4',5,6,7-tetramethoxyflavone (Q27116014)

Scutellarein tetramethyl ether (English)

6 October 2016

chemical formula

C₁₉H₁₈O₆

1 reference

Scutellarein tetramethyl ether (English)

6 October 2016

canonical SMILES

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

1 reference

Exudate flavonoids from Ficus altissima

Scutellarein tetramethyl ether (English)

6 October 2016

2 references

Exudate flavonoids from Ficus altissima

Orthosiphon grandiflorus

5 references

Orthosiphol D and E, minor diterpenes from Orthosiphon stamineus

Five novel highly oxygenated diterpenes of Orthosiphon stamineus from Myanmar

Flavonoids from Orthosiphon spicatus

Constituents of the Vietnamese medicinal plant Orthosiphon stamineus.

Indonesian medicinal plants. XXIII. Chemical structures of two new migrated pimarane-type diterpenes, neoorthosiphols A and B, and suppressive effects on rat thoracic aorta of chemical constituents isolated from the leaves of Orthosiphon aristatus (

Marrubium velutinum

2 references

Identification of tyrosinase inhibitors from Marrubium velutinum and Marrubium cylleneum

Labdane diterpenes from Marrubium velutinum and Marrubium cylleneum

Cherry Orange

1 reference

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Marrubium peregrinum

1 reference

4′,5,6,7-Tetramethoxyflavone fromMarrubium peregrinum

Croton caudatus

1 reference

Flavonoids from the stems of Croton caudatus Geisel. var. tomentosus Hook.

Mentha aquatica var. citrata

1 reference

Free flavonoid aglycones from leaves of mentha pulegium and mentha suaveolens (labiatae)

Ageratina altissima

1 reference

Flavonoids from Eupatorium odoratum with Death Receptor 5 Promoter Enhancing Activity

Phellodendron amurense

1 reference

Rapid identification and comparative analysis of the chemical constituents and metabolites of Phellodendri amurensis cortex and Zhibai dihuang pill by ultra-performance liquid chromatography with quadrupole TOF-MS.

Kumquat

1 reference

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Citrus × deliciosa

5 references

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Discrimination of Citrus reticulata Blanco and Citrus reticulata 'Chachi' as well as the Citrus reticulata 'Chachi' within different storage years using ultra high performance liquid chromatography quadrupole/time-of-flight mass spectrometry based m

Studies on the differentiation inducers of myeloid leukemic cells from Citrus species.

Antioxidant Capacity, Anticancer Ability and Flavonoids Composition of 35 Citrus (Citrus reticulata Blanco) Varieties.

Tetramethyl-O-scutellarin isolated from peels of immature Shiranuhi fruit exhibits anti-inflammatory effects on LPSinduced RAW264.7 cells

Orthosiphon aristatus

5 references

Five novel highly oxygenated diterpenes of Orthosiphon stamineus from Myanmar

Flavonoids from Orthosiphon spicatus

Indonesian medicinal plants. XXIII. Chemical structures of two new migrated pimarane-type diterpenes, neoorthosiphols A and B, and suppressive effects on rat thoracic aorta of chemical constituents isolated from the leaves of Orthosiphon aristatus (

Constituents of the Vietnamese medicinal plant Orthosiphon stamineus.

Orthosiphol D and E, minor diterpenes from Orthosiphon stamineus

mandarin orange

5 references

Discrimination of Citrus reticulata Blanco and Citrus reticulata 'Chachi' as well as the Citrus reticulata 'Chachi' within different storage years using ultra high performance liquid chromatography quadrupole/time-of-flight mass spectrometry based m

Studies on the differentiation inducers of myeloid leukemic cells from Citrus species.

Antioxidant Capacity, Anticancer Ability and Flavonoids Composition of 35 Citrus (Citrus reticulata Blanco) Varieties.

Tetramethyl-O-scutellarin isolated from peels of immature Shiranuhi fruit exhibits anti-inflammatory effects on LPSinduced RAW264.7 cells

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Citrus japonica

1 reference

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Identifiers

InChI

InChI=1S/C19H18O6/c1-21-12-7-5-11(6-8-12)14-9-13(20)17-15(25-14)10-16(22-2)18(23-3)19(17)24-4/h5-10H,1-4H3

1 reference

Scutellarein tetramethyl ether (English)

6 October 2016

2 references

Scutellarein tetramethyl ether (English)

6 October 2016

ChEBI release 2020-09-01

2 references

4',5,6,7-tetramethoxyflavone (English)

6 October 2016

https://commonchemistry.cas.org/detail?cas_rn=1168-42-9

10 April 2021

1 reference

Tetramethyl-O-scutellarin (English)

6 October 2016

2 references

Scutellarein tetramethyl ether (English)

6 October 2016

Reaxys registry number

330766

1 reference

4',5,6,7-tetramethoxyflavone (English)

6 October 2016

ChEBI ID

34357

mapping relation type

2 references

4',5,6,7-tetramethoxyflavone (English)

6 October 2016

International Chemical Identifier

InChI

InChI=1S/C19H18O6/c1-21-12-7-5-11(6-8-12)14-9-13(20)17-15(25-14)10-16(22-2)18(23-3)19(17)24-4/h5-10H,1-4H3

1 reference

TETRAMETHYLSCUTELLAREIN (English)

6 October 2016

2 references

inferred from InChIKey

splash10-01ox-0369000000-38efb629b1fb86a82bb8

1 reference

0 references

DSSTox substance ID

DTXSID60151522

2 references

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

DSSTOX compound identifier

DTXCID4074013

0 references

NSC number

53908

0 references

Human Metabolome Database ID

HMDB0030575

2 references

based on heuristic

inferred from InChIKey

3 references

4',5,6,7-tetramethoxyflavone (English)

6 October 2016

based on heuristic

inferred from InChIKey

UNII

DWN851IYG6

1 reference

0 references

1 reference

4',5,6,7-tetramethoxyflavone (English)