(Q27258607)

Chloroatranorin (English)

14 October 2016

chemical formula

C₁₉H₁₇ClO₈

1 reference

Chloroatranorin (English)

14 October 2016

canonical SMILES

CC1=CC(=C(C(=C1C(=O)OC)O)C)OC(=O)C2=C(C(=C(C(=C2O)C=O)O)Cl)C

1 reference

The occurrence of lichen phenolics in the xylem sap of Quercus pyrenaica, their translocation to leaves and biological significance

Chloroatranorin (English)

14 October 2016

3 references

Preparation of an oakmoss absolute with reduced allergenic potential

The lichen substances of the genus Evernia

Lecanora planaica

1 reference

New Depsides From the Lichen Lecanora planaica

Parmotrema demethylmicrophyllinicum

1 reference

The Isolation and Synthesis of the Lichen Depside 4-O-Demethylmicrophyllinic Acid

Menegazzia asahinae

1 reference

On the constituents of the lichen in the genus Menegazzia. Menegazziaic acid, a new depsidone from Menegazzia asahinae (Yas. ex Zahlbr.) Sant. and Menegazzia terebrata (Hoffm.) Mass.

Menegazzia terebrata

1 reference

On the constituents of the lichen in the genus Menegazzia. Menegazziaic acid, a new depsidone from Menegazzia asahinae (Yas. ex Zahlbr.) Sant. and Menegazzia terebrata (Hoffm.) Mass.

Hypotrachyna horrescens

1 reference

4,5-Di-O-methylhiascic acid, a new tridepside from the lichens Parmelia pseudofatiscens and Parmelia horrescens

Parmelia

1 reference

4,5-Di-O-methylhiascic acid, a new tridepside from the lichens Parmelia pseudofatiscens and Parmelia horrescens

Anzia hypoleucoides

1 reference

Sublobaric Acid and Oxolobaric Acid, Two New Depsidones from the Lichen Anzia hypoleucoides

Hypotrachyna leiophylla

1 reference

A New Chloro-Depside from the Lichen Hypotrachyna leiophylla

Hypotrachyna quaesita

1 reference

The Structure of Chalybaeizanic Acid and Quaesitic Acid, Two New Lichen Depsidones Related to Salazinic Acid

Lecanora argentata

1 reference

Further New Metabolites From Lichens

Lecanora californica

1 reference

Further New Metabolites From Lichens

Lecanora elixii

1 reference

The Joint Occurrence of Chloroxanthones in Southern HemisphereLecanoraSpecies (Ascomycotina; Lecanoraceae)

Lecanora lividocinerea

1 reference

New Chloro Depsides from the Lichen Lecanora lividocinerea

Lecanora mayrhoferi

1 reference

The Joint Occurrence of Chloroxanthones in Southern HemisphereLecanoraSpecies (Ascomycotina; Lecanoraceae)

Lecanora myriocarpoides

1 reference

Conhypoprotocetraric Acid, a New Lichen β-Orcinol Depsidone

Lotus uliginosus

1 reference

Proanthocyanidins from Lotus pedunculatus

Menegazzia dispora

1 reference

α-Acetylhypoconstictic Acid, a New Depsidone from the Lichen Menegazzia dispora

Hypotrachyna nepalensis

1 reference

Isolation and identification of some chemical constituents of Parmelia nepalensis

Notoparmelia norcrambidiocarpa

1 reference

The Structure of Echinocarpic Acid. A Benzyl Ester From the Lichen Parmelia norcrambidiocarpa

Parmelia tinctoria

1 reference

Chemical constituents from Paris mairei

Parmotrema nilgherrense

1 reference

Dehydrocollatolic Acid, a New Depsidone from the Lichen Parmotrema nilgherrense

Parmotrema praesorediosum

1 reference

Two New Aliphatic Acids From the Lichen Parmotrema praesorediosum

Platismatia glauca

1 reference

Isolation of 30-nor-21 α-hopan-22-one (isoadiantone) from the lichen Platismatia glauca

Tylothallia pahiensis

1 reference

Further New Metabolites From Lichens

Candelaria concolor

1 reference

Chemical constituents of the lichen, Candelaria concolor: a complete NMR and chemical degradative investigation.

Lecanora gangaleoides

1 reference

Phytochemical examination of the lichen, Lecanora gangaleoides Nyl

Hypotrachyna neodamaziana

2 references

2,4-Di-O-methylgyrophoric acid and 2,4,5-tri-O-methylhiascic acid. New tridepsides from Parmelia damaziana

2-O-Methylhiascic Acid, a New Tridepside in the Lichen Parmelinopsis neodamaziana

Lotus pedunculatus

1 reference

Proanthocyanidins from Lotus pedunculatus

Parmotrema tinctorum

2 references

Chemical constituents from Paris mairei

Antimicrobial activity of compounds isolated from algae

Physcia mediterranea

1 reference

Phytochemical Investigation of New Algerian Lichen Species: Physcia Mediterranea Nimis

Hypogymnia tubulosa

1 reference

Hypogymnia tubulosa extracts: chemical profile and biological activities.

subject has role

antimicrobial agent

1 reference

Antimicrobial activity of extracts of chemical races of the lichen Pseudevernia furfuracea and their physodic acid, chloroatranorin, atranorin, and olivetoric acid constituents.

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

Identifiers

InChI

InChI=1S/C19H17ClO8/c1-7-5-11(8(2)15(22)12(7)18(25)27-4)28-19(26)13-9(3)14(20)17(24)10(6-21)16(13)23/h5-6,22-24H,1-4H3

1 reference

Chloroatranorin (English)

14 October 2016

2 references

Chloroatranorin (English)

14 October 2016

ChEBI release 2020-09-01

CAS Registry Number

479-16-3

1 reference

Global Substance Registration System

UNII

433PEB1G7C

chloroatranorin (English)

14 October 2016

1 reference

3-Hydroxy-4-(methoxycarbonyl)-2,5-dimethylphenyl 3-chloro-5-formyl-4,6-dihydroxy-2-methylbenzoate (English)

14 October 2016

2 references

Chloroatranorin (English)

14 October 2016

ChEBI ID

144138

mapping relation type

exact match

2 references

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C19H17ClO8/c1-7-5-11(8(2)15(22)12(7)18(25)27-4)28-19(26)13-9(3)14(20)17(24)10(6-21)16(13)23/h5-6,22-24H,1-4H3

1 reference

2 references

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

DSSTOX compound identifier

0 references

2 references

inferred from InChIKey

UNII

433PEB1G7C

2 references

Global Substance Registration System

UNII

433PEB1G7C

chloroatranorin (English)

14 October 2016