lichexanthone

Lichexanthone (English)

7 October 2016

chemical formula

C₁₆H₁₄O₅

1 reference

Lichexanthone (English)

7 October 2016

canonical SMILES

CC1=CC(=CC2=C1C(=O)C3=C(C=C(C=C3O2)OC)O)OC

1 reference

Effect of lichen metabolites on thylakoid electron transport and photophosphorylation in isolated spinach chloroplasts

Lichexanthone (English)

7 October 2016

1 reference

Aspidosperma formosanum

1 reference

Alkaloids of three Aspidosperma species

Croton cuneatus

1 reference

Three new glutarimide alkaloids from Croton cuneatus

Pyxine berteriana

1 reference

Fernene triterpenoids from the lichen Pyxine berteriana

Minquartia guianensis

1 reference

Triterpenes, lichexanthone and an acetylenic acid from Minquartia guianensis

Rauvolfia mattfeldiana

1 reference

A New Depside Isolated from the Bark of Rauwolfia mattfeldiana

Zanthoxylum tetraspermum

1 reference

Antimicrobial alkaloids from Zanthoxylum tetraspermum and caudatum

Henriettea fascicularis

1 reference

Isolation and structure elucidation of an isoflavone and a sesterterpenoic acid from Henriettella fascicularis

Ruprechtia tangarana

1 reference

Isolation and structure of ruprechstyril from Ruprechtia tangarana

Gustavia hexapetala

2 references

Isolation and structure of gustastatin from the Brazilian nut tree Gustavia hexapetala

Isolation and Structure of Gustastatin from the Brazilian Nut Tree Gustavia hexapetala, 1

Polyscias fulva

1 reference

Constituents isolated from Polyscias fulva

Inga punctata

1 reference

Plant Anticancer Agents. IX. Constituents of Hyptis tomentosa

Nectandra turbacensis

1 reference

Lignans from Nectandra turbacensis

Anthocleista djalonensis

1 reference

A new phthalide and xanthones from Anthocleista djalonensis and Anthocleista vogelli

Dialium excelsum

1 reference

Dialiumoside, an Olean-18-ene Triterpenoid from Dialium excelsum

Faramea occidentalis

1 reference

Two naphthopyran derivatives from Faramea cyanea

Guatteria blepharophylla

1 reference

Chemical constituents isolated from the bark of Guatteria blepharophylla (Annonaceae) and their antiproliferative and antimicrobial activities

Vepris glaberrima

1 reference

Alkaloids from Oriciopsis glaberrima Engl. (Rutaceae)

Parmotrema reticulatum

1 reference

Isolation, characterization and antifungal activity of major constituents of the Himalayan lichen Parmelia reticulata Tayl

Zanthoxylum rhoifolium

1 reference

A chromone from Zanthoxylum species

Wikstroemia lanceolata

1 reference

New lignans and cytotoxic constituents from Wikstroemia lanceolata

Talaromyces diversus

1 reference

The structures of some metabolites of Penicillium diversum: α-and β-diversonolic esters

Penicillium diversum

1 reference

The structures of some metabolites of Penicillium diversum: α-and β-diversonolic esters

Parmotrema lichexanthonicum

2 references

Cytotoxic evaluation of phenolic compounds from lichens against melanoma cells

Antimycobacterial activity of lichen substances

Cupania cinerea

1 reference

Antiparasitic compounds from Cupania cinerea with activities against Plasmodium falciparum and Trypanosoma brucei rhodesiense

subject has role

antineoplastic

1 reference

Cytotoxic evaluation of phenolic compounds from lichens against melanoma cells

antimicrobial agent

1 reference

Antimycobacterial activity of lichen substances

Commons category

Lichexanthone

0 references

Identifiers

InChI

InChI=1S/C16H14O5/c1-8-4-9(19-2)6-12-14(8)16(18)15-11(17)5-10(20-3)7-13(15)21-12/h4-7,17H,1-3H3

1 reference

Lichexanthone (English)

7 October 2016

2 references

Lichexanthone (English)

7 October 2016

ChEBI release 2020-09-01

2 references

lichexanthone (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=15222-53-4

10 April 2021

1 reference

Xanthen-9-one, 1-hydroxy-3,6-dimethoxy-8-methyl- (English)

7 October 2016

2 references

Lichexanthone (English)

7 October 2016

Reaxys registry number

274869

1 reference

lichexanthone (English)

7 October 2016

ChEBI ID

67821

mapping relation type

2 references

lichexanthone (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C16H14O5/c1-8-4-9(19-2)6-12-14(8)16(18)15-11(17)5-10(20-3)7-13(15)21-12/h4-7,17H,1-3H3

1 reference

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

LICHEXANTHONE (English)

7 October 2016

1 reference

2 references

DSSTOX compound identifier

0 references

0 references

3 references

lichexanthone (English)

7 October 2016

based on heuristic

inferred from InChIKey

UNII

92O5D9Z07W

1 reference