(Q414606)

5-HYDROXYMETHYLFURFURAL (English)

19 October 2016

chemical formula

C₆H₆O₃

1 reference

5-HYDROXYMETHYLFURFURAL (English)

19 November 2016

canonical SMILES

C1=C(OC(=C1)C=O)CO

1 reference

5-HYDROXYMETHYLFURFURAL (English)

19 November 2016

melting point

34 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Verruculina enalia

1 reference

The metabolites of the mangrove fungus Verruculina enalia No. 2606 from a salt lake in the Bahamas

Hydrastis canadensis

1 reference

Antioxidants in medicinal plant extracts. A research study of the antioxidant capacity of Crataegus, Hamamelis and Hydrastis

Tropicoporus linteus

1 reference

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

Aristolochia gehrtii

1 reference

Alkamides and phenethyl derivatives from Aristolochia gehrtii

Siphoneugena densiflora

1 reference

Enzymatic inhibitory activity and trypanocidal effects of extracts and compounds from Siphoneugena densiflora O. Berg and Vitex polygama Cham

Rehmannia glutinosa

2 references

Simultaneous analysis of furfural metabolites from Rehmanniae radix preparata by HPLC-DAD-ESI-MS.

Phytochemical Studies of Rehmannia glutinosa Rhizones

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.

Eleutherococcus senticosus

1 reference

A benzenoid from the stem of Acanthopanax senticosus

Anemarrhena asphodeloides

1 reference

On-line purity monitoring in high-speed counter-current chromatography: application of HSCCC-HPLC-DAD for the preparation of 5-HMF, neomangiferin and mangiferin from Anemarrhena asphodeloides Bunge

Dendrobium chrysanthum

1 reference

[Chemical constituents of Dendrobium candidum]

Vitis vinifera

1 reference

Separation and Identification of Furanic Compounds in Fruit Juices and Drinks by High-Performance Liquid Chromatography Photodiode Array Detection

Aralia bipinnata

2 references

Lignans from the wood of Aralia bipinnata

Phenylpropanoids from Aralia bipinnata

Clivia miniata

1 reference

Supercritical fluid extraction and analysis of compounds from Clivia miniata for uterotonic activity.

Allium cepa

1 reference

Isolation and identification of potential cancer chemopreventive agents from methanolic extracts of green onion (Allium cepa).

Pluchea sagittalis

1 reference

Natural products from Pluchea sagittalis act as inhibitors of photosynthesis in vitro.

Eucommia ulmoides

1 reference

Effects of Eucommia ulmoides Oliver leaf extract on 3T3-L1 differentiation into adipocytes

Gonocaryum calleryanum

1 reference

A secoiridoid and other constituents of Gonocaryum calleryanum

Gymnadenia conopsea

2 references

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

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

Monascus pilosus

2 references

Secondary metabolites from the mycelia of the fungus Monascus pilosus BCRC 38072.

Secondary metabolites from the mycelia of the fungus Monascus pilosus BCRC 38072.

Scrophularia ningpoensis

2 references

A sugar ester and an iridoid glycoside from Scrophularia ningpoensis

A sugar ester and an iridoid glycoside from Scrophularia ningpoensis

Chondrophycus undulatus

1 reference

In vitro antioxidant activity of 5-HMF isolated from marine red alga Laurencia undulata in free-radical-mediated oxidative systems

Aristolochia kaempferi

1 reference

Constituents from the stem and root of Aristolochia kaempferi

Bryothamnion triquetrum

1 reference

A 1H- and 13C-n.m.r. study of an agar polysaccharide from Bryothamnion triquestrum

Cassia fistula

1 reference

Four new compounds from the seeds of Cassia fistula

Acalypha spiciflora

1 reference

Clerodanes and other constituents of Cleidion spiciflorum

Cleistopholis glauca

1 reference

Novel oligorhamnosides from the stem bark of Cleistopholis glauca

Dorstenia excentrica

1 reference

Furocoumarins of three species of the genus Dorstenia

Garcinia subelliptica

1 reference

Constituents of the pericarp of Garcinia subelliptica

Gastrodia elata

3 references

Neuroprotective Principles fromGastrodiaelata

Two new benzofurans from Gastrodia elata and their DNA topoisomerases I and II inhibitory activities

Two New Phenolic Compounds from the Rhizomes of Gastrodia elataBlume

Hippophae rhamnoides

1 reference

Chemical constituents from the fruits of Hippophae rhamnoides

Hyoscyamus niger

2 references

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

Hyosmin, a New Lignan from Hyoscyamus Niger L

Duhaldea cappa

1 reference

Chemical constituents from Inula cappa

Peperomia leptostachya

1 reference

Chemical and cytotoxic constituents from Peperomia sui

Prunus mume

2 references

Mumefural, citric acid derivative improving blood fluidity from fruit-juice concentrate of Japanese apricot (Prunus mume Sieb. et Zucc)

The screening of Chinese crude drugs for Ca2+ antagonist activity: identification of active principles from the aerial part of Pogostemon cablin and the fruits of Prunus mume

Saussurea cordifolia

1 reference

Chemical constituents from Saussurea cordifolia

Talaromyces flavus

1 reference

The metabolites of Talaromycesflavus: Part 1. Metabolites of the organic extracts

Xanthium strumarium

1 reference

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

Alsidium triquetrum

1 reference

A 1H- and 13C-n.m.r. study of an agar polysaccharide from Bryothamnion triquestrum

Tussilago farfara

1 reference

Sesquiterpenoids and other constituents from the flower buds of Tussilago farfara

Equisetum debile

1 reference

Chemical constituents of Equisetum debile

Polyporus umbellatus

1 reference

1β-hydroxylfriedelin, a new natural pentacylic triterpene from the sclerotia of <I>Polyporus umbellatus</I>

Scrophularia buergeriana

1 reference

A sugar ester and an iridoid glycoside from Scrophularia ningpoensis

Disporopsis

1 reference

Homoisoflavanones from Disporopsis aspera

Planochloris

1 reference

Homoisoflavanones from Disporopsis aspera

Scrophularia nodosa

1 reference

A sugar ester and an iridoid glycoside from Scrophularia ningpoensis

Foeniculum vulgare

1 reference

Effect of boiling and roasting on the polyacetylene and polyphenol content of fennel (Foeniculum vulgare) bulb

Carica papaya

1 reference

A new aliphatic ester of hydroxysalicylic acid from fermented Carica papaya L. preparation with a potential hair growth stimulating activity

Cornus officinalis

3 references

A Rapid and Sensitive Assay for Determining the Main Components in Processed Fructus Corni by UPLC–Q-TOF-MS

Simultaneous Determination of 11 High-Polarity Components from Fructus Corni: A Quantitative LC-MS/MS Method for Improved Quality Control.

Rapid simultaneous identification and determination of the multiple compounds in crude Fructus Corni and its processed products by HPLC-MS/MS with multiple reaction monitoring mode

Picea abies

1 reference

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

Houttuynia cordata

1 reference

Gas chromatography–mass spectrometry analysis of volatile compounds from Houttuynia cordata Thunb after extraction by solid-phase microextraction, flash evaporation and steam distillation

Nicotiana tabacum

1 reference

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

Eucalyptus leucoxylon

1 reference

Composition of Australian Honey Extractives. 1. Norisoprenoids, Monoterpenes, and Other Natural Volatiles from Blue Gum (Eucalyptus leucoxylon) and Yellow Box (Eucalyptus melliodora) Honeys

Eucalyptus melliodora

1 reference

Composition of Australian Honey Extractives. 1. Norisoprenoids, Monoterpenes, and Other Natural Volatiles from Blue Gum (Eucalyptus leucoxylon) and Yellow Box (Eucalyptus melliodora) Honeys

Peperomia humilis

1 reference

Chemical and cytotoxic constituents from Peperomia sui

0 references

0 references

Hydroxymethylfurfural

0 references

Identifiers

InChI

InChI=1S/C6H6O3/c7-3-5-1-2-6(4-8)9-5/h1-3,8H,4H2

1 reference

5-HYDROXYMETHYLFURFURAL (English)

NOEGNKMFWQHSLB-UHFFFAOYSA-N

19 November 2016

InChIKey

2 references

5-HYDROXYMETHYLFURFURAL (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

67-47-0

2 references

Global Substance Registration System

5-(hydroxymethyl)-2-furaldehyde (English)

NOEGNKMFWQHSLB-UHFFFAOYSA-N

19 November 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=67-47-0

1 reference

5-(Hydroxymethyl)-2-furaldehyde (English)

19 November 2016

1 reference

5-HYDROXYMETHYLFURFURAL (English)

19 November 2016

Reaxys registry number

110889

1 reference

5-hydroxymethylfurfural (English)

19 October 2016

Gmelin number

278693

0 references

ChEBI ID

412516

mapping relation type

1 reference

5-HYDROXYMETHYL-FURFURAL (English)

19 November 2016

2 references

5-HYDROXYMETHYL-FURFURAL (English)

19 November 2016

IUPHAR/BPS Guide to PHARMACOLOGY

8 February 2021

1 reference

MassBank accession ID

MSBNK-Fac_Eng_Univ_Tokyo-JP008160

0 references

SPLASH

splash10-004m-9200000000-81a66ec57fd350962398

0 references

splash10-000i-3900000000-55ebf60a0b891ce8f161

0 references

RTECS number

LT7031100

1 reference

imported from Wikimedia project

1 reference

Hazardous Substances Data Bank

28 October 2019

5-Hydroxymethyl-2-furfuraldehyde (English)

10 May 2021

1 reference

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

DSSTOX compound identifier

0 references

0 references

200-654-9

1 reference

Global Substance Registration System

5-(hydroxymethyl)-2-furaldehyde (English)

ECHA Substance Infocard ID

19 November 2016

100.000.595

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.000.595

27 December 2018

AICS Chemical ID (BEING DELETED)

5-(hydroxymethyl)-2-furaldehyde (English)

quotation

CAS no.: 67-47-0 (English)

FL number

13.139

1 reference

quotation

CAS no.: 67-47-0 (English)

23 January 2021

13.139

752

0 references

Guide to Pharmacology Ligand ID

10939

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

5 February 2021

1 reference

Human Metabolome Database ID

5-(hydroxymethyl)-2-furaldehyde (English)

publication date

3 July 2018

HMDB0034355

1 reference

based on heuristic

inferred from InChIKey

2 references

5-hydroxymethylfurfural (English)

19 October 2016

based on heuristic

inferred from InChIKey

1 reference

Global Substance Registration System

5-(hydroxymethyl)-2-furaldehyde (English)

19 November 2016

Natural Product Atlas ID

NPA000322

1 reference

based on heuristic

inferred from InChIKey

0 references

1 reference

Immune Epitope Database and Analysis Resource

5-hydroxymethylfurfural (English)

19 October 2016

1 reference

1 March 2022

0 references

1 reference

28 October 2013

Microsoft Academic ID

0 references

1 reference

26 January 2022

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

1 reference

26 January 2022

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

1 reference

1QXE (English)