orsellinic acid (Q414421)

participant

1 reference

Gene Ontology release 2019-11-16

o-orsellinic acid catabolic process

reactant

1 reference

Gene Ontology release 2019-11-16

o-orsellinic acid biosynthetic process

product

1 reference

Gene Ontology release 2019-11-16

chemical structure

Orsellinic acid.png
1,288 × 1,518; 20 KB

1 reference

imported from Wikimedia project

German Wikipedia

mass

168.042 dalton

1 reference

2,4-Dihydroxy-6-methylbenzoic acid (English)

19 October 2016

chemical formula

C₈H₈O₄

1 reference

2,4-Dihydroxy-6-methylbenzoic acid (English)

18 November 2016

canonical SMILES

CC1=CC(=CC(=C1C(=O)O)O)O

1 reference

Globosumones A-C, cytotoxic orsellinic acid esters from the Sonoran desert endophytic fungus Chaetomium globosum

2,4-Dihydroxy-6-methylbenzoic acid (English)

18 November 2016

1 reference

Stachybotrys cylindrospora

1 reference

Secondary metabolites of the aspen fungus Stachybotrys cylindrospora

Hypoxylon rubiginosum

1 reference

New azaphilones from the inedible mushroom Hypoxylon rubiginosum

Aspergillus terreus

2 references

Inducing secondary metabolite production by the soil-dwelling fungus Aspergillus terreus through bacterial co-culture

The isolation of 2,4-dihydroxy-3,6-dimethylbenzoic acid (3-methylorsellinic acid) from a culture of Aspergillus terreus

Cetrelia cetrarioides

1 reference

Chemical Constituents of Salvia frigida Boiss

Nidularia pulvinata

1 reference

Pulvinatal, a novel bioactive metabolite from the basidiomycete Nidularia pulvinata (Schw.) Fr

Parmelia tinctoria

1 reference

Chemical constituents from Paris mairei

Parmotrema stuppeum

1 reference

Phenolic constituents from the lichen Parmotrema stuppeum (Nyl.) Hale and their antioxidant activity

Stachybotrys cylindrosporus

1 reference

Secondary metabolites of the aspen fungus Stachybotrys cylindrospora

Umbilicaria torrefacta

1 reference

Applications of negative fast atom bombardment and MS/MS to screening of lichen compounds

Penicillium purpurogenum

2 references

Anti-influenza virus polyketides from the acid-tolerant fungus Penicillium purpurogenum JS03-21.

Studies in the biochemistry of micro-organisms. 110. Production and biosynthesis of orsellinic acid by Penicillium madriti G. Smith

Aspergillus fumigatus

3 references

Studies on the biosynthesis of quinones in fungi. Incorporation of 6-methylsalicylic acid into fumigatin and related compounds in Aspergillus fumigatus I.M.I. 89353.

Studies on the biosynthesis of phenols in fungi. Conversion of [14C]orsellinic acid and [14C]orcinol into fumigatol by Aspergillus fumigatus I.M.I. 89353

Metabolomics ofAspergillus fumigatus

Parmotrema cooperi

1 reference

New antiglycation and enzyme inhibitors from Parmotrema cooperi

Penicillium aurantiogriseum

1 reference

Stereospecific elimination of hydrogen atoms with opposite absolute orientations during the biosynthesis of orsellinic acid from chiral malonates in Penicillium cyclopium

Penicillium cyclopium

1 reference

Stereospecific elimination of hydrogen atoms with opposite absolute orientations during the biosynthesis of orsellinic acid from chiral malonates in Penicillium cyclopium

Aspergillus nidulans

1 reference

Intimate bacterial-fungal interaction triggers biosynthesis of archetypal polyketides in Aspergillus nidulans

Escherichia coli

1 reference

Intimate bacterial-fungal interaction triggers biosynthesis of archetypal polyketides in Aspergillus nidulans

Aspergillus flavus

1 reference

Molecular cloning and expression of the gene encoding a phospholipase A1 from Aspergillus oryzae

Parmotrema tinctorum

1 reference

Chemical constituents from Paris mairei

Dolichousnea longissima

1 reference

Lichen acids, plant growth inhibitors from Usnea longissima

Penicillium

1 reference

Polyketides with α-Glucosidase Inhibitory Activity from a Mangrove Endophytic Fungus, Penicillium sp. HN29-3B1.

antifungal

1 reference

A review of the potential of lichen substances as antifungal agents: the effects of extracts and lichen secondary metabolites on Fusarium fungi

Commons category

Orsellinic acid

0 references

Identifiers

InChI

InChI=1S/C8H8O4/c1-4-2-5(9)3-6(10)7(4)8(11)12/h2-3,9-10H,1H3,(H,11,12)

1 reference

2,4-Dihydroxy-6-methylbenzoic acid (English)

18 November 2016

2 references

2,4-Dihydroxy-6-methylbenzoic acid (English)

18 November 2016

ChEBI release 2020-09-01

CAS Registry Number

480-64-8

2 references

Global Substance Registration System

UNII

11XLA0494B

orsellinic acid (English)

18 November 2016

https://commonchemistry.cas.org/detail?cas_rn=480-64-8

10 April 2021

1 reference

Orcinolcarboxylic Acid (English)

18 November 2016

2 references

2,4-Dihydroxy-6-methylbenzoic acid (English)

18 November 2016

Reaxys registry number

2211027

1 reference

o-orsellinic acid (English)

19 October 2016

ChEBI ID

32807

mapping relation type

2 references

ORSELLINIC ACID (English)

18 November 2016

International Chemical Identifier

InChI

InChI=1S/C8H8O4/c1-4-2-5(9)3-6(10)7(4)8(11)12/h2-3,9-10H,1H3,(H,11,12)

1 reference

ORSELLINIC ACID (English)

18 November 2016

2 references

inferred from InChIKey

splash10-00di-0900000000-1875685211fff4102206

1 reference

0 references

DSSTox substance ID

DTXSID20197385

2 references

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

DSSTOX compound identifier

DTXCID30119876

0 references

EC number

610-404-4

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.115.964

27 December 2018

ECHA Substance Infocard ID

Benzoic acid, 2,4-dihydroxy-6-methyl- (English)

quotation

CAS no.: 480-64-8 (English)

100.115.964

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.115.964

27 December 2018

imported from Wikimedia project

Benzoic acid, 2,4-dihydroxy-6-methyl- (English)

quotation

CAS no.: 480-64-8 (English)

Nikkaji ID

J6.167K

1 reference

3 references

o-orsellinic acid (English)

19 October 2016

based on heuristic

inferred from InChIKey

UNII

11XLA0494B

2 references

Global Substance Registration System

UNII

11XLA0494B

orsellinic acid (English)

18 November 2016

Natural Product Atlas ID

NPA024876

2 references

based on heuristic

inferred from InChIKey

imported from Wikimedia project

0 references

1 reference

0 references

0 references

1 reference

28 October 2013

1 reference

9 July 2020

Microsoft Academic ID

0 references

1 reference

5KTH (English)