Chemical Formula: C30H34O6

Chemical Formula C30H34O6

Found 44 metabolite its formula value is C30H34O6

Rubraflavone C

2-(2,4-dihydroxyphenyl)-3-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

C30H34O6 (490.2355264)


Rubraflavone C is found in fruits. Rubraflavone C is a constituent of Morus rubra (red mulberry)

   

Tanariflavanone B

5,7,4-Trihydroxy-6-prenyl-6"-methyl,6"- (4-methylpent-3-enyl) -pyrano [ 2",3":3,2 ] flavanone

C30H34O6 (490.2355264)


A trihydroxyflavanone that consists of (2S)-2,3-dihydro-2H,4H-2,5-bichromen-4-one skeleton substituted by hydroxy groups at positions 5, 7 and 8, a methyl group at position 2, a prenyl group at position 6 and a 4-methylpent-3-enyl group at position 2. Isolated from Macaranga tanarius, it exhibits alleopathic effect.

   
   
   
   

Decathieleanolide

Decathieleanolide

C30H34O6 (490.2355264)


   

Millewanin C

5,7,3,4-Tetrahydroxy-5-((2E)-3,7-dimethyl-2,6-octadienyl)-2-prenylisoflavone

C30H34O6 (490.2355264)


   

Macaflavanone B

(+)-Macaflavanone B

C30H34O6 (490.2355264)


   

Amorinin

5,7,3-Trihydroxy-6,8-di-C-prenyl-6",6"-dimethylpyrano [ 2",3":4,5 ] flavanone

C30H34O6 (490.2355264)


   
   

dorsilurin E

2,(6Z)-6-(3,4,7,8,12,13-Hexahydro-2,2,6,6,13,13-hexamethyl-2H,6H,10H,11H-tripyrano[3,2-c:2,3-f:2,3-h][1]benzopyran-10-ylidene)-3-hydroxy-4-cyclohexadien-1-one

C30H34O6 (490.2355264)


   
   

macaflavanone E

(+)-Macaflavanone E

C30H34O6 (490.2355264)


   

Moralbanone

2- (2,4-Dihydroxyphenyl) -5,7-dihydroxy-8- [ (2E,6E) -3,7,11-trimethyl-2,6,10-dodecatrienyl ] -4H-1-benzopyran-4-one

C30H34O6 (490.2355264)


   

Artocommunol CD

2- (2,4-Dihydroxyphenyl) -3- [ (2E) -3,7-dimethyl-2,6-octadienyl ] -5,7-dihydroxy-8- (3-methyl-2-butenyl) -4H-1-benzopyran-4-one

C30H34O6 (490.2355264)


   

Artelasticin

2- (2,4-Dihydroxyphenyl) -5,7-dihydroxy-3,6,8-tris (3-methyl-2-butenyl) -4H-1-benzopyran-4-one

C30H34O6 (490.2355264)


   

Dorsilurin A

2-[2,4-Dihydroxy-3-(3-methyl-2-butenyl)phenyl]-5,7-dihydroxy-6,8-bis(3-methyl-2-butenyl)-4H-1-benzopyran-4-one

C30H34O6 (490.2355264)


   

Macaflavanone D

(-)-Macaflavanone D

C30H34O6 (490.2355264)


   

Euchrenone b2

5,7,2,4-Tetrahydroxy-6,8,3-triprenylisoflavone

C30H34O6 (490.2355264)


   

Rubraflavone C

2- (2,4-Dihydroxyphenyl) -3- (3,7-dimethyl-2,6-octadienyl) -5,7-dihydroxy-6- (3-methyl-2-butenyl) -4H-1-benzopyran-4-one

C30H34O6 (490.2355264)


   
   

DORSILURIN F

DORSILURIN F

C30H34O6 (490.2355264)


A 7-hydroxyflavonol substituted by additional hydroxy groups at positions 5 and 3 and prenyl groups at positions 6, 8 and 4. Isolated from the roots of Dorstenia psilurus, it exhibits alpha-glucosidase inhibitory activity. D007004 - Hypoglycemic Agents > D065089 - Glycoside Hydrolase Inhibitors D004791 - Enzyme Inhibitors

   

DORSILURIN K

DORSILURIN K

C30H34O6 (490.2355264)


An extended flavonoid that is flavonol with an additional hydroxy group at position 3, two 2,2-dimethyldihydropyrano rings fused to ring A across positions 5, 6 and 7, 8 respectively and a prenyl group at position 4. Isolated from the roots of Dorstenia psilurus, it exhibits alpha-glucosidase inhibitory activity.

   

DORSILURIN J

DORSILURIN J

C30H34O6 (490.2355264)


An extended flavonoid that is 7-hydroxyflavonol with an additional hydroxy group at position 3, a 2,2-dimethyldihydropyrano ring fused to ring A across positions 5 and 6, and prenyl groups at positions 8 and 4. Isolated from the roots of Dorstenia psilurus, it exhibits alpha-glucosidase inhibitory activity.

   

1-[5,7-dihydroxy-2-methyl-6-(3-methylbut-2-enyl)-2-(4-methylpent-3-enyl)chromen-8-yl]-3-(3,4-dihydroxyphenyl)prop-2-en-1-one

1-[5,7-dihydroxy-2-methyl-6-(3-methylbut-2-enyl)-2-(4-methylpent-3-enyl)chromen-8-yl]-3-(3,4-dihydroxyphenyl)prop-2-en-1-one

C30H34O6 (490.2355264)


   

(+)-7,7-bis[(5R,7R,9R,10S)-2-oxocadinan-3,6(11)-dien-12,7-olide]

(+)-7,7-bis[(5R,7R,9R,10S)-2-oxocadinan-3,6(11)-dien-12,7-olide]

C30H34O6 (490.2355264)


   

5,7,2,4-tetrahydroxy-3-geranyl-8-prenylflavone|artocommunol CD

5,7,2,4-tetrahydroxy-3-geranyl-8-prenylflavone|artocommunol CD

C30H34O6 (490.2355264)


   

(2S)-5,2,4-trihydroxy-8,5-di(3-methylbut-2-enyl)-6,7-(3,3-dimethylpyrano)flavanone

(2S)-5,2,4-trihydroxy-8,5-di(3-methylbut-2-enyl)-6,7-(3,3-dimethylpyrano)flavanone

C30H34O6 (490.2355264)


   
   

3-(3,4-dihydroxyphenyl)-1-[6-(3,7-dimethylocta-2,6-dienyl)-5,7-dihydroxy-2,2-dimethylchromen-8-yl]prop-2-en-1-one

3-(3,4-dihydroxyphenyl)-1-[6-(3,7-dimethylocta-2,6-dienyl)-5,7-dihydroxy-2,2-dimethylchromen-8-yl]prop-2-en-1-one

C30H34O6 (490.2355264)


   

8-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one|moralbanone

8-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one|moralbanone

C30H34O6 (490.2355264)


   
   

kadcoccilactone L

kadcoccilactone L

C30H34O6 (490.2355264)


   
   

5,7,3-trihydroxy-4,5-(2,2-dimethylpyran)-8,2-di(3-methyl-2-butenyl)-(2S)-flavanone

5,7,3-trihydroxy-4,5-(2,2-dimethylpyran)-8,2-di(3-methyl-2-butenyl)-(2S)-flavanone

C30H34O6 (490.2355264)


An extended flavonoid that consists of (2S)-flavanone substituted by hydroxy groups at positions 5, 7 and 3, prenyl groups at positions 8 and 2 and a gem-dimethyl pyran ring fused across positions 4 and 5. Isolated from Dendrolobium lanceolatum, it exhibits antimalarial activity.

   

3-Geranyl-3-prenyl-5,7,2,4-tetrahydroxyflavone

2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxyphenyl]-5,7-dihydroxy-3-(3-methylbut-2-enyl)chromen-4-one

C30H34O6 (490.2355264)


   

3,5,6-tri-O-.benzyl-1,2-O-isopropylidene-alpha-D-glucofuranose

3,5,6-tri-O-.benzyl-1,2-O-isopropylidene-alpha-D-glucofuranose

C30H34O6 (490.2355264)


   

rac-(2E)-1-[5,7-dihydroxy-2-methyl-6-(3-methylbut-2-en-1-yl)-2-(4-methylpent-3-en-1-yl)-2H-chromen-8-yl]-3-(3,4-dihydroxyphenyl)prop-2-en-1-one

rac-(2E)-1-[5,7-dihydroxy-2-methyl-6-(3-methylbut-2-en-1-yl)-2-(4-methylpent-3-en-1-yl)-2H-chromen-8-yl]-3-(3,4-dihydroxyphenyl)prop-2-en-1-one

C30H34O6 (490.2355264)


   

Mallotophilippen D

Mallotophilippen D

C30H34O6 (490.2355264)


A member of the class of chalcones that is chalcone substituted by hydroxy groups at positions 3, 4, 2 and 4, a geranyl group at position 3 and a 6,6-dimethyl-3,6-dihydro-2H-pyran ring fused across positions 5 and 6. Isolated from the fruits of Mallotus philippensis, it exhibits anti-inflammatory and immunoregulatory activities.

   

(R)-mallotophilippen E

(R)-mallotophilippen E

C30H34O6 (490.2355264)


The (R)-enantiomer of mallotophilippen E.

   

(S)-mallotophilippen E

(S)-mallotophilippen E

C30H34O6 (490.2355264)


The (S)-enantiomer of mallotophilippen E.

   

(RS)-mallotophilippen E

(RS)-mallotophilippen E

C30H34O6 (490.2355264)


A racemate composed of equimolar quantities of R- and S- mallotophilippen E. Isolated from the fruits of Mallotus philippensis, it exhibits anti-inflammatory and immunoregulatory activities.

   

mallotophilippen E

mallotophilippen E

C30H34O6 (490.2355264)


A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 3, 4, 2 and 4, a prenyl group at position 3 and a 6-methyl-6-(4-methylpent-3-en-1-yl)-3,6-dihydro-2H-pyran ring fused across positions 5 and 6