syringaldehyde (Q411695)

SYRINGALDEHYDE (English)

7 October 2016

chemical formula

C₉H₁₀O₄

1 reference

SYRINGALDEHYDE (English)

7 October 2016

canonical SMILES

COC1=CC(=CC(=C1O)OC)C=O

1 reference

SYRINGALDEHYDE (English)

7 October 2016

melting point

112.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

safety classification and labelling

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

NFPA Health

1

NFPA Fire

0

NFPA Instability

0

1 reference

imported from Wikimedia project

English Wikipedia

found in taxon

Pilocarpus grandiflorus

1 reference

A New Imidazole Alkaloid and Other Constituents from Pilocarpus grandiflorus and their Antifungal Activity

Zanthoxylum gilletii

1 reference

Constituents of Fagara macrophylla and Zanthoxylum rigidifolium Pericarps

Populus lasiocarpa

1 reference

Phenolic analysis of bud exudate of Populus lasiocarpa by GC/MS

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

Posidonia oceanica

1 reference

Distribution of phenolic compounds in the seagrass Posidonia oceanica

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†

Cinnamomum kotoense

2 references

Antitubercular constituents from the stem wood of Cinnamomum kotoense

Chemical and cytotoxic constituents from the leaves of Cinnamomum kotoense

Cinnamomum subavenium

4 references

Cytotoxic constituents from the leaves of Cinnamomum subavenium

Cytotoxic constituents of the stems of Cinnamomum subavenium

Cytotoxic constituents of the stems of Cinnamomum subavenium

A novel sesquiterpenoid from the leaves of Cinnamomum subavenium

Microtropis japonica

3 references

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

Antitubercular dihydroagarofuranoid sesquiterpenes from the roots of Microtropis fokienensis

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

Q15561302

2 references

Isolation of syringaldehyde from Mikania laevigata medicinal extract and its influence on the fatty acid profile of mice

New constituents from Mikania laevigata Shultz Bip. ex Baker

Zanthoxylum ailanthoides

6 references

Amides and Benzenoids from Zanthoxylum ailanthoides with Inhibitory Activity on Superoxide Generation and Elastase Release by Neutrophils

Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils

Chemical Constituents from the Root Bark of FormosanZanthoxylum Ailanthoides

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

Constituents of the root wood of Zanthoxylum wutaiense with antitubercular activity

New phenylpropenoids, bis(1-phenylethyl)phenols, bisquinolinone alkaloid, and anti-inflammatory constituents from Zanthoxylum integrifoliolum

Magnolia officinalis

1 reference

Phenolic constituents from the stem bark of Magnolia officinalis

Isatis tinctoria

2 references

A comprehensive metabolite profiling of Isatis tinctoria leaf extracts

A comprehensive metabolite profiling of Isatis tinctoria leaf extracts

Arabidopsis thaliana

2 references

Metabolomics-oriented isolation and structure elucidation of 37 compounds including two anthocyanins from Arabidopsis thaliana

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

Cissus sicyoides

1 reference

Structures of new flavonoids and benzofuran-type stilbene and degranulation inhibitors of rat basophilic leukemia cells from the Brazilian herbal medicine Cissus sicyoides

Zanthoxylum wutaiense

4 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

Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils

New phenylpropenoids, bis(1-phenylethyl)phenols, bisquinolinone alkaloid, and anti-inflammatory constituents from Zanthoxylum integrifoliolum

Annona montana

1 reference

Bioactive constitutents from the stems of Annona montana.

Tetradium glabrifolium

1 reference

The heartwood constituents of Tetradium glabrifolium

Aralia bipinnata

2 references

Lignans from the wood of Aralia bipinnata

Phenylpropanoids from Aralia bipinnata

Coriandrum sativum

1 reference

Three isocoumarins from Coriandrum sativum

Ilex rotunda

1 reference

A dimeric sinapaldehyde glucoside from Ilex rotunda

Clausena excavata

1 reference

Carbazole alkaloids from Clausena excavata and their biological activity

Rhinacanthus nasutus

3 references

Naphthoquinone esters from the root of Rhinacanthus nasutus

Rhinacanthin-Q, a naphthoquinone from Rhinacanthus nasutus and its biological activity

Rhinacanthin-Q, a naphthoquinone from Rhinacanthus nasutus and its biological activity

Brosimum acutifolium

1 reference

Flavonoids from Brosimum acutifolium

Gynura elliptica

1 reference

Anti-platelet aggregation constituents from Gynura elliptica

Magnolia sinica

1 reference

Chemical constituents of two Chinese Magnoliaceae plants, Tsoongiodendron odorum and Manglietiastrum sinicum, and their inhibition of platelet aggregation

Annona cherimola

1 reference

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

Boronia pinnata

3 references

CONSTITUENTS OF KIGELIA PINNATA

Constituents of Boronia pinnata

Constituents of Boronia pinnata

Hibiscus cannabinus

1 reference

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

Hydrangea chinensis

1 reference

Hydrachine A, a novel alkaloid from the roots of Hydrangea chinensis

Machilus obovatifolia

1 reference

Cytotoxic neolignans and butanolides from Machilus obovatifolia

Ficus septica

1 reference

Non-Alkaloidal Constituents from the Stem ofFicus Septica

Piper solmsianum

1 reference

Trypanocidal tetrahydrofuran lignans from inflorescences of Piper solmsianum

Casearia membranacea

1 reference

A cytotoxic butenolide, two new dolabellane diterpenoids, a chroman and a benzoquinol derivative formosan Casearia membranacea

Hibiscus taiwanensis

2 references

Constituents from the Stems of Hibiscus taiwanensis.

Constituents from the stems of Hibiscus taiwanensis.

Zanthoxylum nitidum

2 references

Studies on Xanthoxylun spp. II. Constituents of the bark of Xanthoxylum piperitum DC.

New benzenoids and anti-inflammatory constituents from Zanthoxylum nitidum

Rhizophora apiculata

1 reference

Long chain aliphatic alcohols and saturated carboxylic acids from heartwood of Rhizophora apiculata

Fagraea racemosa

1 reference

Pharmacologically active components of Todopon Puok (Fagraea racemosa), a medicinal plant from Borneo.

Gymnosporia pyria

1 reference

Use of COMPARE analysis to discover functional analogues of bleomycin

Phyllostachys nigra

1 reference

Inhibitors of cyclic adenosine 3',5'-monophosphate phosphodiesterase in Phyllostachys nigra MUNRO var. henonis STAPF. and Phragmites communis TRIN., and inhibition by related compounds

Mikania shushunensis

1 reference

Bisabolones and other constituents of Mikania shushunensis

Codonopsis pilosula

1 reference

Two New Triterpenoids from the Roots of Codonopsis pilosula.

Zanthoxylum integrifoliolum

5 references

New phenylpropenoids, bis(1-phenylethyl)phenols, bisquinolinone alkaloid, and anti-inflammatory constituents from Zanthoxylum integrifoliolum

Chemical Constituents from the Root Wood ofZanthoxylum Integrifoliolum

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

Constituents of the root wood of Zanthoxylum wutaiense with antitubercular activity

Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils

Daphne feddei

1 reference

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production

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

Juglans regia

1 reference

Phenolic acids, syringaldehyde, and juglone in fruits of different cultivars of Juglans regia L.

Senna

1 reference

Pharmacologically Active Phenylpropanoids fromSenra incana

Aframomum giganteum

1 reference

Dehydrozingerone from Aframomum giganteum

Gymnadenia conopsea

1 reference

Bioactive constituents from Chinese natural medicines. XVII. constituents with radical scavenging effect and new glucosyloxybenzyl 2-isobutylmalates from Gymnadenia conopsea

Taraxacum formosanum

2 references

Chemical constituents from roots of Taraxacum formosanum

Chemical constituents from roots of Taraxacum formosanum

Diplospora dubia

1 reference

Rearranged ent-kauranes from the stems of Tricalysia dubia and their biological activities

Vepris uguenensis

2 references

An azole, an amide and a limonoid from Vepris uguenensis (Rutaceae).

An azole, an amide and a limonoid from Vepris uguenensis (Rutaceae).

Viscum coloratum

2 references

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

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

Senra incana

1 reference

Pharmacologically Active Phenylpropanoids fromSenra incana

Vitis vinifera

1 reference

Separation of phenolic compounds by high-performance liquid chromatography with absorbance and fluorimetric detection.

Imperata cylindrica

1 reference

Chemical interaction in the invasiveness of cogongrass (Imperata cylindrica (L.) Beauv.).

Ambrosia cumanensis

1 reference

A sesquiterpenoid lactone from Ambrosia cumanensis

Ambrosia psilostachya

1 reference

A sesquiterpenoid lactone from Ambrosia cumanensis

Beta vulgaris

1 reference

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

Centaurea nicolai

1 reference

Guaianolides from Centaurea nicolai: antifungal activity

Diospyros maritima

1 reference

Chemical constituents from the stems of Diospyros maritima

Wikstroemia canescens

1 reference

Phenolic compounds from the aerial parts of Diplomorpha canescens

Corymbia citriodora

1 reference

The Chemical Constituents from the Heartwood ofEucalyptus Citriodora

Euphorbia lagascae

1 reference

Lagaspholones A and B: two new jatropholane-type diterpenes from Euphorbia lagascae

Eurycoma longifolia

1 reference

Cytotoxic and antimalarial constituents from the roots of Eurycoma longifolia

Fatoua pilosa

1 reference

A novel dimeric coumarin analog and antimycobacterial constituents from Fatoua pilosa

Fibraurea tinctoria

1 reference

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

Garcinia linii

1 reference

Benzopyrans, biphenyls and xanthones from the root of Garcinia linii and their activity against Mycobacterium tuberculosis

Gardenia carinata

1 reference

DNA topoisomerase IIα inhibitory and anti-HIV-1 flavones from leaves and twigs of Gardenia carinata

Strobilanthes psilostachys

1 reference

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

Laguncularia racemosa

1 reference

Phenolic compounds and their anti-oxidative properties and protein kinase inhibition from the Chinese mangrove plant Laguncularia racemosa

Licaria puchury-major

1 reference

Arylpropanoids from Licaria puchury-major

Lithospermum erythrorhizon

2 references

Measurement of Phenolic Compounds and Their Effect on Shikonin Production in Lithospermum Cultured Cells.

cDNA cloning and gene expression of phenylalanine ammonia-lyase in Lithospermum erythrorhizon.

Magnolia grandiflora

1 reference

Rare natural products from the wood of Magnolia grandiflora

Magnolia kachirachirai

1 reference

Cytotoxic sesquiterpenes from Magnolia kachirachirai

Melicope semecarpifolia

1 reference

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

Magnolia compressa

1 reference

Chemical constituents from the leaves of Michelia compressa var. formosana

Monascus purpureus

1 reference

Chemical constituents from the fungus Monascus purpureus and their antifungal activity

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

Picris rhagadioloides

1 reference

The first guaian-12-oic acid glucopyranosyl ester and other constituents from Picris rhagadioloides (L.) Desf. (Asteraceae).

Pisonia umbellifera

1 reference

Chemical constituents and antitubercular activity of Formosan Pisonia umbellifera

Platycarya strobilacea

1 reference

ent-Eudesmane sesquiterpenoids, galloyl esters of the oak lactone precursor, and a 3-O-methylellagic acid glycoside from the wood of Platycarya strobilacea

Premna tomentosa

2 references

New icetexane diterpenes with intestinal α-glucosidase inhibitory and free-radical scavenging activity isolated from Premna tomentosa roots

Bioactivity-guided isolation of cytotoxic constituents from stem-bark of Premna tomentosa

Brucea javanica

2 references

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

Stereospermum acuminatissimum

1 reference

Chemical constituents of Stereospermum acuminatissimum and their urease and α-chymotrypsin inhibitions.

Verbesina turbacensis

1 reference

Aromatic and other constituents of four Verbesina species: Structure and stereochemistry of verbesindiol

Boronia koniambiensis

1 reference

Koniamborine, the first pyrano[3,2-b]indole alkaloid and other secondary metabolites from Boronella koniambiensis

Moullava digyna

1 reference

Tarenna attenuata

1 reference

Tarennane and tarennone, two novel chalcone constituents from Tarenna attenuata

Aeschynanthus bracteatus

1 reference

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

Punica granatum

1 reference

Diverse Phytochemicals and Bioactivities in the Ancient Fruit and Modern Functional Food Pomegranate (Punica granatum).

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

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.

Libidibia ferrea

1 reference

Moullava tortuosa

1 reference

Caesalpinia bonducella

1 reference

Guilandina bonduc

1 reference

Pluchea indica

1 reference

Bioactive Constituents from the Aerial Parts of Pluchea indica Less

Orobanche variegata

1 reference

Phenolic metabolites from Orobanche speciosa

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.

Phaseolus vulgaris

2 references

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

Alpha-amylase, α-glucosidase and lipase inhibiting activities of polyphenol-rich extracts from six common bean cultivars of Southern Italy, before and after cooking.

basil

1 reference

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

Triticum aestivum

1 reference

Identification and quantitation of lipophilic extractives from wheat straw

Cissus discolor

1 reference

Structures of new flavonoids and benzofuran-type stilbene and degranulation inhibitors of rat basophilic leukemia cells from the Brazilian herbal medicine Cissus sicyoides

Taraxacum mongolicum

1 reference

Chemical constituents from roots of Taraxacum formosanum

Fatoua villosa

1 reference

A novel dimeric coumarin analog and antimycobacterial constituents from Fatoua pilosa

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

Syzygium sandwicense

1 reference

Constituents of Eugenia sandwicensis with potential cancer chemopreventive activity.

Strobilanthes pentstemonoides

1 reference

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

0 references

0 references

Syringaldehyde

0 references

Identifiers

InChI

InChI=1S/C9H10O4/c1-12-7-3-6(5-10)4-8(13-2)9(7)11/h3-5,11H,1-2H3

1 reference

SYRINGALDEHYDE (English)

KCDXJAYRVLXPFO-UHFFFAOYSA-N

7 October 2016

InChIKey

2 references

SYRINGALDEHYDE (English)

7 October 2016

ChEBI release 2020-09-01

2 references

syringaldehyde (English)

KCDXJAYRVLXPFO-UHFFFAOYSA-N

7 October 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=134-96-3

1 reference

Syringaldehyde (English)

7 October 2016

1 reference

SYRINGALDEHYDE (English)

7 October 2016

Reaxys registry number

784514

1 reference

syringaldehyde (English)

7 October 2016

ChEBI ID

67380

mapping relation type

1 reference

syringaldehyde (English)

7 October 2016

1 reference

splash10-002b-9500000000-648b4cea88c99f600180

SYRINGALDEHYDE (English)

7 October 2016

1 reference

inferred from InChIKey

1 reference

MassBank accession ID

MSBNK-RIKEN-PR100983

0 references

MSBNK-RIKEN-PR101041

0 references

MSBNK-IPB_Halle-PB000619

0 references

MSBNK-IPB_Halle-PB000620

0 references

MSBNK-IPB_Halle-PB000621

0 references

MSBNK-IPB_Halle-PB000622

0 references

SPLASH

0 references

splash10-004i-9100000000-54826f5ed4bf4c650678

0 references

splash10-00or-9000000000-03822b23e64682ed8879

0 references

splash10-0gb9-0900000000-371d26896933e850f066

0 references

splash10-0092-8900000000-d831c678224eb2d019b0

0 references

splash10-001i-0900000000-6bf494720d1f63491abc

0 references

splash10-00di-2900000000-fe030c384ccd6b3e81d4

0 references

splash10-002e-9300000000-212b73e3eac8b940a2d1

0 references

splash10-004i-9100000000-e3b60bb3294f2b0fe32e

0 references

splash10-001i-0900000000-4612efe24789ea29a79b

0 references

splash10-00di-2900000000-dc20f0af8c82cefac43b

0 references

splash10-004i-9400000000-2dbec98af26a584baa68

0 references

RTECS number

CU5760000

1 reference

imported from Wikimedia project

1 reference

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

DSSTOX compound identifier

0 references

0 references

205-167-5

1 reference

Global Substance Registration System

UNII

2ZR01KTT21

SYRINGALDEHYDE (English)

ECHA Substance Infocard ID

7 October 2016

100.004.698

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.004.698

27 December 2018

AICS Chemical ID (BEING DELETED)

4-hydroxy-3,5-dimethoxybenzaldehyde (English)

quotation

CAS no.: 134-96-3 (English)

FL number

05.153

1 reference

quotation

CAS no.: 134-96-3 (English)

23 January 2021

05.153

3763

0 references

Human Metabolome Database ID

HMDB0258653

1 reference

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00007558

1 reference

based on heuristic

inferred from InChIKey

UNII

2ZR01KTT21

1 reference

Global Substance Registration System

UNII

2ZR01KTT21

SYRINGALDEHYDE (English)

7 October 2016

0 references

1 reference

28 October 2013

1878

1 reference

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