(Q116472)

imported from Wikimedia project

Medical Subject Headings

15 March 2018

1,2,4-trihydroxyanthracene-9,10-dione 200.svg
200 × 134; 7 KB

1 reference

German Wikipedia

image

Purpurin powder crop.jpg
678 × 1,278; 323 KB

0 references

mass

256.037 dalton

1 reference

PURPURIN (English)

5 October 2016

C₁₄H₈O₅

1 reference

PURPURIN (English)

5 October 2016

C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3O)O)O

1 reference

Anthraquinones as phytoalexins in cell and tissue cultures of Cinchona spec.

PURPURIN (English)

5 October 2016

2 references

Anthraquinones in callus cultures of Cinchona pubescens

Cinchona calisaya

4 references

Anthraquinones as phytoalexins in cell and tissue cultures of Cinchona spec.

Anthraquinones in callus cultures of Cinchona ledgeriana

The production of anthraquinones by cell suspension cultures of Cinchona ledgeriana

Anthraquinones in callus cultures of Cinchona ledgeriana

Rubia wallichiana

2 references

Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne

Cytotoxic Anthraquinones from the Stems of Rubia wallichiana Decne

Senna obtusifolia

1 reference

Emodin isolated from Cassia obtusifolia (Leguminosae) seed shows larvicidal activity against three mosquito species

Rubia tinctorum

7 references

Anthraquinone production by transformed root cultures of Rubia tinctorum: Influence of phytohormones and sucrose concentration

High-performance liquid chromatographic method for the analysis of anthraquinone glycosides and aglycones in madder root (Rubia tinctorum L.)

Naturally occurring quinones. Part XV. Biogenesis of the anthraquinones in Rubia tinctorum L. (madder)

HPLC Analysis of Anthraquinone Derivatives in Madder Root (Rubia Tinctorum) and Its Cell Cultures

Rubia tinctorum L.

Naturally occurring quinones. Part XV. Biogenesis of the anthraquinones in Rubia tinctorum L. (madder)

Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne

Tephrosia purpurea

1 reference

Flavonoids of Tephrosia polyphylla

Agrobacterium rhizogenes

2 references

A piperidone alkaloid from Hyoscyamus albus roots transformed with Agrobacterium rhizogenes

Alkaloid production in hairy roots of Hyoscyamus albus transformed with Agrobacterium rhizogenes

Sweet Woodruff

1 reference

Naturally occurring quinones. Part XIII. Anthraquinones and related naphthalenic compounds in Galium spp. and in Asperula odorata

Rubia cordifolia

2 references

The Pigments in the Root of Japanese " Akane " (Rubia cordifolia var munjista. Miq. )

Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne

Rubia manjith

1 reference

The Pigments in the Root of Japanese " Akane " (Rubia cordifolia var munjista. Miq. )

Rubia akane

1 reference

Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne

Galium mollugo

1 reference

Biosynthesis of anthraquinones and related compounds in Galium mollugo cell suspension cultures

Rhizobium rhizogenes

2 references

A piperidone alkaloid from Hyoscyamus albus roots transformed with Agrobacterium rhizogenes

Alkaloid production in hairy roots of Hyoscyamus albus transformed with Agrobacterium rhizogenes

Rubia argyi

1 reference

Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne

Galium rubioides

1 reference

Anthraquinones of Gallium articulatum

described by source

Meyers Konversations-Lexikon, 4th edition (1885–1890)

statement is subject of

Q112792568

0 references

Commons category

Purpurin

0 references

Identifiers

InChI

InChI=1S/C14H8O5/c15-8-5-9(16)14(19)11-10(8)12(17)6-3-1-2-4-7(6)13(11)18/h1-5,15-16,19H

1 reference

BBNQQADTFFCFGB-UHFFFAOYSA-N

PURPURIN (English)

5 October 2016

2 references

PURPURIN (English)

5 October 2016

ChEBI release 2020-09-01

2 references

BBNQQADTFFCFGB-UHFFFAOYSA-N

purpurin (English)

5 October 2016

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=81-54-9

1 reference

English

1,2,4-Trihydroxyanthraquinone (English)

5 October 2016

1 reference

English

PURPURIN (English)

5 October 2016

Reaxys registry number

1887127

1 reference

purpurin (English)

5 October 2016

271628

0 references

ChEBI ID

8645

mapping relation type

1 reference

purpurin (English)

5 October 2016

1 reference

splash10-0a4i-0090000000-fdf6f240d32f873d58bb

PURPURIN (English)

5 October 2016

1 reference

MassBank accession ID

SM837253

0 references

SPLASH

0 references

DSSTox substance ID

DTXSID4021214

1 reference

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

DSSTOX compound identifier

0 references

0 references

201-359-8

1 reference

Global Substance Registration System

UNII

L1GT81LS6N

English

PURPURIN (English)

ECHA Substance Infocard ID

5 October 2016

100.001.237

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.001.237

27 December 2018

1,2,4-trihydroxyanthraquinone (English)

quotation

CAS no.: 81-54-9 (English)

MeSH descriptor ID

C511975

1 reference

Medical Subject Headings

MeSH descriptor ID

C511975

Human Metabolome Database ID

14 March 2018

HMDB0256928

1 reference

based on heuristic

inferred from InChIKey

2 references

purpurin (English)

5 October 2016

inferred from InChIKey

UNII

L1GT81LS6N

1 reference

Global Substance Registration System

UNII

L1GT81LS6N

PURPURIN (English)

5 October 2016

0 references

1 reference

Immune Epitope Database and Analysis Resource

purpurin (English)

5 October 2016

1 reference

1 March 2022

0 references

1 reference

28 October 2013

Gran Enciclopèdia Catalana ID

purpurina

0 references

Gran Enciclopèdia Catalana ID (former scheme)

0204713

0 references

Microsoft Academic ID

0 references

1 reference

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023