apigenin trimethyl ether (Q27277645)

4',5,7-Trimethoxyflavone (English)

14 October 2016

chemical formula

C₁₈H₁₆O₅

1 reference

4',5,7-Trimethoxyflavone (English)

14 October 2016

canonical SMILES

COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)OC

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

4',5,7-Trimethoxyflavone (English)

14 October 2016

1 reference

Citrus intermedia

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus otachibana

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus myrtifolia

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus nippokoreana

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus unshiu

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus tachibana

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Cherry Orange

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Tanacetum vulgare

1 reference

Germacranolides and an alkyl glucoside from Tanacetum vulgare

Gonocaryum calleryanum

1 reference

Secoiridoid and flavonoid glycosides from Gonocaryum calleryanum

Kaempferia parviflora

5 references

Bioactive flavonoids from Kaempferia parviflora

Phenolic glycosides from Kaempferia parviflora

Structures of two new phenolic glycosides, kaempferiaosides A and B, and hepatoprotective constituents from the rhizomes of Kaempferia parviflora

Cytotoxicity against KB and NCI-H187 cell lines of modified flavonoids from Kaempferia parviflora

Modulation of function of multidrug resistance associated-proteins by Kaempferia parviflora extracts and their components

Orthosiphon grandiflorus

1 reference

Flavonoids from Orthosiphon spicatus

Streptomyces avermitilis

1 reference

High-yield production of multiple O-methylated phenylpropanoids by the engineered Escherichia coli-Streptomyces cocultivation system

Boesenbergia rotunda

2 references

Flavonoids in the black rhizomes of Boesenbergia panduta

Anti-inflammatory cyclohexenyl chalcone derivatives in Boesenbergia pandurata

Citrus hassaku

1 reference

On the flavonoid constituents from the peels of Citrus hassaku Hort. ex. Tanaka.

Piper cubeba

1 reference

Radical scavenging ability of some compounds isolated from Piper cubeba towards free radicals

Piper porphyrophyllum

1 reference

Chemical constituents from tiger's betel, Piper porphyrophyllum N.E.Br. (Fam. Piperaceae).

Bryobium erioides

4 references

Structures of two new phenolic glycosides, kaempferiaosides A and B, and hepatoprotective constituents from the rhizomes of Kaempferia parviflora

Phenolic glycosides from Kaempferia parviflora

Modulation of function of multidrug resistance associated-proteins by Kaempferia parviflora extracts and their components

Cytotoxicity against KB and NCI-H187 cell lines of modified flavonoids from Kaempferia parviflora

Citrus × paradisi

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Bryobium eriaeoides

4 references

Phenolic glycosides from Kaempferia parviflora

Structures of two new phenolic glycosides, kaempferiaosides A and B, and hepatoprotective constituents from the rhizomes of Kaempferia parviflora

Modulation of function of multidrug resistance associated-proteins by Kaempferia parviflora extracts and their components

Cytotoxicity against KB and NCI-H187 cell lines of modified flavonoids from Kaempferia parviflora

Zingiber officinale

1 reference

Characterization of phenolic compounds from normal ginger (Zingiber officinale Rosc.) and black ginger (Kaempferia parviflora Wall.) using UPLC–DAD–QToF–MS

mandarin orange

2 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Studies on the constituents of useful plants. V. Multisubstituted flavones in the fruit peel of Citrus reticulata and their examination by gas-liquid chromatography.

Citrus × deliciosa

2 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Studies on the constituents of useful plants. V. Multisubstituted flavones in the fruit peel of Citrus reticulata and their examination by gas-liquid chromatography.

Kumquat

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

pomelo

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus medica

2 references

On the flavonoid constituents from the peels of Citrus hassaku Hort. ex. Tanaka.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Orthosiphon aristatus

1 reference

Flavonoids from Orthosiphon spicatus

Citrus japonica

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

1 reference

Identifiers

InChI

InChI=1S/C18H16O5/c1-20-12-6-4-11(5-7-12)15-10-14(19)18-16(22-3)8-13(21-2)9-17(18)23-15/h4-10H,1-3H3

1 reference

4',5,7-Trimethoxyflavone (English)

14 October 2016

1 reference

Global Substance Registration System

4',5,7-Trimethoxyflavone (English)

14 October 2016

2 references

UNII

F50JU8E74U

apigenin trimethyl ether (English)

14 October 2016

https://commonchemistry.cas.org/detail?cas_rn=5631-70-9

9 April 2021

1 reference

Apigenin trimethyl ether (English)

14 October 2016

2 references

4',5,7-Trimethoxyflavone (English)

14 October 2016

ChEBI ID

174981

mapping relation type

exact match

2 references

ChEBI release 2022-06-13

International Chemical Identifier

InChI

InChI=1S/C18H16O5/c1-20-12-6-4-11(5-7-12)15-10-14(19)18-16(22-3)8-13(21-2)9-17(18)23-15/h4-10H,1-3H3

1 reference

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

TRIMETHYLAPIGENIN (English)

14 October 2016

1 reference

2 references

DSSTOX compound identifier

DTXCID40127346

0 references

Human Metabolome Database ID

HMDB0030842

2 references

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00003821

2 references

based on heuristic

inferred from InChIKey

UNII

F50JU8E74U

2 references

Global Substance Registration System

UNII

F50JU8E74U

apigenin trimethyl ether (English)

14 October 2016

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

0 references

1 reference