Chemical Formula: C18H16O5
Chemical Formula C18H16O5
Found 179 metabolite its formula value is C18H16O5
5,6,7-Trimethoxyflavone
5,6,7-Trimethoxyflavone is a novel p38-α MAPK inhibitor with an anti-inflammatory effect. 5,6,7-Trimethoxyflavone is isolated from several plants including Zeyhera tuberculosa, Callicarpa japonica, and Kickxia lanigera[1]. 5,6,7-Trimethoxyflavone is a novel p38-α MAPK inhibitor with an anti-inflammatory effect. 5,6,7-Trimethoxyflavone is isolated from several plants including Zeyhera tuberculosa, Callicarpa japonica, and Kickxia lanigera[1].
4',5,7-Trimethoxyflavone
4,5,7-Trimethoxyflavone, also known as trimethylapigenin, belongs to the class of organic compounds known as 7-O-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Thus, 4,5,7-trimethoxyflavone is considered to be a flavonoid lipid molecule. 4,5,7-Trimethoxyflavone is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, 4,5,7-trimethoxyflavone has been detected, but not quantified in, a few different foods, such as citrus, mandarin orange (clementine, tangerine), and sweet oranges. This could make 4,5,7-trimethoxyflavone a potential biomarker for the consumption of these foods. 4,5,7-Trimethoxyflavone is an ether and a member of flavonoids. 4,5,7-Trimethoxyflavone is a natural product found in Tanacetum vulgare, Citrus medica, and other organisms with data available. See also: Tangerine peel (part of). Occurs in the peel of Citrus reticulata (mandarin). 4,5,7-Trimethylapigenin is found in sweet orange and citrus. 5,7,4'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) that is a famous medicinal plant from Thailand. 5,7,4'-Trimethoxyflavone induces apoptosis, as evidenced by increments of sub-G1 phase, DNA fragmentation, annexin-V/PI staining, the Bax/Bcl-xL ratio, proteolytic activation of caspase-3, and degradation of poly (ADP-ribose) polymerase (PARP) protein.5,7,4'-Trimethoxyflavone is significantly effective at inhibiting proliferation of SNU-16 human gastric cancer cells in a concentration dependent manner[1]. 5,7,4'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) that is a famous medicinal plant from Thailand. 5,7,4'-Trimethoxyflavone induces apoptosis, as evidenced by increments of sub-G1 phase, DNA fragmentation, annexin-V/PI staining, the Bax/Bcl-xL ratio, proteolytic activation of caspase-3, and degradation of poly (ADP-ribose) polymerase (PARP) protein.5,7,4'-Trimethoxyflavone is significantly effective at inhibiting proliferation of SNU-16 human gastric cancer cells in a concentration dependent manner[1].
2',5,6-Trimethoxyflavone
2,5,6-Trimethoxyflavone is found in pomes. 2,5,6-Trimethoxyflavone is isolated from Casimiroa edulis (Mexican apple). Isolated from Casimiroa edulis (Mexican apple). 2,5,6-Trimethoxyflavone is found in pomes.
2-(2H-1,3-benzodioxol-5-yl)-5-(3-hydroxypropyl)-1-benzofuran-7-ol
5-Hydroxy-4',7-dimethoxy-6-methylflavone
5-Hydroxy-4,7-dimethoxy-6-methylflavone is found in beverages. 5-Hydroxy-4,7-dimethoxy-6-methylflavone is isolated from Gaultheria procumbens (wintergreen). Isolated from Gaultheria procumbens (wintergreen). 5-Hydroxy-4,7-dimethoxy-6-methylflavone is found in tea, herbs and spices, and beverages.
Cabreuvin
Cabreuvin is isolated from Myroxylon balsamum (Tolu balsam
1,4,5-Trihydroxy-3-prenylxanthone
1,4,5-Trihydroxy-3-prenylxanthone is found in fruits. 1,4,5-Trihydroxy-3-prenylxanthone is a constituent of the root bark of Garcinia livingstonei (imbe). Constituent of the root bark of Garcinia livingstonei (imbe). 1,4,5-Trihydroxy-3-prenylxanthone is found in fruits.
3',4',5'-Trimethoxyflavone
3,4,5-Trimethoxyflavone is found in herbs and spices. 3,4,5-Trimethoxyflavone is a constituent of the flowers of Primula veris (cowslip). Constituent of the flowers of Primula veris (cowslip). 3,4,5-Trimethoxyflavone is found in tea and herbs and spices.
1-[2-(2H-1,3-benzodioxol-5-yl)-1-benzofuran-5-yl]propane-1,3-diol
3',5,6-Trimethoxyflavone
3,5,6-Trimethoxyflavone is found in pomes. 3,5,6-Trimethoxyflavone is isolated from Casimiroa edulis (Mexican apple). Isolated from Casimiroa edulis (Mexican apple). 3,5,6-Trimethoxyflavone is found in pomes.
(±)-Dulciol E
(±)-Dulciol E is found in fruits. (±)-Dulciol E is a constituent of Garcinia dulcis (mundu)
1,3,7-Trihydroxy-2-prenylxanthone
1,3,7-Trihydroxy-2-prenylxanthone is a natural product found in Hypericum chinense, Garcinia forbesii, and other organisms with data available.
Pancixanthone B
A member of the class of xanthones that is a tetracyclic compound 1,2-dihydro-6H-furo[2,3-c]xanthen-6-one substituted by hydroxy groups at positions 5 and 10 and methyl groups at positions 1,1 and 2. It has been isolated from Calophyllum pauciflorum and Garcinia vieillardii.
4-(1,1-Dimethyl-2-propenyl)-1,2,7-trihydroxyxanthone
Sideroxylin
Sideroxylin is a monomethoxyflavone that is flavone substituted by a methoxy group at position 7, hydroxy groups at positions 5 and 4 and methyl groups at positions 6 and 8. It has been isolated from Hydrastis canadensis and Eucalyptus species. It has a role as a plant metabolite. It is a dihydroxyflavone and a monomethoxyflavone. It is functionally related to a flavone. Sideroxylin is a natural product found in Myrtus communis, Hydrastis canadensis, and other organisms with data available. A monomethoxyflavone that is flavone substituted by a methoxy group at position 7, hydroxy groups at positions 5 and 4 and methyl groups at positions 6 and 8. It has been isolated from Hydrastis canadensis and Eucalyptus species.
5,2-Dihydroxy-7-methoxy-6,8-dimethylflavone
5,7,8-Trimethoxyflavone
Norwogonin 5,7,8-trimethyl ether is a natural product found in Uvaria welwitschii with data available.
1,3,5-trihydroxy-8-(3-methylbut-2-enyl)xanthen-9-one
(E)-5,7-dihydroxy-6,8-dimethyl-3-(4-hydroxybenzylidene)chroman-4-one
Tri-Me ether-1,3,7-Trihydroxy-6-methylanthraquinone
(2S)-5,7-Dimethoxy-8-formylflavanone
A dimethoxyflavanone that is 5,7-dimethoxyflavanone substituted by a formyl group at position 8. Isolated from the stem bark of Pongamia pinnata, it acts as a an inducer of quinone reductase, a phase II enzyme that protects cells against reactive, toxic and potentially carcinogenic species.
(2S)-8-formyl-5-hydroxy-7-methoxy-6-methylflavanone
A monohydroxyflavanone that is (2S)-flavanone substituted by a hydroxy group at position 5, a methoxy group at position 7, a methyl group at position 6 and a formyl group at position 8. Isolated from Cleistocalyx operculatus, it has been shown to exhibit inhibitory effects on the viral neuraminidases from two influenza viral strains, H1N1 and H9N2.
1,3,5-trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one
perseal G|rel-(7S,8S)-3-methoxy-3,4-methylenedioxy-7-oxo-8.5,7.O.4-8,9-bisnorneolignan
(E)-7,8-dimethoxy-3-(4-hydroxybenzylidene)chroman-4-one|7,8-dimethoxy-3-(4-hydroxybenzylidene)chroman-4-one|8-methoxybonducellin
2,6-Di-Me ether,Ac-2-(2,4-Dihydroxyphenyl)-6-hydroxybenzofuran|2-(4-acetoxy-2-methoxy-phenyl)-6-methoxy-benzofuran|Vignafuranmonoacetat
Tri-Me ether-1,2,5-Trihydroxy-6-methylanthraquinon
2-Methoxy-3-hydroxy-8,8,10-trimethylanthracene-1,4,5(8H)-trione
3-formyl-4,6-dihydroxy-2-methoxy-5-methyl-chalcone
6a,11a-Dihydro-9-methoxy-6H-benzofuro[3,2-c][1]benzopyran-3-ol acetate
1-Hydroxy-6,8-dimethoxy-2,3-dimethylanthracene-9,10-dione
2-[2-(4-Hydroxyphenyl)ethyl]-6-hydroxy-7-methoxychromone
6-hydroxy-2-[2-(3-methoxy-4-hydroxyphenyl)ethyl]chromone
7-Hydroxy-12-(1-methyl-1-hydroxyethyl)-3,2-(epoxyethano)-9H-xanthene-9-one
(E)-7-hydroxy-3-(2,4-dimethoxybenzylidene)chroman-4-one|2-methoxybonducellin|7-hydroxy-3-(2,4-dimethoxybenzylidene)chroman-4-one
5,8-Dihydroxy-2-(2-(4-methoxyphenyl)ethyl)chromone
2,4,8-trihydroxy-1-(3-methylbut-2-enyl)xanthen-9-one
(-)-sclerodione|(S)-Sclerodione|(??)-Sclerodione|sclerodione
2,6,8-trihydroxy-1-(3-methylbut-2-enyl)xanthen-9-one
7-hydroxy-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-c]xanthen-6-one
ACon1_001643
5,6,7-trimethoxyflavone is a trimethoxyflavone that is the 5,6,7-trimethyl ether derivative of baicalein. It has been isolated from the plant Callicarpa japonica and has been shown to exhibit antiviral activity. It has a role as a plant metabolite and an anti-HSV-1 agent. It is functionally related to a baicalein. 5,6,7-Trimethoxyflavone is a natural product found in Callicarpa japonica, Friesodielsia velutina, and other organisms with data available. A trimethoxyflavone that is the 5,6,7-trimethyl ether derivative of baicalein. It has been isolated from the plant Callicarpa japonica and has been shown to exhibit antiviral activity. 5,6,7-Trimethoxyflavone is a novel p38-α MAPK inhibitor with an anti-inflammatory effect. 5,6,7-Trimethoxyflavone is isolated from several plants including Zeyhera tuberculosa, Callicarpa japonica, and Kickxia lanigera[1]. 5,6,7-Trimethoxyflavone is a novel p38-α MAPK inhibitor with an anti-inflammatory effect. 5,6,7-Trimethoxyflavone is isolated from several plants including Zeyhera tuberculosa, Callicarpa japonica, and Kickxia lanigera[1].
Tanshindiol C
Tanshindiol C is a natural product found in Salvia miltiorrhiza and Salvia miltiorrhiza var. miltiorrhiza with data available.
Tanshindiol A
Tanshindiol A is a natural product found in Salvia miltiorrhiza with data available.
Tanshindiol B
Tanshindiol B is a natural product found in Salvia miltiorrhiza with data available.
3OHX-MB
1,3,5-Trihydroxy-4-(3-methylbut-2-en-1-yl)-9H-xanthen-9-one is a natural product found in Maclura cochinchinensis, Maclura tricuspidata, and Anaxagorea luzonensis with data available.
Baicalein Trimethyl Ether
5,6,7-Trimethoxyflavone is a novel p38-α MAPK inhibitor with an anti-inflammatory effect. 5,6,7-Trimethoxyflavone is isolated from several plants including Zeyhera tuberculosa, Callicarpa japonica, and Kickxia lanigera[1]. 5,6,7-Trimethoxyflavone is a novel p38-α MAPK inhibitor with an anti-inflammatory effect. 5,6,7-Trimethoxyflavone is isolated from several plants including Zeyhera tuberculosa, Callicarpa japonica, and Kickxia lanigera[1].
2,3,6-Trimethoxyflavone
relative retention time with respect to 9-anthracene Carboxylic Acid is 1.289 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.291
3,4-Dimethoxy-3-hydroxy-6-methylflavone
relative retention time with respect to 9-anthracene Carboxylic Acid is 1.320 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.318
5,6-dimethoxy-2-(2-methoxyphenyl)chromen-4-one
(4-formyl-9-methoxy-5-methylbenzo[f][1]benzofuran-3-yl)methyl acetate
C18H16O5_2(5H)-Furanone, 4-(2-hydroxy-4-methoxyphenyl)-5-[(4-hydroxyphenyl)methyl]
1,3,6-trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one
5,6-dimethoxy-2-(2-methoxyphenyl)chromen-4-one [IIN-based on: CCMSLIB00000847313]
5,6-dimethoxy-2-(2-methoxyphenyl)chromen-4-one [IIN-based: Match]
5,7,4-Trimethoxyflavone
5,7,4'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) that is a famous medicinal plant from Thailand. 5,7,4'-Trimethoxyflavone induces apoptosis, as evidenced by increments of sub-G1 phase, DNA fragmentation, annexin-V/PI staining, the Bax/Bcl-xL ratio, proteolytic activation of caspase-3, and degradation of poly (ADP-ribose) polymerase (PARP) protein.5,7,4'-Trimethoxyflavone is significantly effective at inhibiting proliferation of SNU-16 human gastric cancer cells in a concentration dependent manner[1]. 5,7,4'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) that is a famous medicinal plant from Thailand. 5,7,4'-Trimethoxyflavone induces apoptosis, as evidenced by increments of sub-G1 phase, DNA fragmentation, annexin-V/PI staining, the Bax/Bcl-xL ratio, proteolytic activation of caspase-3, and degradation of poly (ADP-ribose) polymerase (PARP) protein.5,7,4'-Trimethoxyflavone is significantly effective at inhibiting proliferation of SNU-16 human gastric cancer cells in a concentration dependent manner[1].
2,4,6-Cycloheptatrien-1-one,3-[3-(3,4-dimethoxyphenyl)-1-oxo-2-propen-1-yl]-2-hydroxy-
Ethyl 5-hydroxy-2-(phenoxymethyl)-1-benzofuran-3-carboxylate
2-(3,4-Dimethoxyphenyl)-3-hydroxy-6-methylchromen-4-one
1-[2-(1,3-Benzodioxol-5-yl)-1-benzouran-5-yl]propane-1,3-diol
(2S)-6-formyl-8-methyl-7-O-methylpinocembrin
A monohydroxyflavanone that is (2S)-flavanone substituted by a hydroxy group at position 5, a methoxy group at position 7, a methyl group at position 8 and a formyl group at position 6. Isolated from the buds of Cleistocalyx operculatus, it has been shown to exhibit inhibitory effects on the viral neuraminidases from two influenza viral strains, H1N1 and H9N2.
5-Hydroxy-7-methoxy-3-(3-methoxyphenyl)-8-methylchromen-4-one
Galangin 3,5,7-trimethyl ether
A trimethoxyflavone that is the 3,5,7-trimethyl ether derivative of galangin.