rubiadin (Q15633911)

Rubiadin (English)

5 October 2016

C₁₅H₁₀O₄

1 reference

Rubiadin (English)

5 October 2016

CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O

1 reference

Identification of Alkaloids and Anthraquinones in Cinchona pubescens Callus Cultures; the Effect of Plant growth Regulators and Light on the Alkaloid Content

Rubiadin (English)

5 October 2016

1 reference

Prismatomeris fragrans

1 reference

Biological activity of Anthraquinones and Triterpenoids from Prismatomeris fragrans

Hedyotis capitellata

2 references

Anthraquinones from Hedyotis capitellata

Anthraquinones from Hedyotis capitellata

Cinchona calisaya

1 reference

Anthraquinones in callus cultures of Cinchona ledgeriana

Galium semiamictum

2 references

Anthraquinones of Galium semiamictum

Anthraquinones of Galium semiamictum

Galium spurium

2 references

Anthraquinones of Galium spurium

Anthraquinones of Galium spurium

Heterophyllaea pustulata

2 references

Pharmacological and toxicological activity of Heterophyllaea pustulata anthraquinone extracts

Antibacterial activity of anthraquinone derivatives from Heterophyllaea pustulata (Rubiaceae)

Hymenodictyon excelsum

2 references

Naturally occurring quinones. Part XIX. Anthraquinones in hymenodictyon excelsum and damnacanthus major

Naturally occurring quinones. Part XIX. Anthraquinones in hymenodictyon excelsum and damnacanthus major

Morinda elliptica

4 references

Anthraquinones in cell suspension cultures of Morinda citrifolia

Anthraquinones from Morinda elliptica

Antiviral, cyototoxic and antimicrobial activities of anthraquinones isolated from the roots of morinda elliptica.

Anthraquinones from Morinda elliptica

Prismatomeris sessiliflora

2 references

Antimalarials from Stephania venosa, Prismatomeris sessiliflora, Diospyros montana and Murraya siamensis

Antimalarials from Stephania venosa, Prismatomeris sessiliflora, Diospyros montana and Murraya siamensis

Sweet Woodruff

1 reference

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

Coelospermum paniculatum

1 reference

Colouring Matters of Australian Plants. X. Anthraquinones from Coelospermum Species

Coprosma lucida

2 references

611. Chemistry of the Coprosma genus. Part VII. A revised constitution for lucidin

269. Chemistry of the coprosma genus. Part IV. The non-glycosidic anthraquinone compounds from coprosma lucida

Faramea occidentalis

1 reference

Two naphthopyran derivatives from Faramea cyanea

Oldenlandia hedyotidea

1 reference

New Anthraquinone and Iridoid Glycosides from the Stems of Hedyotis hedyotidea

Morinda angustifolia

1 reference

Antimicrobial anthraquinones from Morinda angustifolia.

Gynochthodes jasminoides

1 reference

Colouring Matters of Australian Plants. IX. Anthraquinones from Morinda Species

Ophiorrhiza hayatana

1 reference

Anthraquinones from Ophiorrhiza hayatana OHWI

Plocama pendula

1 reference

Anthraquinones from natural and transformed roots of Plocama pendula

Rennellia elliptica

1 reference

Anthraquinones with antiplasmodial activity from the roots of Rennellia elliptica Korth. (Rubiaceae).

Rubia alata

1 reference

Constituents of Roots of Rubia Lanceolata Hayata

Rubia lanceolata

1 reference

Constituents of Roots of Rubia Lanceolata Hayata

Coprosma tenuicaulis

1 reference

Chemistry of the Coprosma genus. Part XIV. Constituents of five New Zealand species

Coprosma rotundifolia

1 reference

Chemistry of the Coprosma genus. Part XIV. Constituents of five New Zealand species

Coprosma linariifolia

1 reference

Chemistry of the Coprosma genus. Part XIV. Constituents of five New Zealand species

Coprosma robusta

1 reference

Chemistry of the Coprosma genus. Part XIV. Constituents of five New Zealand species

Prismatomeris tetrandra

2 references

Anthraquinones from the roots of Prismatomeris tetrandra

Anthraquinones from the Roots of Prismatomeris tetrandra.

Rubia cordifolia

3 references

Anthraquinones and naphthohydroquinones from Rubia cordifolia

New Anthraquinones from Rubia cordifolia Roots

Hepatoprotective effects of rubiadin, a major constituent of Rubia cordifolia Linn

Rubia tinctorum

3 references

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

The mutagenic constituents of Rubia tinctorum

2 references

Cytotoxic anthraquinones from the stems of Rubia wallichiana Decne

Cytotoxic Anthraquinones from the Stems of Rubia wallichiana Decne

Rubia yunnanensis

2 references

Biologically active arborinane-type triterpenoids and anthraquinones from Rubia yunnanensis

Constituents of the roots of Rubia yunnanensis

Galium dasypodum

1 reference

Anthraquinones ofGalium dasypodum

Senna multijuga

1 reference

Anthraquinones and Anthraquinone Glycosides from the Roots of Cassia multijuga

Ophiorrhiza pumila

1 reference

Anthraquinones from Ophiorrhiza pumila tissue and cell cultures

Galium verum

1 reference

Novel anthraquinones from undifferentiated cell cultures of galium verum

Morinda citrifolia

7 references

Anthraquinones in cell suspension cultures of Morinda citrifolia

Anthraquinones from Morinda elliptica

Antiviral, cyototoxic and antimicrobial activities of anthraquinones isolated from the roots of morinda elliptica.

Anthraquinones with quinone reductase-inducing activity and benzophenones from Morinda citrifolia (noni) roots.

Anthraquinone Content in Noni (Morinda citrifolia L.)

Chemical components of the roots of Noni (Morinda citrifolia) and their cytotoxic effects

Isolation, identification and biosynthesis of anthraquinones in cell suspension cultures of Morinda citrifolia (author's transl)

Hymenodictyon orixense

1 reference

Naturally occurring quinones. Part XIX. Anthraquinones in hymenodictyon excelsum and damnacanthus major

Galium aparine

1 reference

Anthraquinones of Galium spurium

Gynochthodes officinalis

2 references

Some Chemical Constituents of Morinda citrifolia

Chemical constituents of Chinese natural medicine, morindae radix, the dried roots of morinda officinalis how.: structures of morindolide and morofficinaloside

Galium rubioides

2 references

Anthraquinones ofGalium dasypodum

Anthraquinones of Gallium articulatum

Identifiers

InChI

InChI=1S/C15H10O4/c1-7-11(16)6-10-12(13(7)17)15(19)9-5-3-2-4-8(9)14(10)18/h2-6,16-17H,1H3

1 reference

IRZTUXPRIUZXMP-UHFFFAOYSA-N

Rubiadin (English)

5 October 2016

2 references

Rubiadin (English)

5 October 2016

ChEBI release 2020-09-01

2 references

IRZTUXPRIUZXMP-UHFFFAOYSA-N

rubiadin (English)

5 October 2016

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=117-02-2

1 reference

Rubiadin (English)

5 October 2016

1 reference

English

title

Rubiadin (English)

5 October 2016

Reaxys registry number

1885558

1 reference

rubiadin (English)

5 October 2016

mapping relation type

1 reference

rubiadin (English)

5 October 2016

1 reference

splash10-0a4i-0490000000-65dc3831c89d40a24918

Rubiadin (English)

5 October 2016

1 reference

0 references

DSSTox substance ID

DTXSID90151651

1 reference

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

DSSTOX compound identifier

DTXCID4074142

0 references

EC number

683-093-6

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.613

ECHA Substance Infocard ID

27 December 2018

title

[No public or meaningful name is available] (English)

quotation

CAS no.: 117-02-2 (English)

100.208.613

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.613

Human Metabolome Database ID

27 December 2018

title

[No public or meaningful name is available] (English)

quotation

CAS no.: 117-02-2 (English)

HMDB0257354

1 reference

based on heuristic

inferred from InChIKey

2 references

rubiadin (English)

5 October 2016

inferred from InChIKey

UNII

CY0UH3X06R

1 reference

Global Substance Registration System

UNII

CY0UH3X06R

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

RUBIADIN (English)

5 October 2016

0 references

1 reference