(Q411602)

3,4-Dihydroxybenzaldehyde (English)

6 October 2016

chemical formula

C₇H₆O₃

1 reference

3,4-Dihydroxybenzaldehyde (English)

19 November 2016

canonical SMILES

C1=CC(=C(C=C1C=O)O)O

1 reference

3,4-Dihydroxybenzaldehyde (English)

19 November 2016

melting point

155 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Populus simonii

1 reference

Notes: Analysis of Phenolics of Bud Exudates of Populus simonii and Populus yunnanensis by GC-MS

Populus ciliata

1 reference

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

Populus tristis

1 reference

Analysis of Phenolics of Bud Exudate of Populus tristis by GC/MS

Populus violascens

1 reference

Notes: Analysis of Phenolics of Bud Exudate of Populus violascens by GC-MS

Actaea racemosa

3 references

Polyphenolic constituents of Actaea racemosa

Polyphenolic Constituents of Actaea racemosa

Analysis of formononetin from black cohosh (Actaea racemosa).

Bletilla formosana

1 reference

Dihydrophenanthrenes from Bletilla formosana

Cryptotympana

1 reference

Optically active N-acetyldopamine dimer of the crude drug "Zentai," the cast-off shell of the Cicada, Cryptotympana sp.

Hordeum vulgare

1 reference

3,4-dihydroxybenzaldehyde purified from the barley seeds (Hordeum vulgare) inhibits oxidative DNA damage and apoptosis via its antioxidant activity

Inonotus obliquus

2 references

Antioxidant Small Phenolic Ingredients in Inonotus obliquus (persoon) Pilat (Chaga)

Chemical constituents from Inonotus obliquus and their biological activities

Phellinus igniarius

1 reference

Phelligridins C-F: cytotoxic pyrano[4,3-c][2]benzopyran-1,6-dione and furo[3,2-c]pyran-4-one derivatives from the fungus Phellinus igniarius

Posidonia oceanica

1 reference

Distribution of phenolic compounds in the seagrass Posidonia oceanica

Streptomyces lincolnensis

2 references

Rancinamycins, metabolites produced by Streptomyces lincolnensis in sulfur-depleted media

New Rancinamycin Analogues from Streptomyces lincolnensis

Haplopteris anguste-elongata

1 reference

Constituents of Vittaria anguste-elongata and their biological activities

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.

black cardamom

1 reference

1,1-Diphenyl-2-picrylhydrazyl radical-scavenging active compounds from greater cardamom (Amomum subulatum Roxb.).

Artemisia sacrorum

1 reference

Chemical constituents from Artemisia annua

Calophyllum macrocarpum

1 reference

Xanthones and neoflavonoids from two asian species of calophyllum

Magnolia crassipes

1 reference

Phenolic constituents from Oplopanax horridus

Odontosoria gymnogrammoides

1 reference

Chemical and Chemotaxonomical Studies of Filices. LXXII. Chemical Studies on the Constituents of Odontosoria gymnogrammoides CHRIST

Populus euphratica

1 reference

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

Pyrrosia petiolosa

1 reference

Chemical constituents of Pyrrosia petiolosa

Quercus suber

2 references

Low Molecular Weight Polyphenols in Cork ofQuercus suber

Polyphenolic Composition ofQuercus suberCork from Different Spanish Provenances

Salvia chinensis

3 references

Isosalvianolic acid C, a depside possessing a dibenzooxepin skeleton

Isosalvianolic acid C, a depside possessing a dibenzooxepin skeleton

Isosalvianolic acid C, a depside possessing a dibenzooxepin skeleton

Salvia miltiorrhiza

7 references

Determination of β-(3,4-dihydroxyphenyl) lactic acid, protocatechuic acid and protocatechuic aldehyde in radixSalviae Miltiorrhizae by capillary electrophoresis

Quantitative analysis of the marker compounds in Salvia miltiorrihiza root and its phytomedicinal preparations

Simultaneous Determination of Rosmarinic Acid, Lithospermic Acid B, and Related Phenolics inSalvia miltiorrhizaby HPLC

Separation and determination of protocatechuic aldehyde and protocatechuic acid in Salivia miltorrhrza by capillary electrophoresis with amperometric detection

Simultaneous detection of seven phenolic acids in Danshen injection using HPLC with ultraviolet detector

Interaction of salvianolic acids and notoginsengnosides in inhibition of ADP-induced platelet aggregation

Potency fingerprint of herbal products Danshen injection for their quality evaluation.

Salvia przewalskii

1 reference

Polyphenolic constituents of Actaea racemosa

Virola multinervia

1 reference

Lignans and benzoic acid derivatives from pericarps of Virola multinervia (Myristicaceae)

Visnea mocanera

1 reference

Phenolic Composition of the “Mocán” (VisneamocaneraL.f.)

Vitis vinifera

2 references

Extraction of Natural Complex Phenols and Tannins from Grape Seeds by Using Supercritical Mixtures of Carbon Dioxide and Alcohol

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

Cullen corylifolia

1 reference

Bioactive Metabolites from the Fruits of Psoralea corylifolia

Cullen corylifolium

1 reference

Bioactive Metabolites from the Fruits of Psoralea corylifolia

Centipeda minima

1 reference

Antioxidant and anti-inflammatory activities of aqueous extract of Centipeda minima

Amorphophallus konjac

1 reference

Peroxynitrite scavenging activities of aromatic compounds isolated from Konnyaku, Amorphophallus konjac K.Koch

Aster himalaicus

1 reference

Eudesmane sesquiterpenes and other constituents from Aster himalaicus

Beta vulgaris

1 reference

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

Dryopteris crassirhizoma

1 reference

Two new triterpenes from the Rhizome of Dryopteris crassirhizoma, and inhibitory activities of its constituents on human immunodeficiency virus-1 protease

Fagopyrum esculentum

1 reference

Antioxidant Compounds from Buckwheat (Fagopyrum esculentumMöench) Hulls

Ganoderma applanatum

1 reference

Aldose reductase inhibitors from the fruiting bodies of Ganoderma applanatum

Hydnophytum formicarum

1 reference

Antimicrobial and antioxidative activities of bioactive constituents from Hydnophytum formicarum Jack.

Hymenochaete xerantica

1 reference

Free radical scavengers from the medicinal mushroom Inonotus xeranticus and their proposed biogenesis

Duhaldea cappa

1 reference

Chemical constituents from Inula cappa

Joannesia princeps

1 reference

Joannesialactone and other compounds from Joannesia princeps

Collinsonia japonica

1 reference

Hyaluronidase inhibitors from Keiskea japonica

Menispermum dauricum

1 reference

Isoquinoline and isoindole alkaloids from Menispermum dauricum

Perilla frutescens

2 references

Two Jasmonoid Glucosides and a Phenylvaleric Acid Glucoside fromPerilla frutescens

Novel Antioxidants Isolated from Perilla frutescens Britton var. crispa (Thunb.).

Ipomoea nil

1 reference

Bioactive phenolic constituents from the seeds of Pharbitis nil.

Polyporus umbellatus

1 reference

Studies on active substances in herbs used for hair treatment. I. Effects of herb extracts on hair growth and isolation of an active substance from Polyporus umbellatus F

Ranunculus sceleratus

1 reference

Evaluation of antiviral activity of compounds isolated from Ranunculus sieboldii and Ranunculus sceleratus

Salsola collina

1 reference

Chemical and biologically active constituents of Salsola collina

Salvia divinorum

2 references

Neo-clerodane diterpenes from the hallucinogenic sage Salvia divinorum

Neo-clerodane Diterpenes from the Hallucinogenic SageSalvia divinorum.

Inonotus hispidus

1 reference

Antioxidant hispidin derivatives from medicinal mushroom Inonotus hispidus

Salvia prionitis

1 reference

Quantitative analysis of the marker compounds in Salvia miltiorrihiza root and its phytomedicinal preparations

Annona cornifolia

1 reference

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

Salvia syriaca

1 reference

Quantitative analysis of the marker compounds in Salvia miltiorrihiza root and its phytomedicinal preparations

Garcinia scortechinii

1 reference

Constituents of the pericarp of Garcinia subelliptica

Garcinia acuminata

1 reference

Constituents of the pericarp of Garcinia subelliptica

Salvia trijuga

1 reference

Quantitative analysis of the marker compounds in Salvia miltiorrihiza root and its phytomedicinal preparations

Garcinia elliptica

1 reference

Constituents of the pericarp of Garcinia subelliptica

Picea jezoensis

1 reference

Structures and radical-scavenging activities of phenolic constituents from the bark of Picea jezoensis var. jezoensis

Macrohyporia cocos

1 reference

Bioactivity-guided isolation of anti-inflammatory triterpenoids from the sclerotia of Poria cocos using LPS-stimulated Raw264.7 cells

Wolfiporia cocos

1 reference

Bioactivity-guided isolation of anti-inflammatory triterpenoids from the sclerotia of Poria cocos using LPS-stimulated Raw264.7 cells

Lanxangia tsao-ko

1 reference

Constituents of Amomum tsao-ko and their radical scavenging and antioxidant activities

Pluchea indica

1 reference

Bioactive Constituents from the Aerial Parts of Pluchea indica Less

Senna garrettiana

1 reference

Chemical studies on the heartwood of Cassia garrettiana Craib. II. Nonanthraquinonic constituents.

Houttuynia cordata

1 reference

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

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

Picea abies

1 reference

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

Capsicum annuum

1 reference

Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in pepper fruit (Capsicum annuum L.).

Artemisia gmelinii

1 reference

Chemical constituents from Artemisia annua

Tropicoporus linteus

3 references

A sphingolipid and tyrosinase inhibitors from the fruiting body of Phellinus linteus

Inhibitory constituents of aldose reductase in the fruiting body of Phellinus linteus.

Protein glycation inhibitors from the fruiting body of Phellinus linteus

Chrysanthemum morifolium

1 reference

Xanthine oxidase inhibitors from the flowers of Chrysanthemum sinense

Populus szechuanica

1 reference

Notes: Analysis of Phenolics of Bud Exudate of Populus violascens by GC-MS

Garcinia ovalifolia

1 reference

Constituents of the pericarp of Garcinia subelliptica

Garcinia dulcis

1 reference

Constituents of the pericarp of Garcinia subelliptica

Populus trichocarpa

1 reference

Analysis of Phenolics of Bud Exudate of Populus tristis by GC/MS

Vertebrata lanosa

1 reference

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

subject has role

anticoagulant

1 reference

InChI=1S/C7H6O3/c8-4-5-1-2-6(9)7(10)3-5/h1-4,9-10H

Medical Subject Headings

15 March 2018

Protocatechuic aldehyde

0 references

Identifiers

InChI

1 reference

3,4-Dihydroxybenzaldehyde (English)

19 November 2016

2 references

3,4-Dihydroxybenzaldehyde (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

139-85-5

2 references

protocatechualdehyde (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=139-85-5

10 April 2021

1 reference

Protocatechuic aldehyde (English)

19 November 2016

2 references

3,4-Dihydroxybenzaldehyde (English)

19 November 2016

Reaxys registry number

774381

1 reference

3,4-dihydroxybenzaldehyde (English)

6 October 2016

Gmelin number

123001

0 references

ChEBI ID

50205

mapping relation type

2 references

PROTOCATECHUALDEHYDE (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C7H6O3/c8-4-5-1-2-6(9)7(10)3-5/h1-4,9-10H

1 reference

PROTOCATECHUALDEHYDE (English)

19 November 2016

2 references

inferred from InChIKey

splash10-000i-0900000000-25b5b2bc87af9df04e91

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

splash10-000i-0900000000-03d9e2dbe57c9bcfb9ab

0 references

splash10-002r-0905000000-7987816fb8648b0eea18

0 references

splash10-0002-0040900010-522c055741661bbc5ba8

0 references

NMRShiftDB structure ID

20112325

1 reference

DSSTox substance ID

DTXSID4074512

2 references

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

DSSTOX compound identifier

0 references

0 references

1 reference

protocatechualdehyde (English)

ECHA Substance Infocard ID

19 November 2016

100.004.889

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.004.889

27 December 2018

imported from Wikimedia project

3,4-dihydroxybenzaldehyde (English)

quotation

CAS no.: 139-85-5 (English)

FL number

05.142

1 reference

quotation

CAS no.: 139-85-5 (English)

23 January 2021

05.142

1 reference

28 December 2019

PROTOCATECHUICALDEHYDE (English)

quotation

CAS no.: 139-85-5 (English)

1 reference

1 reference

1 reference

Medical Subject Headings

14 March 2018

1 reference

protocatechualdehyde (English)

19 November 2016

DrugBank ID

DB11268

1 reference

Human Metabolome Database ID

HMDB0059965

2 references

based on heuristic

inferred from InChIKey

3 references

3,4-dihydroxybenzaldehyde (English)

6 October 2016

based on heuristic

inferred from InChIKey

2 references

protocatechualdehyde (English)

19 November 2016

0 references

1 reference

1 reference