(Q7103718)

Orobol (English)

5 October 2016

C₁₅H₁₀O₆

1 reference

Orobol (English)

5 October 2016

C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O

1 reference

Orobol (English)

5 October 2016

Bolusanthus speciosus

3 references

Alkaloids of Bolusanthus speciosus

Isoflavonoids from Bolusanthus speciosus (Bolus) Harms Leguminosae

Seed flavonoids of thePodalyrieae andLiparieae (Fabaceae)

Maclura tinctoria

3 references

Anaxagorea luzonensis

1 reference

Studies on the constituents of Anaxagorea luzonensis A. GRAY.

Aster heliopsis

1 reference

Studies on the constituents of the leaves of Acer negundo (L.)

Cladrastis platycarpa

1 reference

A New Pterocarpan from the Heartwood of Cladrastis platycarpa

Glycyrrhiza uralensis

1 reference

Minor flavonoids from licorice

Mucuna membranacea

2 references

Chemical Constituents from Mucuna membranacea

Chemical Constituents from Mucuna membranacea

Styphnolobium japonicum

2 references

Sophoricoside analogs as the IL-5 inhibitors from Sophora japonica

Sophoricoside analogs as the IL-5 inhibitors from Sophora japonica

Soroseris hookeriana

2 references

New antimicrobial mono- and sesquiterpenes from Soroseris hookeriana subsp. erysimoides

New antimicrobial mono- and sesquiterpenes from Soroseris hookeriana subsp. erysimoides

Thermopsis dolichocarpa

2 references

Flavonoids of Thermopsis dolichocarpa

Flavonoids of Thermopsis dolichocarpa

Trifolium pratense

1 reference

Identification of isoflavone conjugates in red clover (Trifolium pratense) by liquid chromatography–mass spectrometry after two-dimensional solid-phase extraction

Tritirachium

1 reference

Inhibition of 15-lipoxygenase by orobol

Wyethia angustifolia

2 references

Flavonoids of Wyethia angustifolia and W. helenioides

Flavonoids of Wyethia angustifolia and W. helenioides

Ophiocordyceps sinensis

2 references

Anti-inflammatory principles from Cordyceps sinensis

Anti-inflammatory principles from Cordyceps sinensis

Dalbergia odorifera

1 reference

Inhibitory constituents of the heartwood of Dalbergia odorifera on nitric oxide production in RAW 264.7 macrophages

Streptomyces avermitilis

2 references

Isolation of isoflavones inhibiting dopa decarboxylase from fungi and streptomyces.

Regioselective hydroxylation of isoflavones by Streptomyces avermitilis MA-4680.

Ammopiptanthus mongolicus

1 reference

Three New Isoflavonoids from the Aerial Parts ofAmmopiptanthus mongolicus

Calophyllum polyanthum

1 reference

Two pyranocoumarins from the seeds of Calophyllum polyanthum

Cyclopia subternata

1 reference

Phenolic metabolites from honeybush tea (Cyclopia subternata).

Dalbergia parviflora

1 reference

Cytotoxicity of chemical constituents from the stems of Dalbergia parviflora

Desmodium styracifolium

1 reference

Isoflavanones and their O-glycosides from Desmodium styracifolium

Maackia amurensis

1 reference

Polyphenols from Maackia amurensis Root Bark

Dalbergia paniculata

1 reference

Isoflavonoid glycosides of Dalbergia paniculata

Baptisia

1 reference

Distribution of flavonoids in the genus baptisia (leguminosae)

Flemingia macrophylla

2 references

Neuroprotective flavonoids from Flemingia macrophylla

Prenylated flavonoids from Moghania philippinensis

Maclura tricuspidata

4 references

Flavonoids, including an unusual flavonoid-Mg2+ salt, from roots of Cudrania cochinchinensis

Flavonoids and a prenylated xanthone from Cudrania cochinchinensis var. gerontogea

Prenylated and benzylated flavonoids from the fruits of Cudrania tricuspidata

Maclura cochinchinensis

3 references

Flavonoids and a prenylated xanthone from Cudrania cochinchinensis var. gerontogea

Flavonoids, including an unusual flavonoid-Mg2+ salt, from roots of Cudrania cochinchinensis

Dermatophyllum secundiflorum

1 reference

Isoflavonoids from Sophora secundiflora, S. arizonica and S. gypsophila

Flemingia prostrata

1 reference

Prenylated flavonoids from Moghania philippinensis

Streptomyces

1 reference

Isolation and Structure Determination of Novel Phosphatidylinositol Kinase Inhibitors, Echiguanines A and B, from Streptomyces sp

Commons category

Orobol

0 references

Identifiers

InChI

InChI=1S/C15H10O6/c16-8-4-12(19)14-13(5-8)21-6-9(15(14)20)7-1-2-10(17)11(18)3-7/h1-6,16-19H

1 reference

Orobol (English)

5 October 2016

2 references

Orobol (English)

5 October 2016

ChEBI release 2020-09-01

2 references

orobol (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=480-23-9

9 April 2021

1 reference

Orobol (English)

5 October 2016

2 references

English

title

Orobol (English)

retrieved

5 October 2016

Reaxys registry number

292790

1 reference

orobol (English)

5 October 2016

mapping relation type

2 references

English

title

orobol (English)

retrieved

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C15H10O6/c16-8-4-12(19)14-13(5-8)21-6-9(15(14)20)7-1-2-10(17)11(18)3-7/h1-6,16-19H

1 reference

OROBOL (English)

5 October 2016

2 references

inferred from InChIKey

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

1 reference

2 references

DSSTOX compound identifier

DTXCID30119871

0 references

Human Metabolome Database ID

HMDB0041658

2 references

based on heuristic

inferred from InChIKey

3 references

orobol (English)

5 October 2016

inferred from InChIKey

UNII

LU8UZM1T51

2 references

Global Substance Registration System

UNII

LU8UZM1T51

English

title

OROBOL (English)

retrieved

5 October 2016