vanillin (Q33495)

participant

1 reference

Gene Ontology release 2019-11-16

vanillin biosynthetic process

product

1 reference

vanillin catabolic process

reactant

1 reference

vanillyl-alcohol oxidase activity

1 reference

lignostilbene alpha beta-dioxygenase activity

1 reference

vanillin synthase activity

1 reference

vanillin dehydrogenase activity

1 reference

reactive-black-5:hydrogen-peroxide oxidoreductase activity

1 reference

reference URL

http://geneontology.org/external2go/rhea2go

1 February 2021

chemical structure

Vanillin2.svg
828 × 881; 575 bytes

1 reference

image

Vanillin by Danny S. - 001.JPG
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0 references

mass

152.047 dalton

1 reference

vanillin (English)

19 October 2016

C₈H₈O₃

1 reference

vanillin (English)

19 November 2016

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

1 reference

vanillin (English)

19 November 2016

1.056 gram per cubic centimetre

1 reference

melting point

80 degree Celsius

1 reference

82 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

boiling point

285 degree Celsius

1 reference

flash point

147 degree Celsius

1 reference

safety classification and labelling

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response

1

1

0

no value

1 reference

Chemical composition of the volatiles ofDecalepis hamiltonii (Wight & Arn)

1 reference

Gossypium hirsutum

2 references

Lignin of the cotton plant of variety Tashkent 6

Survey of the volatile constituents of cotton lint and waste with regard to byssinosis

Vanilla planifolia

14 references

Determination of coumarin as an adulterant in vanilla flavoring products by high-performance liquid chromatography

Phenylpropanoid metabolism inVanilla planifolia Andr. (V) high performance liquid chromatographic analysis of phenolic glycosides and aglycones in developing fruits

Effect of light on vanillin precursors formation by in vitro cultures of Vanilla planifolia

Coumarin in vanilla extracts: Its detection and significance

Micellar electrokinetic chromatography as a screening method for the analysis of vanilla flavourings and vanilla extracts

Analysis of vanilla essences by high-performance liquid chromatography

Use of organized viable vanilla plant aerial roots for the production of natural vanillin

Determination of Glucovanillin and Vanillin in Cured Vanilla Pods

Some benzyl ethers present in the extract of vanilla (Vanilla planifolia)

Progress in the Authenticity Assessment of Vanilla. 1. Initiation of Authenticity Profiles

Localization of beta-D-glucosidase activity and glucovanillin in vanilla bean (Vanilla planifolia Andrews).

Bioactive aromatic compounds from leaves and stems of Vanilla fragrans

Vanillin biosynthetic pathways in plants

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

Cinnamomum zeylanicum

1 reference

Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils

Euploea sylvester

1 reference

Volatile compounds from androconial organs of danaine and ithomiine butterflies

Thapsia garganica

1 reference

Essential Oil of Thapsia garganica

common sunflower

1 reference

Isolation and identification of volatile constituents of sunflowers (Helianthus annuus L.)

Prunus armeniaca

1 reference

Glycosidically bound aroma compounds in the fruits of Prunus species: apricot (P. armeniaca, L.), peach (P. persica, L.), yellow plum (P. domestica, L. ssp. syriaca)

Prunus persica

1 reference

Glycosidically bound aroma compounds in the fruits of Prunus species: apricot (P. armeniaca, L.), peach (P. persica, L.), yellow plum (P. domestica, L. ssp. syriaca)

Prunus domestica

1 reference

Glycosidically bound aroma compounds in the fruits of Prunus species: apricot (P. armeniaca, L.), peach (P. persica, L.), yellow plum (P. domestica, L. ssp. syriaca)

Vanilla tahitensis

1 reference

Progress in the Authenticity Assessment of Vanilla. 1. Initiation of Authenticity Profiles

Festuca arundinacea

1 reference

Composition of essential oil of tall fescue

Aristolochia asclepiadifolia

1 reference

The composition of the essential oil fromAristolochia asclepiadifolia Brandg. root

Scutellaria baicalensis

1 reference

Essential oil of Scutellaria baicalensis G.

Populus deltoides

1 reference

Phenolic Composition of Bud Exudates of Populus deltoides

Populus euphratica

2 references

Analysis of phenolics of bud exudate of Populus euphratica by GC-MS

Components of the heartwood of Populus euphratica from an ancient tomb

Basella alba

1 reference

Volatile flavor components of malabar-nightshade (Basella rubra L.)

Lonicera microphylla

1 reference

Polyphenols ofLonicera microphylla

Quercus suber

2 references

Low Molecular Weight Polyphenols in Cork ofQuercus suber

Polyphenolic Composition ofQuercus suberCork from Different Spanish Provenances

Posidonia oceanica

1 reference

Distribution of phenolic compounds in the seagrass Posidonia oceanica

Curcuma longa

2 references

Characterization of powdered turmeric by liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry

High Performance Liquid Chromatographic Analysis of Curcuminoids and Their Photo-oxidative Decomposition Compounds in Curcuma Longa L

Nicotiana tabacum

2 references

Trace Analysis of Vanillin in Tobacco

Comparison of different extraction methods: steam distillation, simultaneous distillation and extraction and headspace co-distillation, used for the analysis of the volatile components in aged flue-cured tobacco leaves

Quercus robur

1 reference

Low Molecular Weight Phenolic Compounds in Spanish Oak Woods

Quercus pyrenaica

1 reference

Low Molecular Weight Phenolic Compounds in Spanish Oak Woods

Quercus faginea

1 reference

Low Molecular Weight Phenolic Compounds in Spanish Oak Woods

Zizania aquatica

1 reference

Wild Rice Hull Antioxidants†

Vanilla pompona

1 reference

Compounds of Vanillons(Vanilla pomponaSchiede)

Spartina cynosuroides

1 reference

Investigation of the Constituents and Antitumor Activity of Spartina cynosuroides

Abies sachalinensis

2 references

Plant constituents biologically active to insects. II. Juvabione analogs from Abies sachalinensis Mast. (1).

Occurrence of epijuvabione-type sesquiterpenoids in Abies sachalinensis

Piptocarpha opaca

1 reference

Piptocarphol esters from Piptocarpha opaca

Angelica sinensis

2 references

Serotonergic activity-guided phytochemical investigation of the roots of Angelica sinensis

GABAergic phthalide dimers from Angelica sinensis (Oliv.) Diels

Annona purpurea

4 references

New alkaloids from Annona purpurea

Four alkaloids from Annona cherimola.

Tryptamine-derived amides and alkaloids from the seeds of Annona atemoya.

Antiplatelet aggregation constituents from Annona purpurea

Arabidopsis thaliana

1 reference

Universally occurring phenylpropanoid and species-specific indolic metabolites in infected and uninfected Arabidopsis thaliana roots and leaves.

Aristolochia heterophylla

2 references

The constituents of the root and stem of Aristolochia heterophylla Hemsl

2,3-Dihydrobenzofuran neolignans from Aristolochia pubescens

Aristolochia pubescens

2 references

2,3-Dihydrobenzofuran neolignans from Aristolochia pubescens

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Begonia nantoensis

2 references

Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis

Cytotoxic and anti-HIV Principles from the Rhizomes of Begonia nantoensis.

Cassytha filiformis

1 reference

Chemical constituents from Cassytha filiformis II

Chaerophyllum hirsutum

1 reference

Cytotoxic constituents of roots of Chaerophyllum hirsutum

Cinnamomum subavenium

2 references

Cytotoxic constituents from the leaves of Cinnamomum subavenium

Cytotoxic constituents of the stems of Cinnamomum subavenium

Curcuma comosa

1 reference

Structures of new monoterpenes from Thai herbal medicine Curcuma comosa

Ferula assa-foetida

1 reference

Influenza A (H(1)N(1)) Antiviral and Cytotoxic Agents from Ferula assa-foetida.

Gynura elliptica

1 reference

Anti-platelet aggregation constituents from Gynura elliptica

Hibiscus taiwanensis

2 references

Constituents from the stems of Hibiscus taiwanensis.

Constituents from the Stems of Hibiscus taiwanensis.

Ligularia dentata

2 references

Constituents of the roots of Ligularia dentata Hara

Constituents of the leaves and roots of Ligularia stenocephala MATSUM. et KOIDZ.

Ligularia stenocephala

2 references

Constituents of the leaves and roots of Ligularia stenocephala MATSUM. et KOIDZ.

Constituents of the roots of Ligularia dentata Hara

Microtropis japonica

2 references

Dihydroagarofuranoid sesquiterpenes, a lignan derivative, a benzenoid, and antitubercular constituents from the stem of Microtropis japonica

New dihydroagarofuranoid sesquiterpenes, a lignan derivative, benzenoid, and antitubercular constituents from the stem of Microtropis japonica

Morinda citrifolia

5 references

Lipoxygenase inhibitory constituents of the fruits of noni (Morinda citrifolia) collected in Tahiti.

An anthraquinone with potent quinone reductase-inducing activity and other constituents of the fruits of Morinda citrifolia (noni).

Lipoxygenase Inhibitory Constituents of the Fruits of Noni (Morinda citrifolia) Collected in Tahiti

Anthraquinones with quinone reductase-inducing activity and benzophenones from Morinda citrifolia (noni) roots.

Chemical Constituents from the Stems of Morinda citrifolia Linn

Phoebe formosana

1 reference

Laurodionine, a New Oxalyl-fused Aporphine Alkaloid fromPhoebe formosana

Phyllanthus oligospermus

1 reference

Cytotoxic arylnaphthalene lignans from Phyllanthus oligospermus

Pimenta dioica

1 reference

Antioxidative phenylpropanoids from berries of Pimenta dioica

Pseudotsuga sinensis var. sinensis

1 reference

Terpenoids and flavonoids from Pseudotsuga wilsoniana

Rhus chinensis

1 reference

Rhusemialins A-C, new cyclolignan esters from the roots of Rhus javanica var. roxburghiana

Taraxacum formosanum

1 reference

Chemical constituents from roots of Taraxacum formosanum

Tetracentron sinense

1 reference

Two glycosides from the stem bark of Tetracentron sinense.

Tribulus terrestris

1 reference

Alkaloids and other constituents from Tribulus terrestris

Viscum articulatum

2 references

The inhibition of superoxide anion generation by neutrophils from Viscum articulactum

The inhibition of superoxide anion generation in human neutrophils by Viscum coloratum

Viscum coloratum

2 references

The inhibition of superoxide anion generation in human neutrophils by Viscum coloratum

The inhibition of superoxide anion generation by neutrophils from Viscum articulactum

Haplopteris anguste-elongata

1 reference

Constituents of Vittaria anguste-elongata and their biological activities

Zanthoxylum wutaiense

2 references

Constituents of the root wood of Zanthoxylum wutaiense with antitubercular activity

Neolignans, a coumarinolignan, lignan derivatives, and a chromene: anti-inflammatory constituents from Zanthoxylum avicennae

maize

2 references

Chemical constituents of the style of Zea mays L. with glycation inhibitory activity

Volatile Flavor Components of Corn Tortillas and Related Products

Abies nephrolepis

2 references

Lignans from Abies nephrolepis and Picea ajanensis

Phenolic compounds of Abies nephrolepis and their NO production inhibitory activities.

Ailanthus integrifolia

1 reference

Studies on the constituents of Ailanthus integrifolia

Allagopappus dichotomus

1 reference

Sesquiterpene Lactones and Other Constituents of Allagopappus Species

Annona cherimola

2 references

Cheritamine, A NewN-Fatty Acyl Tryptamine and Other Constituents from the Stems ofAnnona cherimola

Annocherine C, A New C-α Hydroxy Benzylisoquinoline and Other Constituents from the Leaves ofAnnona Cherimola

Aralia bipinnata

2 references

Lignans from the wood of Aralia bipinnata

Phenylpropanoids from Aralia bipinnata

Araucaria angustifolia

1 reference

Phenylpropanoid derivatives and biflavones at different stages of differentiation and development of Araucaria angustifolia

Artemisia annua

1 reference

Coniferaldehyde derivatives from tissue culture of Artemisia annua and Tanacetum parthenium

Artemisia capillaris

1 reference

New constituents and antiplatelet aggregation and anti-HIV principles of Artemisia capillaris

Artemisia japonica

1 reference

Phytochemical constituents of Artemisia japonica ssp. littoricola

Artemisia scoparia

1 reference

Extractives of Artemisia scoparia

Artemisia stolonifera

1 reference

Phytochemical constituents of Artemisia stolonifera

Brucea javanica

3 references

Bioactive constituents of the seeds of Brucea javanica

Separation and Determination of Chemical Constituents in the Roots ofRhus JavanicaL. Var.Roxburghiana

Rhusemialins A-C, new cyclolignan esters from the roots of Rhus javanica var. roxburghiana

Capsicum annuum var. annuum

1 reference

Biotransformation of ferulic acid and vanillylamine to capsaicin and vanillin in immobilized cell cultures of Capsicum frutescens

Centaurea calcitrapa

1 reference

Chemical constituents of Centaurea cadmea

Centaurea ornata

1 reference

Guaianolides and eudesmanolides from Centaurea ornata

Centaurea scoparia

2 references

Chemical constituents of Centaurea cadmea

Constituents of the Egyptian Centaurea scoparia. III. Phenolic constituents of the aerial parts

Chamaecrista flexuosa

1 reference

Unusual cassanes from a Chamaecrista species

Chuquiraga atacamensis

1 reference

CONSTITUENTS OF CHUQUIRAGA ATACAMENSIS AND C. ULICINA

Cinnamomum kotoense

2 references

Antitubercular constituents from the stem wood of Cinnamomum kotoense

Chemical and cytotoxic constituents from the leaves of Cinnamomum kotoense

Colchicum bornmuelleri

1 reference

Alkaloids and phenolics of Colchicum turcicum

Colchicum kotschyi

1 reference

Alkaloids and phenolics of Colchicum turcicum

Lepidothamnus intermedius

1 reference

Chemistry of the Podocarpaceae. LXIX. Further Lignans from te Wood of Dacrydium intermedium

Uvariopsis tripetala

2 references

Chromone and Phenanthrene Alkaloids from Dennettia tripetala.

Chromone and phenanthrene alkaloids from Dennettia tripetala

Eleutherococcus senticosus

1 reference

Phenolic compounds of Eleutherococcus senticosus

Euchresta formosana

3 references

Heartwood constituents ofPinus formosana

Antiplatelet and Anti-HIV Constituents from Euchresta Formosana

The Constituents of Euchresta Formosana

Euphorbia quinquecostata

1 reference

New chemical constituents of Euphorbia quinquecostata and absolute configuration assignment by a convenient Mosher ester procedure carried out in NMR tubes.

Gastrodia elata

6 references

Anti-inflammatory action of phenolic compounds from Gastrodia elata root

Inhibitory effects of constituents of Gastrodia elata Bl. on glutamate-induced apoptosis in IMR-32 human neuroblastoma cells

Identification and determination of active components in Gastrodia elata Bl. by capillary electrophoresis

Determination of the active ingredients in Gastrodia rhizoma by capillary electrophoresis with electrochemical detection

In vitro Effects of Hydroxybenzaldehydes from Gastrodia elata and their Analogues on GABAergic Neurotransmission, and a Structure-Activity Correlation

Two New Phenolic Compounds from the Rhizomes of Gastrodia elataBlume

Geijera balansae

1 reference

Plantes de Nouvelle-Calédonie, XCVI. Alcaloïdes de Geijera balansae

Helianthus heterophyllus

1 reference

Heliangolides, kauranes and other constituents of Helianthus heterophyllus

Helianthus petiolaris

2 references

New sesquiterpene lactones and other constituents from Fitchia speciosa

New Sesquiterpene Lactones and Other Constituents from Helianthus petiolaris

Hibiscus cannabinus

1 reference

Phenolic constituents from the core of kenaf (Hibiscus cannabinus).

Houttuynia cordata

2 references

The constituents and their bioactivities of Houttuynia cordata

Anti-complementary constituents of Houttuynia cordata and their targets in complement activation cascade

Lagotis yunnanensis

2 references

Constituents of Lagotis yunnanensis

Study on Chemical Constituents of Lagotis yunnanensis

Conioselinum anthriscoides

2 references

Simultaneous analysis of seventeen chemical ingredients of Ligusticum chuanxiong by on-line high performance liquid chromatography-diode array detector-mass spectrometry

Studies on chemical constituents of Illicium simonsii

Ligusticum chuanxiong

2 references

Simultaneous analysis of seventeen chemical ingredients of Ligusticum chuanxiong by on-line high performance liquid chromatography-diode array detector-mass spectrometry

Studies on chemical constituents of Illicium simonsii

Magnolia crassipes

1 reference

Phenolic constituents from Oplopanax horridus

Melia azedarach

4 references

Effects of Melia azedarach on Triatoma infestans

Antifungal Effects of Different Organic Extracts from Melia azedarach L. on Phytopathogenic Fungi and Their Isolated Active Components

Antifungal synergistic effect of scopoletin, a hydroxycoumarin isolated from Melia azedarach L. fruits

Über einige Inhaltsstoffe der Früchte und Wurzel von Melia azedarach L.

Colchicum manissadjianii

1 reference

Alkaloids and phenolics of three Merendera species

Mikania microptera

1 reference

Sesquiterpene lactones and other constituents of Mikania rimachii and Mikania microptera

Mikania rimachii

1 reference

Sesquiterpene lactones and other constituents of Mikania rimachii and Mikania microptera

Nectandra oppositifolia

1 reference

Antitumor plants. X. Constituents of Nectandra rigida

Ocimum tenuiflorum

2 references

Leishmanicidal active constituents from Nepalese medicinal plant Tulsi (Ocimum sanctum L.).

New Constituents from Ocimum sanctum

Onobrychis meschetica

1 reference

Substances detected on the surface of the roots of various species of the genus Onobrychis adans and in the soil surrounding them

Paeonia clusii

1 reference

Paeonicluside, a new salicylic glycoside from the Greek endemic species Paeonia clusii.

Pandanus odoratissimus

1 reference

Antioxidative Activities of constituents Isolated from Pandanus odoratissimus

Pedalium murex

1 reference

Heptatriacontan-4-one, tetratriacontanyl octacosanoate and other constituents from Pedalium murex

Petasites formosanus

1 reference

The bakkenolides from the root of Petasites formosanus and their cytotoxicity

Korean Spruce

1 reference

Lignans from the wood of Picea koraiensis

Picea obovata

1 reference

Lignans from the wood of Picea koraiensis

Populus grandidentata

1 reference

A Novel Caffeic Acid Derivative and Other Constituents of Populus Bud Excretion and Propolis (Bee-Glue)

Psilostrophe cooperi

1 reference

Modified helenanolides from Psilostrophe gnaphaloides and Psilostrophe cooperi

Robinsonia thurifera

1 reference

Kaurane derivatives from Robinsonia evenia

Rolandra fruticosa

1 reference

Sesquiterpene lactones from Rolandra fruticosa

Scutellaria chaematochlora

1 reference

A New Neoclerodane Diterpenoid from Scutellaria hematochlora

Scutellaria haematochlora

1 reference

A New Neoclerodane Diterpenoid from Scutellaria hematochlora

Solanum melongena

3 references

Fungitoxic compounds from the roots of the eggplant stock.

Three New Phenolic Amides from the Roots of Eggplant (Solanum melongenaL.)

Three new phenolic amides from the roots of eggplant (Solanum melongena L.).

Tabernaemontana glandulosa

1 reference

Indole alkaloids fromTabernaemontana glandulosa

Tetradium glabrifolium

1 reference

The heartwood constituents of Tetradium glabrifolium

Tinospora crispa

1 reference

Antioxidant and lipophilic constituents of Tinospora crispa

Xanthium spinosum

1 reference

Xanthanolides from Xanthium spinosum

Zingiber zerumbet

1 reference

Flavonoids and aromatic compounds from the rhizomes of Zingiber zerumbet

Anastatica hierochuntica

2 references

Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells

Anastatins A and B, new skeletal flavonoids with hepatoprotective activities from the desert plant Anastatica hierochuntica.

Beilschmiedia tsangii

2 references

Anti-inflammatory Endiandric Acid Analogues from the Roots of Beilschmiedia tsangii

New cytotoxic tetrahydrofuran- and dihydrofuran-type lignans from the stem of Beilschmiedia tsangii

Panax bipinnatifidus var. bipinnatifidus

1 reference

Bioactive Constituents from the Roots of Panax japonicus var. major and Development of a LC-MS/MS Method for Distinguishing between Natural and Artifactual Compounds

Pisonia aculeata

1 reference

Antitubercular Chromones and Flavonoids from Pisonia aculeata

Stellaria dichotoma

2 references

Structures of new beta-carboline-type alkaloids with antiallergic effects from Stellaria dichotoma(1,2)

Bioactive constituents from Chinese natural medicines. XIV. New glycosides of beta-carboline-type alkaloid, neolignan, and phenylpropanoid from Stellaria dichotoma L. var. lanceolata and their antiallergic activities.

Avena sativa

2 references

Antioxidant capacity of oat (Avena sativa L.) extracts. 2. In vitro antioxidant activity and contents of phenolic and tocol antioxidants

Variation in Oat Groats Due to Variety, Storage and Heat Treatment. I: Phenolic Compounds

Brassica napus

1 reference

Determination of antioxidant compounds and antioxidant activity in commercial oilseeds for food use

Olea europaea

11 references

Analysis by liquid chromatography-tandem mass spectrometry of biophenolic compounds in olives and vegetation waters, Part I

Analysis by liquid chromatography-tandem mass spectrometry of biophenolic compounds in virgin olive oil, Part II

Changes in commercial virgin olive oil (cv Arbequina) during storage, with special emphasis on the phenolic fraction

Determination of antioxidant compounds and antioxidant activity in commercial oilseeds for food use

Effect of irrigation applied to olive trees (Olea europaea L.) on phenolic compound transfer during olive oil extraction

Effect of the Maturation Process of the Olive Fruit on the Phenolic Fraction of Drupes and Oils from Arbequina, Farga, and Morrut Cultivars

Phenolic compounds profile of cornicabra virgin olive oil.

PHENOLIC COMPOUNDS, TOCOPHEROLS AND OTHER MINOR COMPONENTS IN VIRGIN OLIVE OILS OF SOME TUNISIAN VARIETIES

Retention and distribution of natural antioxidants (α-tocopherol, polyphenols and terpenic acids) after shallow frying of vegetables in virgin olive oil

Transfer of phenolic compounds during olive oil extraction in relation to ripening stage of the fruit

Use Lactobacillus plantarum in olive oil process and improvement of phenolic compounds content

Secale cereale

1 reference

Hydroxycinnamic acid composition and in vitro antioxidant activity of selected grain fractions

cacao

1 reference

Thin-layer high-vacuum distillation to isolate volatile flavour compounds of cocoa powder

Streptomyces griseus

2 references

Characterization of two Streptomyces enzymes that convert ferulic acid to vanillin

Production and genetic improvement of a novel antimycotic agent, saadamycin, against dermatophytes and other clinical fungi from endophytic Streptomyces sp. Hedaya48.

Streptomyces setonii

2 references

Characterization of two Streptomyces enzymes that convert ferulic acid to vanillin

Production and genetic improvement of a novel antimycotic agent, saadamycin, against dermatophytes and other clinical fungi from endophytic Streptomyces sp. Hedaya48.

Abies sibirica

1 reference

Vanillin and veratraldehyde fromAbies sibirica

Aegle marmelos

1 reference

Antifungal constituents isolated from the seeds of Aegle marmelos

Angelica pachycarpa

1 reference

Coumarins of Angelica pachycarpa Fruits

Antidesma montanum var. montanum

1 reference

Chemical Constituents from the Root ofAntidesma Pentandrumvar.Barbatum

Antidesma pentandrum var. barbatum

1 reference

Chemical Constituents from the Root ofAntidesma Pentandrumvar.Barbatum

Arcangelisia flava

1 reference

Furanoditerpenes from Arcangelisia flava (L.) Merr. and their antifungal activity

Sweet Woodruff

1 reference

Naturally occurring quinones. Part XIII. Anthraquinones and related naphthalenic compounds in Galium spp. and in Asperula odorata

Aster indicus

1 reference

Phenolic derivatives from Aster indicus

Beta vulgaris

1 reference

Phenolic germination inhibitors in the seed balls of red beet (Beta vulgaris L. var. rubra).

Carissa edulis

1 reference

Lignans and other constituents from Carissa edulis

Carissa spinarum

1 reference

Lignans and other constituents from Carissa edulis

Carya cathayensis

1 reference

New antitumor compounds from Carya cathayensis

Chlorophytum inornatum

1 reference

Phytochemistry and antimycobacterial activity of Chlorophytum inornatum

Echinacea purpurea

1 reference

Further amides from Echinacea purpurea

Engelhardia roxburghiana

1 reference

Secondary metabolites from the roots of Engelhardia roxburghiana and their antitubercular activities

Fibraurea tinctoria

1 reference

Anti-inflammatory activities of furanoditerpenoids and other constituents from Fibraurea tinctoria

Ficus erecta var. beecheyana

1 reference

New Prenylated Flavones from the Roots ofFicus Beecheyana

Ficus nervosa

1 reference

Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa

Strobilanthes psilostachys

1 reference

Novel cadinane and norcadinane sesquiterpenes and a new propanoate from Goldfussia psilostachys

Hyoscyamus niger

2 references

Hyosgerin, a new optically active coumarinolignan, from the seeds of Hyoscyamus niger

Hyosmin, a New Lignan from Hyoscyamus Niger L

Ilex pubescens

1 reference

Two New 2-Phenylethyl Alcohol Derivatives and One New Lignan Derivative from the Root ofIlex pubescens

Duhaldea cappa

1 reference

Chemical constituents from Inula cappa

Juniperus communis

1 reference

New phenylpropanoid glycosides from Juniperus communis var. depressa

Juniperus communis depressa

1 reference

New phenylpropanoid glycosides from Juniperus communis var. depressa

Lagochilus leiacanthus

1 reference

Studies on the Constituents of Lagochilus leiacanthus (Labiatae)

Licaria triandra

1 reference

Cytotoxic constituents of the stem bark of Neolitsea acuminatissima

Machilus zuihoensis

1 reference

Chemical constituents from the leaves of Machilus zuihoensis Hayata var. mushaensis (Lu) Y.C. Liu.

Melicope semecarpifolia

1 reference

Cytotoxic and anti-platelet aggregation constituents from the root wood of Melicope semecarpifolia

Mondia whitei

1 reference

A chlorinated coumarinolignan from the African medicinal plant, Mondia whitei

Myriactis humilis

1 reference

Cytotoxic chromenes from Myriactis humilis

Neolitsea acuminatissima

1 reference

Cytotoxic constituents of the stem bark of Neolitsea acuminatissima

Neolitsea hiiranensis

1 reference

Secondary metabolites from the leaves of Neolitsea hiiranensis and the anti-inflammatory activity of some of them

Panax japonicus

2 references

Bioactive Constituents from the Roots of Panax japonicus var. major and Development of a LC-MS/MS Method for Distinguishing between Natural and Artifactual Compounds

Potent alpha-glucosidase inhibitors from the roots of Panax japonicus C. A. Meyer var. major

Picea glauca

1 reference

Comparison of phenolic compounds from galls and shoots of Picea glauca

1 reference

1 reference

Chemical constituents from Saussurea cordifolia

Securidaca inappendiculata

1 reference

Three New Compounds fromSecuridaca inappendiculata

Tolpis webbii

1 reference

Chemical constituents of Tolpis species

Vernonanthura chamaedrys

2 references

Glaucolides and related sesquiterpene lactones from Vernonia chamaedrys

Diterpenes from Vernonanthura amplexicaulis

Xanthium strumarium

1 reference

(-)-Xanthienopyran, a new inhibitor of superoxide anion generation by activated neutrophils, and further constituents of the seeds of Xanthium strumarium.

Zanthoxylum ailanthoides

2 references

Two new sesquiterpenoids and anti-HIV principles from the root bark of Zanthoxylum ailanthoides

Chemical Constituents from the Root Bark of FormosanZanthoxylum Ailanthoides

Zanthoxylum beecheyanum

1 reference

Chemical and Antiplatelet Constituents from the Stem ofZanthoxylum Beecheyanum

Zanthoxylum integrifoliolum

1 reference

Chemical Constituents from the Root Wood ofZanthoxylum Integrifoliolum

Hijmania turbinata

1 reference

Inhibition of MMP-2 secretion from brain tumor cells suggests chemopreventive properties of a furanocoumarin glycoside and of chalcones isolated from the twigs of Dorstenia turbinata

Euphorbia hirsuta

1 reference

Bioactive diterpenoids, a new jatrophane and two ent-abietanes, and other constituents from Euphorbia pubescens

Pinus sylvestris

1 reference

Phenolic extractives from the bark of Pinus sylvestris L. and their effects on inflammatory mediators nitric oxide and prostaglandin E2.

Chamaecyparis formosensis

1 reference

Effects of Chamaecyparis formosensis Matasumura extractives on lipopolysaccharide-induced release of nitric oxide

Spiraea

1 reference

New neolignans from Spiraea formosana

Gynura segetum

1 reference

Anti-platelet aggregation constituents from Gynura elliptica

Aeschynanthus bracteatus

1 reference

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

Leptotes bicolor

1 reference

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

Pinus tabuliformis

1 reference

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

Orobanche crenata

1 reference

Phenolic metabolites from Orobanche speciosa

Strobilanthes dimorphotricha

1 reference

Novel cadinane and norcadinane sesquiterpenes and a new propanoate from Goldfussia psilostachys

Artemisia argyi

1 reference

Phytochemical constituents of Artemisia stolonifera

Isatis quadrialata

2 references

Comparison of Antioxidative Activity of Phenolic Compounds in Boreava orientalis and Their Related Compound.

Antioxidative Activity of Phenolic Compounds of Boreava orientalis.

Aristolochia elegans

1 reference

The alkaloids and other constituents from the root and stem of Aristolochia elegans

Juniperus communis var. depressa

1 reference

New phenylpropanoid glycosides from Juniperus communis var. depressa

Marsypopetalum modestum

1 reference

Chemical constituents of the stem of Marsypopetalum modestum and their bioactivities

Schizosaccharomyces pombe

1 reference

De novo biosynthesis of vanillin in fission yeast (Schizosaccharomyces pombe) and baker's yeast (Saccharomyces cerevisiae)

Curculigo capitulata

2 references

Antioxidative phenols and phenolic glycosides from Curculigo orchioides

Norneolignan and phenols from Curculigo capitulata

Picris spinifera

1 reference

A eudesmanolide from Picris spinifera

Beilschmiedia erythrophloia

1 reference

Endiandric Acid Analogues from the Roots of Beilschmiedia erythrophloia

Orobanche variegata

1 reference

Phenolic metabolites from Orobanche speciosa

Hydnora johannis

1 reference

Antibacterial activity, cytotoxicity and chemical constituents of Hydnora johannis roots

Hydnora abyssinica

1 reference

Antibacterial activity, cytotoxicity and chemical constituents of Hydnora johannis roots

garlic

1 reference

Composition of Polyphenols and Antioxidant Activity of Garlic Bulbs Collected from Different Locations of Korea

Mangifera indica

1 reference

Food quality and nutraceutical value of nine cultivars of mango (Mangifera indica L.) fruits grown in Mediterranean subtropical environment

Apium graveolens

2 references

The impact of steam-blanching and dehydration on phenolic, organic acid composition, and total carotenoids in celery roots

Potent odorants characterize the aroma quality of leaves and stalks in raw and boiled celery

asparagus

1 reference

Characterization of Cell Wall Components and Their Modifications during Postharvest Storage of Asparagus officinalis L.: Storage-Related Changes in Dietary Fiber Composition

Humulus lupulus

1 reference

Characterization of Key Aroma Compounds in Pellets of Different Hop Varieties (Humulus lupulus L.) by Means of the Sensomics Approach

Momordica charantia

1 reference

Establishment of Momordica charantia hairy root cultures for the production of phenolic compounds and determination of their biological activities

Medicago sativa

1 reference

Soluble phenolic monomers in forage crops

Phaseolus vulgaris

1 reference

Total Phenolic, Phenolic Acid, Anthocyanin, Flavan-3-ol, and Flavonol Profiles and Antioxidant Properties of Pinto and Black Beans ( Phaseolus vulgaris L.) as Affected by Thermal Processing

basil

1 reference

Chemical composition and antioxidant capacity of free volatile aglycones from basil (Ocimum basilicum L.) compared with its essential oil

Picea abies

2 references

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

Changes in humic substances along an age sequence of Norway spruce stands planted on former agricultural land

Triticum aestivum

1 reference

Identification and quantitation of lipophilic extractives from wheat straw

Zingiber officinale

2 references

Metabolic Profiles of Ginger, A Functional Food, and Its Representative Pungent Compounds in Rats by Ultraperformance Liquid Chromatography Coupled with Quadrupole Time-of-Flight Tandem Mass Spectrometry.

Anti-Platelet Aggregation and Vasorelaxing Effects of the Constituents of the Rhizomes of Zingiber officinale

Couroupita guianensis

1 reference

Volatile Constituents of Couroupita guianensis Aubl. Flowers

Eryngium foetidum

1 reference

Composition of the Leaf and Root Oils of Eryngium foetidum L.

Zingiber purpureum

1 reference

Further characterization of the constituents of a thai medicinal plant, Zingiber cassumunar Roxb.

Zingiber montanum

1 reference

Further characterization of the constituents of a thai medicinal plant, Zingiber cassumunar Roxb.

Zingiber cassumunar

1 reference

Further characterization of the constituents of a thai medicinal plant, Zingiber cassumunar Roxb.

Eurycoma longifolia

1 reference

NF-κB inhibitors from Eurycoma longifolia

Cryptocarya chinensis

1 reference

Cytotoxic flavonoids from the leaves of Cryptocarya chinensis

Taraxacum mongolicum

1 reference

Chemical constituents from roots of Taraxacum formosanum

Cinnamon

1 reference

Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils

Colchicum speciosum

1 reference

Alkaloids and phenolics of Colchicum turcicum

Gynura japonica

2 references

Anti-platelet aggregation constituents from Gynura elliptica

Anti-platelet aggregation and chemical constituents from the rhizome of Gynura japonica.

Pandanus tectorius

1 reference

Antioxidative Activities of constituents Isolated from Pandanus odoratissimus

Aristolochia kaempferi

3 references

2,3-Dihydrobenzofuran neolignans from Aristolochia pubescens

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Constituents from the stem and root of Aristolochia kaempferi

Aristolochia littoralis

1 reference

The alkaloids and other constituents from the root and stem of Aristolochia elegans

Ligusticum striatum

2 references

Simultaneous analysis of seventeen chemical ingredients of Ligusticum chuanxiong by on-line high performance liquid chromatography-diode array detector-mass spectrometry

Studies on chemical constituents of Illicium simonsii

Malus pumila

1 reference

Headspace and essential oil analysis of apple flowers

tomato

2 references

Phenolics of suberized envelopes generated by isolated tomato locule protoplasts

Fungitoxic Compounds from the Roots of Tomato Stock.

Quercus petraea

1 reference

Low Molecular Weight Phenolic Compounds in Spanish Oak Woods

Oreocome striata

1 reference

DETERMINATION OF THE ACTIVE INGREDIENTS IN CHUANXIONG BY HPLC, HPLC-MS, AND EI-MS

Handroanthus impetiginosum

1 reference

Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique

Handroanthus impetiginosus

1 reference

Structure Determination of New Isomeric Naphtho[2,3-b]furan-4,9-diones fromTabebuia avellanedae by the selective-INEPT technique

Pandanus odorifer

1 reference

Antioxidative Activities of constituents Isolated from Pandanus odoratissimus

Vertebrata lanosa

1 reference

In-vitro cytotoxic activities of the major bromophenols of the red alga Polysiphonia lanosa and some novel synthetic isomers

Taxus wallichiana

2 references

Antiallergic activity of aqueous extracts and constituents of Taxus yunnanensis

Diterpenes and sesquiterpenes from the bark of Taxus yunnanensis

Apiaceae

2 references

Components of Cnidium officinale Makino: occurrence of pregnenolone, coniferyl ferulate, and hydroxyphthalides

Studies on the constituents of umbelliferae plants. XV Constituents of Cnidium officinale : Occurrence of pregnenolone, coniferylferulate and hydroxyphthalides.

Festuca rubra

1 reference

Composition of essential oil of tall fescue

Malus domestica

1 reference

Headspace and essential oil analysis of apple flowers

Strobilanthes pentstemonoides

1 reference

Novel cadinane and norcadinane sesquiterpenes and a new propanoate from Goldfussia psilostachys

Vitis vinifera

1 reference

RP-HPLC analysis of phenolic compounds and flavonoids in beverages and plant extracts using a CoulArray detector.

broad bean

4 references

The identification of gibberellins in immature seeds of Vicia faba, and some chemotaxonomic considerations

UHPLC-ESI-QTOF-MS-based metabolic profiling of Vicia faba L. (Fabaceae) seeds as a key strategy for characterization in foodomics

Fast responses of metabolites in Vicia faba L. to moderate NaCl stress

Kaempferol 3-O-Galactoside, 7-O-Rhamnoside is the Major Green Fluorescing Compound in the Epidermis of Vicia faba

Dendrobium hainanense

1 reference

Chemical constituents from Dendrobium hainanense

Dendrobium nobile

1 reference

A systematical review on ethnobotanical, phytochemical and pharmacological aspects of Dendrobium nobile Lindl.

physically interacts with

Transient receptor potential cation channel, subfamily V, member 3

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

6412

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

17 August 2016

1 reference

1 reference

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

1 reference

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

1 reference

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

1 reference

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

2 references

Identification of Amycolatopsis sp. strain HR167 genes, involved in the bioconversion of ferulic acid to vanillin

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

3 references

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

Functional analyses of genes involved in the metabolism of ferulic acid in Pseudomonas putida KT2440.

Biotransformation of isoeugenol to vanillin by Pseudomonas putida IE27 cells

2 references

Vanillin production using metabolically engineered Escherichia coli under non-growing conditions.

Biotransformation of isoeugenol to vanillin by Pseudomonas putida IE27 cells

3 references

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

Enhanced vanillin production from ferulic acid using adsorbent resin

Identification of Amycolatopsis sp. strain HR167 genes, involved in the bioconversion of ferulic acid to vanillin

1 reference

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

Production of vanillin from waste residue of rice bran oil by Aspergillus niger and Pycnoporus cinnabarinus

Pycnoporus cinnabarinus

fabrication method

bioengineering

1 reference

Vanillin-bioconversion and bioengineering of the most popular plant flavor and its de novo biosynthesis in the vanilla orchid

Production of vanillin from waste residue of rice bran oil by Aspergillus niger and Pycnoporus cinnabarinus

1 reference

Harnessing eugenol as a substrate for production of aromatic compounds with recombinant strains of Amycolatopsis sp. HR167

1 reference

Biotransformation of isoeugenol to vanillin by a novel strain of Bacillus fusiformis

1 reference

Biotransformation of isoeugenol to vanillin by a newly isolated Bacillus pumilus strain: Identification of major metabolites

1 reference

Metabolism of isoeugenol via isoeugenol-diol by a newly isolated strain of Bacillus subtilis HS8.

1 reference

Conversion of Isoeugenol to Vanillin by Psychrobacter sp. Strain CSW4

Pseudomonas chlororaphis

fabrication method

bioengineering

1 reference

Isolation and Identification of a Novel Strain of Pseudomonas chlororaphis Capable of Transforming Isoeugenol to Vanillin†

described by source

Armenian Soviet Encyclopedia, vol. 11

page(s)

277

0 references

anticonvulsant agent

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

15 March 2018

1 reference

2912.41.00

0 references

0 references

0 references

Vanillin

1 reference

Identifiers

GND ID

4572822-7

1 reference

Library of Congress authority ID

J9U ID

987007531845605171

0 references

sh85142054

0 references

InChI

InChI=1S/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H3

1 reference

vanillin (English)

19 November 2016

2 references

vanillin (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

121-33-5

2 references

vanillin (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=121-33-5

10 April 2021

1 reference

Vanillin (English)

19 November 2016

1 reference

vanillin (English)

19 November 2016

Reaxys registry number

472792

1 reference

vanillin (English)

19 October 2016

3596

0 references

ChEBI ID

18346

mapping relation type

2 references

VANILLIN (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H3

1 reference

VANILLIN (English)

19 November 2016

2 references

MSBNK-Fac_Eng_Univ_Tokyo-JP000532

1 reference

MassBank accession ID

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP009387

0 references

MSBNK-MetaboLights-ML005951

0 references

MSBNK-Washington_State_Univ-BML82325

0 references

MSBNK-Washington_State_Univ-BML82326

0 references

MSBNK-Washington_State_Univ-BML82327

0 references

MSBNK-Washington_State_Univ-BML82328

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP008443

0 references

SPLASH

splash10-0udi-7900000000-ee0a0ad1232fa889e567

0 references

splash10-0udi-9800000000-d8f749f48a78e7c9c3bf

0 references

splash10-0udr-0900000000-d67b08f1b4f6e90cd270

0 references

splash10-0udi-0900000000-622b9790eec89a48b1e7

0 references

splash10-0udi-0900000000-66ed3dbbb13436ca389e

0 references

splash10-0udi-0900000000-334e2cf1c60f75229fd1

0 references

splash10-0uy0-0900200200-4cbd13b45290ded181ee

0 references

splash10-0udi-0900000000-bf65345f0ffa2efeabbb

0 references

splash10-0006-9400000000-b896ee9971b06e2c9574

0 references

splash10-00kf-9000000000-6b6a9d0e55412cf051d6

0 references

splash10-00di-1960000000-b6678c7961ee7df779a1

0 references

splash10-00di-0900000000-3e7377f36ca2547f4885

0 references

splash10-000i-0900000000-28fea3ea6aa57be4b885

0 references

splash10-0udi-5900000000-907c9684d5ac0386d522

0 references

NMRShiftDB structure ID

10008648

1 reference

0 references

0 references

YW5775000

1 reference

ZVG number

492841

1 reference

Hazardous Substances Data Bank

1 reference

28 October 2019

VANILLIN (English)

10 May 2021

2 references

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

DSSTOX compound identifier

0 references

0 references

0 references

0 references

1 reference

vanillin (English)

ECHA Substance Infocard ID

19 November 2016

100.004.060

1 reference

reference URL

http://echa.europa.eu/de/information-on-chemicals/registered-substances

FL number

05.018

1 reference

quotation

CAS no.: 121-33-5 (English)

23 January 2021

05.018

1 reference

28 December 2019

VANILLIN (English)

CAS no.: 121-33-5 (English)

PesticideInfo chemical ID

0 references

1 reference

0 references

0 references

Guide to Pharmacology Ligand ID

6412

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

6412

vanillin (English)

19 November 2016

1 reference

14 March 2018

1 reference

vanillin (English)

Human Metabolome Database ID

19 November 2016

HMDB0012308

2 references

based on heuristic

3 references

vanillin (English)

19 October 2016

3 references

vanillin (English)

19 October 2016

2 references

vanillin (English)

19 November 2016

NDF-RT ID

N0000022791

1 reference

vanillin (English)

19 November 2016

0 references

1 reference

Encyclopædia Britannica Online ID

vanillin (English)

19 October 2016

0 references

29124100

0 references

science/vanillin

subject named as

vanillin

0 references

1 reference

28 October 2013

Great Russian Encyclopedia Online ID (old version)

1898816

subject named as

ВАНИЛИН

reason for deprecated rank

redirected to GRE portal

0 references

Great Russian Encyclopedia portal ID

0 references

0 references

889

1 reference

Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA)

13 May 2021

1 reference

9 July 2020

0 references

Microsoft Academic ID

2777340834

0 references

OmegaWiki Defined Meaning

0 references

1 reference

26 January 2022

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

1 reference

2VSU (English)

19 October 2016

1 reference

2VSS (English)

19 October 2016

1 reference

4RGS (English)

19 October 2016

1 reference

5FXP (English)

19 October 2016

Vanillin

0 references

1 reference

1 reference

Store norske leksikon (Great Norwegian Encyclopedia) ID

vanillin

mapping relation type

0 references

1 reference

inferred by common MeSH mappings on source and on Wikidata

vanillin (English)

19 November 2016

1 reference

UMLS 2023

25 May 2023

WordNet 3.1 Synset ID

12107549-n

1 reference