dihydroferulic acid (Q10395564)

1135-23-5 (English)

14 October 2016

C₁₀H₁₂O₄

1 reference

1135-23-5 (English)

14 October 2016

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

1 reference

1135-23-5 (English)

14 October 2016

90.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Bulbophyllum vaginatum

1 reference

Phenanthrene and other aromatic constituents of Bulbophyllum vaginatum

Colchicum kotschyi

1 reference

Alkaloids and phenolics of Colchicum turcicum

Dianthus superbus

1 reference

Longicalycinin A, a New Cytotoxic Cyclic Peptide from Dianthus superbus var. longicalycinus (Maxim.) Will.

Ailanthus altissima

1 reference

Triterpenoids and Sterones from the Stem Bark of Ailanthus altissima

Melicope semecarpifolia

1 reference

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

Picea glauca

1 reference

Comparison of phenolic compounds from galls and shoots of Picea glauca

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.

Zingiber officinale

2 references

Two new phenylalkanoids from the rhizomes of Zingiber officinale

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.

Malva sylvestris

1 reference

Terpenoids and phenol derivatives from Malva silvestris

Curcuma longa

1 reference

Metabolite analysis in Curcuma domestica using various GC-MS and LC-MS separation and detection techniques

Stauntonia hexaphylla

1 reference

Bioactive triterpene glycosides from the fruit of Stauntonia hexaphylla and insights into the molecular mechanism of its inflammatory effects

Identifiers

InChI

InChI=1S/C10H12O4/c1-14-9-6-7(2-4-8(9)11)3-5-10(12)13/h2,4,6,11H,3,5H2,1H3,(H,12,13)

1 reference

1135-23-5 (English)

14 October 2016

2 references

1135-23-5 (English)

14 October 2016

ChEBI release 2020-09-01

CAS Registry Number

1135-23-5

2 references

Global Substance Registration System

dihydroferulic acid (English)

14 October 2016

https://commonchemistry.cas.org/detail?cas_rn=1135-23-5

8 April 2021

1 reference

3-(4-Hydroxy-3-methoxyphenyl)propanoic acid (English)

14 October 2016

2 references

1135-23-5 (English)

14 October 2016

ChEBI ID

86612

mapping relation type

exact match

2 references

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C10H12O4/c1-14-9-6-7(2-4-8(9)11)3-5-10(12)13/h2,4,6,11H,3,5H2,1H3,(H,12,13)

1 reference

DIHYDROFERULIC ACID (English)

14 October 2016

2 references

inferred from InChIKey

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

1 reference

2 references

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

dihydroferulic acid (English)

ECHA Substance Infocard ID

14 October 2016

100.013.172

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.013.172

27 December 2018

Human Metabolome Database ID

3-(4-hydroxy-3-methoxyphenyl)propionic acid (English)

quotation

CAS no.: 1135-23-5 (English)

HMDB0062121

2 references

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00040946

2 references

based on heuristic

inferred from InChIKey

2 references

Global Substance Registration System

dihydroferulic acid (English)

14 October 2016