NCBI Taxonomy: 1643356

Pityrogramma ebenea (ncbi_taxid: 1643356)

found 31 associated metabolites at species taxonomy rank level.

Ancestor: Pityrogramma

Child Taxonomies: none taxonomy data.

Genkwanin

5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-chromen-4-one

C16H12O5 (284.0685)


Genkwanin, also known as 5,4-dihydroxy-7-methoxyflavone or 7-methylapigenin, is a member of the class of compounds known as 7-o-methylated flavonoids. 7-o-methylated flavonoids are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Thus, genkwanin is considered to be a flavonoid lipid molecule. Genkwanin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Genkwanin is a bitter tasting compound and can be found in a number of food items such as winter savory, sweet basil, rosemary, and common sage, which makes genkwanin a potential biomarker for the consumption of these food products. Genkwanin is an O-methylated flavone, a type of flavonoid. It can be found in the seeds of Alnus glutinosa, and the leaves of the ferns Notholaena bryopoda and Asplenium normale . Genkwanin is a major non-glycosylated flavonoid with anti-flammatory activities. Genkwanin is a major non-glycosylated flavonoid with anti-flammatory activities.

   

Sakuranetin

4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-, (2S)-

C16H14O5 (286.0841)


Sakuranetin is a flavonoid phytoalexin that is (S)-naringenin in which the hydroxy group at position 7 is replaced by a methoxy group. It has a role as an antimycobacterial drug and a plant metabolite. It is a dihydroxyflavanone, a monomethoxyflavanone, a flavonoid phytoalexin, a member of 4-hydroxyflavanones and a (2S)-flavan-4-one. It is functionally related to a (S)-naringenin. Sakuranetin is a natural product found in Ageratina altissima, Chromolaena odorata, and other organisms with data available. Sakuranetin is found in black walnut. Sakuranetin is a flavanone, a type of flavonoid. It can be found in Polymnia fruticosa and rice, where it acts as a phytoalexin against spore germination of Pyricularia oryzae Sakuranetin is a flavanone, a type of flavonoid. It can be found in Polymnia fruticosa and rice, where it acts as a phytoalexin against spore germination of Pyricularia oryzae. A flavonoid phytoalexin that is (S)-naringenin in which the hydroxy group at position 7 is replaced by a methoxy group. Sakuranetin is a cherry flavonoid phytoalexin, shows strong antifungal activity[1]. Sakuranetin has anti-inflammatory and antioxidative activities. Sakuranetin ameliorates LPS-induced acute lung injury[2]. Sakuranetin is a cherry flavonoid phytoalexin, shows strong antifungal activity[1]. Sakuranetin has anti-inflammatory and antioxidative activities. Sakuranetin ameliorates LPS-induced acute lung injury[2].

   

Rhamnocitrin

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one

C16H12O6 (300.0634)


Rhamnocitrin, also known as 3,4,5-trihydroxy-7-methoxyflavone or 7-methylkaempferol, is a member of the class of compounds known as flavonols. Flavonols are compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position. Thus, rhamnocitrin is considered to be a flavonoid lipid molecule. Rhamnocitrin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Rhamnocitrin can be found in cloves and lemon balm, which makes rhamnocitrin a potential biomarker for the consumption of these food products. Rhamnocitrin is a monomethoxyflavone that is the 7-methyl ether derivative of kaempferol. It has a role as a plant metabolite. It is a trihydroxyflavone, a member of flavonols and a monomethoxyflavone. It is functionally related to a kaempferol. Rhamnocitrin is a natural product found in Ageratina altissima, Chromolaena odorata, and other organisms with data available. Hydroxygenkwanin (7-O-Methylluteolin), a natural flavonoid compound, is one of the main components of Lilac Daphne. Hydroxygenkwanin has anti-oxidant ability, anti-glioma ability and anticancer effect[1][2]. Hydroxygenkwanin (7-O-Methylluteolin), a natural flavonoid compound, is one of the main components of Lilac Daphne. Hydroxygenkwanin has anti-oxidant ability, anti-glioma ability and anticancer effect[1][2]. Rhamnocitrin is a flavonoid isolated from astragalus complanatus R. Br. (Sha-yuan-zi)[1]. Rhamnocitrin is a scavenger of DPPH with an IC50 of 28.38 mM. Rhamnocitrin has anti-oxidant, anti-inflammatory and an-tiatherosclerosis activity[2]. Rhamnocitrin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=569-92-6 (retrieved 2024-12-30) (CAS RN: 569-92-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

Pinostrobin

(2R)-5-hydroxy-7-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one

C16H14O4 (270.0892)


A monohydroxyflavanone that is (2S)-flavanone substituted by a hydroxy group at position 5 and a methoxy group at position 7 respectively. Pinostrobin is a natural product found in Uvaria chamae, Zuccagnia punctata, and other organisms with data available.

   

Genkwanin

4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-

C16H12O5 (284.0685)


Genkwanin is a monomethoxyflavone that is apigenin in which the hydroxy group at position 7 is methylated. It has a role as a metabolite. It is a dihydroxyflavone and a monomethoxyflavone. It is functionally related to an apigenin. It is a conjugate acid of a genkwanin(1-). Genkwanin is a natural product found in Odontites viscosus, Eupatorium capillifolium, and other organisms with data available. A monomethoxyflavone that is apigenin in which the hydroxy group at position 7 is methylated. Genkwanin is a major non-glycosylated flavonoid with anti-flammatory activities. Genkwanin is a major non-glycosylated flavonoid with anti-flammatory activities.

   

Pinostrobin chalcone

2-Propen-1-one, 1-(2,6-dihydroxy-4-methoxyphenyl)-3-phenyl-, (E)-; Chalcone, 2,6-dihydroxy-4-methoxy- ; 2,6-Dihydroxy-4-methoxychalcone

C16H14O4 (270.0892)


Pinostrobin chalcone is a member of chalcones. Pinostrobin chalcone is a natural product found in Onychium siliculosum, Populus koreana, and other organisms with data available. Pinostrobin chalcone is found in pulses. Pinostrobin chalcone is isolated from Cajanus cajan (pigeon pea). Isolated from Cajanus cajan (pigeon pea). Pinostrobin chalcone is found in pulses. Pinostrobin chalcone is found to be potent natural cytotoxic compounds against MDA-MB-231 and HT-29 colon cancer cell lines(IC50 = 20.42±2.23 and 22.51±0.42 μg/mL)[1]. Pinostrobin chalcone is found to be potent natural cytotoxic compounds against MDA-MB-231 and HT-29 colon cancer cell lines(IC50 = 20.42±2.23 and 22.51±0.42 μg/mL)[1].

   

(2E)-1-(2,6-dihydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one

(2E)-1-(2,6-dihydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one

C16H14O5 (286.0841)


   

Calomelanone

Calomelanone

C17H18O5 (302.1154)


   

(E)-2,6-Dihydroxy-4,4-dimethoxychalcone

(E)-2,6-Dihydroxy-4,4-dimethoxychalcone

C17H16O5 (300.0998)


   

(2R)-5-Hydroxy-7-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one

(2R)-5-hydroxy-7-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one

C16H14O4 (270.0892)


Pinostrobin, also known as 5-hydroxy-7-methoxyflavanone, is a member of the class of compounds known as 7-o-methylated flavonoids. 7-o-methylated flavonoids are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. Thus, pinostrobin is considered to be a flavonoid lipid molecule. Pinostrobin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Pinostrobin can be found in a number of food items such as roman camomile, soursop, rocket salad, and angelica, which makes pinostrobin a potential biomarker for the consumption of these food products.

   

Calomelanol D

(-) -9,10-Dihydro-3,5-dihydroxy-2- (4-hydroxyphenyl) -10-phenyl-4H,8H-benzo [ 1,2-b:3,4-b ] dipyran-4,8-dione

C24H16O7 (416.0896)


   

Calomelanol H

3,4,7,8-Tetrahydro-5-hydroxy-8- (4-hydroxyphenyl) -4-phenyl-2H,6H-benzo [ 1,2-b:5,4-b ] dipyran-2,6-dione

C24H18O6 (402.1103)


   

Calomelanol D-1

3,4-Dihydro-5,7-dihydroxy-4-phenyl-8- (3-phenyl-1-oxopropyl) -2H-1-benzopyran-2-one

C24H20O5 (388.1311)


   

Calomelanone

2,6-DIHYDROXY-4,4-DIMETHOXYDIHYDROCHALCONE

C17H18O5 (302.1154)


   

Gymnogrammene

2,6-Dihydroxy-4,4-dimethoxychalcone

C17H16O5 (300.0998)


   

Genkwanin

4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-

C16H12O5 (284.0685)


Genkwanin is a major non-glycosylated flavonoid with anti-flammatory activities. Genkwanin is a major non-glycosylated flavonoid with anti-flammatory activities.

   

Rhamnocitrin

4H-1-Benzopyran-4-one, 3,5-dihydroxy-2-(4-hydroxyphenyl)-7-methoxy-

C16H12O6 (300.0634)


Rhamnocitrin is a monomethoxyflavone that is the 7-methyl ether derivative of kaempferol. It has a role as a plant metabolite. It is a trihydroxyflavone, a member of flavonols and a monomethoxyflavone. It is functionally related to a kaempferol. Rhamnocitrin is a natural product found in Ageratina altissima, Chromolaena odorata, and other organisms with data available. A monomethoxyflavone that is the 7-methyl ether derivative of kaempferol. Hydroxygenkwanin (7-O-Methylluteolin), a natural flavonoid compound, is one of the main components of Lilac Daphne. Hydroxygenkwanin has anti-oxidant ability, anti-glioma ability and anticancer effect[1][2]. Hydroxygenkwanin (7-O-Methylluteolin), a natural flavonoid compound, is one of the main components of Lilac Daphne. Hydroxygenkwanin has anti-oxidant ability, anti-glioma ability and anticancer effect[1][2]. Rhamnocitrin is a flavonoid isolated from astragalus complanatus R. Br. (Sha-yuan-zi)[1]. Rhamnocitrin is a scavenger of DPPH with an IC50 of 28.38 mM. Rhamnocitrin has anti-oxidant, anti-inflammatory and an-tiatherosclerosis activity[2]. Rhamnocitrin is a flavonoid isolated from astragalus complanatus R. Br. (Sha-yuan-zi)[1]. Rhamnocitrin is a scavenger of DPPH with an IC50 of 28.38 mM. Rhamnocitrin has anti-oxidant, anti-inflammatory and an-tiatherosclerosis activity[2].

   

Sakuranetin

(S) -2,3-Dihydro-5-hydroxy-2- (4-hydroxyphenyl) -7-methoxy-4H-1-benzopyran-4-one

C16H14O5 (286.0841)


Annotation level-1 Sakuranetin is a cherry flavonoid phytoalexin, shows strong antifungal activity[1]. Sakuranetin has anti-inflammatory and antioxidative activities. Sakuranetin ameliorates LPS-induced acute lung injury[2]. Sakuranetin is a cherry flavonoid phytoalexin, shows strong antifungal activity[1]. Sakuranetin has anti-inflammatory and antioxidative activities. Sakuranetin ameliorates LPS-induced acute lung injury[2].

   

Pinocembrin-7-methyl ether

5-hydroxy-7-methoxy-2-phenylchroman-4-one

C16H14O4 (270.0892)


   

(10s)-3,5-dihydroxy-2-(4-hydroxyphenyl)-10-phenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

(10s)-3,5-dihydroxy-2-(4-hydroxyphenyl)-10-phenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

C24H16O7 (416.0896)


   

5-hydroxy-8-(4-hydroxyphenyl)-4-phenyl-3h,4h-pyrano[3,2-g]chromene-2,6-dione

5-hydroxy-8-(4-hydroxyphenyl)-4-phenyl-3h,4h-pyrano[3,2-g]chromene-2,6-dione

C24H16O6 (400.0947)


   

(2s)-7-hydroxy-5-methoxy-2-(4-methoxyphenyl)-2,3-dihydro-1-benzopyran-4-one

(2s)-7-hydroxy-5-methoxy-2-(4-methoxyphenyl)-2,3-dihydro-1-benzopyran-4-one

C17H16O5 (300.0998)


   

1-(4,6-dihydroxy-7-methoxy-2h-1,3-benzodioxol-5-yl)-3-(4-methoxyphenyl)propan-1-one

1-(4,6-dihydroxy-7-methoxy-2h-1,3-benzodioxol-5-yl)-3-(4-methoxyphenyl)propan-1-one

C18H18O7 (346.1052)


   

(4s)-5-hydroxy-8-(4-hydroxyphenyl)-4-phenyl-3h,4h-pyrano[3,2-g]chromene-2,6-dione

(4s)-5-hydroxy-8-(4-hydroxyphenyl)-4-phenyl-3h,4h-pyrano[3,2-g]chromene-2,6-dione

C24H16O6 (400.0947)


   

5-hydroxy-2,10-diphenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

5-hydroxy-2,10-diphenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

C24H16O5 (384.0998)


   

1-(2,6-dihydroxy-4-methoxyphenyl)-3-(3,4-dimethoxyphenyl)propan-1-one

1-(2,6-dihydroxy-4-methoxyphenyl)-3-(3,4-dimethoxyphenyl)propan-1-one

C18H20O6 (332.126)


   

(10s)-5-hydroxy-2-(4-hydroxyphenyl)-10-phenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

(10s)-5-hydroxy-2-(4-hydroxyphenyl)-10-phenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

C24H16O6 (400.0947)


   

5-hydroxy-2-(4-hydroxyphenyl)-10-phenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

5-hydroxy-2-(4-hydroxyphenyl)-10-phenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

C24H16O6 (400.0947)


   

(10s)-5-hydroxy-2,10-diphenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

(10s)-5-hydroxy-2,10-diphenyl-9h,10h-pyrano[2,3-h]chromene-4,8-dione

C24H16O5 (384.0998)


   

(4s)-5,7-dihydroxy-4-phenyl-8-(3-phenylpropanoyl)-3,4-dihydro-1-benzopyran-2-one

(4s)-5,7-dihydroxy-4-phenyl-8-(3-phenylpropanoyl)-3,4-dihydro-1-benzopyran-2-one

C24H20O5 (388.1311)


   

(4r)-5,7-dihydroxy-4-phenyl-8-(3-phenylpropanoyl)-3,4-dihydro-1-benzopyran-2-one

(4r)-5,7-dihydroxy-4-phenyl-8-(3-phenylpropanoyl)-3,4-dihydro-1-benzopyran-2-one

C24H20O5 (388.1311)