isovanillin (Q412986)

German Wikipedia

mass

152.047 dalton

1 reference

3-Hydroxy-4-methoxybenzaldehyde (English)

14 October 2016

chemical formula

C₈H₈O₃

1 reference

3-Hydroxy-4-methoxybenzaldehyde (English)

14 October 2016

canonical SMILES

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

1 reference

3-Hydroxy-4-methoxybenzaldehyde (English)

14 October 2016

melting point

114 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Populus deltoides

1 reference

Chromatographic and chemometric investigation of the chemical defence mechanism of poplar tree genotypes against a bark fungine parasite

Bowdichia virgilioides

1 reference

Homoormosanine-type alkaloids from Bowdichia virgiloides

Pseudolarix amabilis

1 reference

Chemical constituents of Pseudolarix kaempferi Gord

Larix kaempferi

1 reference

Chemical constituents of Pseudolarix kaempferi Gord

Eleutherococcus senticosus

2 references

A benzenoid from the stem of Acanthopanax senticosus

Active components from Siberian ginseng (Eleutherococcus senticosus) for protection of amyloid β(25-35)-induced neuritic atrophy in cultured rat cortical neurons

Heteroplexis microcephala

1 reference

Chemical constituents of Heteroplexis micocephala.

Hemidesmus indicus

1 reference

Terpenoids from Hemidesmus indicus

Annona purpurea

3 references

New alkaloids from Annona purpurea

Four alkaloids from Annona cherimola.

Antiplatelet aggregation constituents from Annona purpurea

Cassytha filiformis

1 reference

Chemical constituents from Cassytha filiformis II

Neolitsea acuminatissima

1 reference

Cytotoxic constituents of the stem bark of Neolitsea acuminatissima

Tachigali paniculata

1 reference

Antioxidant and free-radical scavenging activity of constituents of the leaves of Tachigalia paniculata

Thalictrum przewalskii

1 reference

Thalprzewalskiinone, a new oxobenzylisoquinoline alkaloid from thalictrum przewalskii

Annona cherimola

3 references

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

Antiplatelet aggregation constituents from Annona purpurea

New alkaloids from Annona purpurea

Asparagus dumosus

1 reference

Chemical constituents from Asparagus dumosus

Ficus erecta var. beecheyana

1 reference

New Prenylated Flavones from the Roots ofFicus Beecheyana

Hernandia sonora

1 reference

Alkaloids from Hernandia sonora

Ligusticum porteri

2 references

Phthalides and Monoterpenes of the Hexane Extract of the Roots of Ligusticum porteri1

Phthalides and other constituents from Ligusticum porteri; sedative and spasmolytic activities of some natural products and derivatives

Mondia whitei

2 references

A chlorinated coumarinolignan from the African medicinal plant, Mondia whitei

Isolation of Isovanillin from Aromatic Roots of the Medicinal African Liane,Mondia whitei

Sphallerocarpus gracilis

1 reference

Two new quinones from Spallerocarpus gracillis

Ajania fruticulosa

1 reference

Biological and phytochemical investigations on Ajania fruticulosa

Carya cathayensis

1 reference

New antitumor compounds from Carya cathayensis

Vincetoxicum hemsleyanum

2 references

Chemical Constituents from the Roots of Morinda officinalis

Chemical constituents from the roots of Biondia chinensis

Securidaca diversifolia

1 reference

Benzophenones from the roots of the Popoluca Amerindian medicinal plant Securidaca diversifolia (L.) S.F. Blake

Orobanche crenata

1 reference

Phenolic metabolites from Orobanche speciosa

Orobanche variegata

1 reference

Phenolic metabolites from Orobanche speciosa

Valeriana officinalis

1 reference

Phenolic Compounds from the Roots of Valeriana officinalis var. latifolia

Zingiber officinale

1 reference

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.

Barbados nut

1 reference

Chemical constituents from leaves of Jatropha curcas

subject has role

enzyme inhibitor

1 reference

Medical Subject Headings

MeSH descriptor ID

C093382

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

15 March 2018

Identifiers

InChI

1 reference

3-Hydroxy-4-methoxybenzaldehyde (English)

14 October 2016

1 reference

Global Substance Registration System

3-Hydroxy-4-methoxybenzaldehyde (English)

14 October 2016

2 references

isovanillin (English)

14 October 2016

https://commonchemistry.cas.org/detail?cas_rn=621-59-0

8 April 2021

1 reference

Isovanillin (English)

14 October 2016

1 reference

3-Hydroxy-4-methoxybenzaldehyde (English)

14 October 2016

Reaxys registry number

1073021

1 reference

matched by identifier from

English Wikipedia

ChEBI ID

193161

mapping relation type

exact match

1 reference

International Chemical Identifier

InChI

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

1 reference

matched by identifier from

ISOVANILLIN (English)

14 October 2016

2 references

inferred from InChIKey

MSBNK-Fac_Eng_Univ_Tokyo-JP010304

1 reference

MassBank accession ID

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP010729

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP008445

0 references

SPLASH

splash10-0udi-9700000000-26471c62326769b48035

0 references

splash10-0udi-1900000000-0e2b8f2dc340d6296a83

0 references

RTECS number

CU6540000

1 reference

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

1 reference

DSSTOX compound identifier

0 references

0 references

210-694-9

1 reference

Global Substance Registration System

isovanillin (English)

ECHA Substance Infocard ID

14 October 2016

100.009.724

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.009.724

27 December 2018

3-hydroxy-p-anisaldehyde (English)

quotation

CAS no.: 621-59-0 (English)

MeSH descriptor ID

C093382

1 reference

matched by identifier from

Medical Subject Headings

14 March 2018

2 references

inferred from InChIKey

1 reference

Global Substance Registration System

isovanillin (English)

14 October 2016

0 references

1 reference

28 October 2013

Microsoft Academic ID

2776284534

0 references

Nikkaji ID

J57.879G

1 reference

https://ja.wikipedia.org/w/index.php?title=イソバニリン&oldid=67630336

Japanese Wikipedia

Wikimedia import URL

UMLS CUI

C0970873

1 reference

WikiUMLS: Aligning UMLS to Wikipedia via Cross-lingual Neural Ranking

C0297130

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023