reference

Identification of Plant Factors Inducing Virulence Gene Expression in Agrobacterium tumefaciens.

Populus tremuloides

1 reference

Bud exudate composition of Populus tremuloides

Saccharum officinarum

1 reference

Antioxidative Compounds Isolated from Kokuto, Non-centrifugal Cane Sugar

Securidaca longepedunculata

1 reference

Gas chromatographic/mass spectrometric investigation of the volatile main components from roots ofSecuridaca longipedunculata

Asparagus cochinchinensis

2 references

Bioactive constituents from Asparagus cochinchinensis.

Bioactive constituents from Asparagus cochinchinensis.

Morus australis

1 reference

In vitro anti-diabetic activity and chemical characterization of an apolar fraction of Morus alba leaf water extract.

Morus bombycis

1 reference

In vitro anti-diabetic activity and chemical characterization of an apolar fraction of Morus alba leaf water extract.

Artemisia xerophytica

1 reference

Sesquiterpene lactones and other constituents from Artemisia xerophytica

Broussonetia papyrifera

1 reference

Antioxidant phenolics from Broussonetia papyrifera fruits

Echinacea purpurea

1 reference

Structure and accumulation of phenolics in elicited Echinacea purpurea cell cultures

Linum album

1 reference

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

Magnolia officinalis

1 reference

Phenolic constituents from the stem bark of Magnolia officinalis

Daucus carota

1 reference

Biosynthesis of methyleugenol and methylisoeugenol in Daucus carota leaves: Characterization of eugenol/isoeugenol synthase and O-Methyltransferase

Morus indica

1 reference

In vitro anti-diabetic activity and chemical characterization of an apolar fraction of Morus alba leaf water extract.

Morus alba

1 reference

In vitro anti-diabetic activity and chemical characterization of an apolar fraction of Morus alba leaf water extract.

Aeschynanthus bracteatus

1 reference

Chemical constituents of Aeschynanthus bracteatus and their weak anti-inflammatory activities.

Mangifera indica

1 reference

Glycosidically-bound aroma volatile compounds in the skin and pulp of ‘Kensington Pride’ mango fruit at different stages of maturity

potato

2 references

Metabolite profiling of red and blue potatoes revealed cultivar and tissue specific patterns for anthocyanins and other polyphenols.

Biochemical characterization of the suberization-associated anionic peroxidase of potato

Arabidopsis thaliana

1 reference

Identification of primary and secondary metabolites with phosphorus status-dependent abundance inArabidopsis, and of the transcription factor PHR1 as a major regulator of metabolic changes during phosphorus limitation

Boraginaceae

1 reference

Chemical constituents of Lythospermum fruticosum

Lithodora fruticosa

1 reference

Chemical constituents of Lythospermum fruticosum

described by source

Brockhaus and Efron Encyclopedic Dictionary

statement is subject of

Q24445599

0 references

Commons category

Coniferyl alcohol

0 references

Identifiers

InChI

InChI=1S/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3/b3-2+

1 reference

CONIFERYL ALCOHOL (English)

19 November 2016

2 references

CONIFERYL ALCOHOL (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

32811-40-8

1 reference

https://commonchemistry.cas.org/detail?cas_rn=32811-40-8

10 April 2021

1 reference

Coniferol (English)

19 November 2016

2 references

CONIFERYL ALCOHOL (English)

19 November 2016

Reaxys registry number

2048963

1 reference

coniferol (English)

19 October 2016

mapping relation type

2 references

CONIFERYL ALCOHOL (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3/b3-2+

1 reference

CONIFERYL ALCOHOL (English)

19 November 2016

2 references

SCHEMBL177684

2 references

MSBNK-Osaka_Univ-OUF00142

1 reference

MassBank accession ID

0 references

SPLASH

splash10-0udi-1971000000-886be2fff2ae0775e29a

0 references

splash10-0udl-2892000000-8e09702bbe43408dea53

0 references

splash10-0f80-9700000000-1f147bafa37d424b58e0

0 references

DSSTox substance ID

DTXSID50186489

2 references

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

DSSTOX compound identifier

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.260.977

29 December 2019

ECHA Substance Infocard ID

4-[(1E)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenol (English)

quotation

CAS no.: 32811-40-8 (English)

100.260.977

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.260.977

29 December 2019

4-[(1E)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenol (English)

quotation

CAS no.: 32811-40-8 (English)

RxNorm ID

1309334

1 reference

Global Substance Registration System

UNII

E7SM92591P

coniferyl alcohol (English)

Human Metabolome Database ID

19 November 2016

HMDB0012915

2 references

3 references

coniferol (English)

19 October 2016

C00043990

2 references

UNII

E7SM92591P

2 references

Global Substance Registration System

UNII

E7SM92591P

coniferyl alcohol (English)

19 November 2016

Natural Product Atlas ID

NPA019705

2 references

Immune Epitope Database and Analysis Resource

0 references

0 references

1 reference

1 March 2022

0 references

Brockhaus Enzyklopädie online ID

0 references

0 references

1 reference

28 October 2013

Microsoft Academic ID

0 references

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

3TKY (English)

19 October 2016

1 reference

5CVV (English)

19 October 2016

1 reference

4EVI (English)

19 October 2016

1 reference

5CVJ (English)

19 October 2016

1 reference