Chemical Formula: C30H34O5

Chemical Formula C30H34O5

Found 28 metabolite its formula value is C30H34O5

Rubraflavone B

2-(2,4-dihydroxyphenyl)-3-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-7-hydroxy-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

C30H34O5 (474.24061140000003)


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

   

Poinsettifolin B

1- (2,4-Dihydroxy-3-prenylphenyl) -3- [ 2-methyl-2- (4-methyl-3-pentenyl) -8-hydroxy-2H-1-benzopyran-5-yl ] -2-propene-1-one

C30H34O5 (474.24061140000003)


   

Millewanin D

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

C30H34O5 (474.24061140000003)


   
   

Euchrenone a4

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

C30H34O5 (474.24061140000003)


   

Flemiphyllin

5,7,4-Trihydroxy-8,3,5-triprenylisoflavone

C30H34O5 (474.24061140000003)


   

Euchrenone b1

5,7,4-Trihydroxy-6,8,3-triprenylisoflavone

C30H34O5 (474.24061140000003)


   

5,7,4-trihydroxy-6,8-di(3-methylbut-2-enyl)-3-(1,1-dimethylallyl)isoflavone|fleminginin

5,7,4-trihydroxy-6,8-di(3-methylbut-2-enyl)-3-(1,1-dimethylallyl)isoflavone|fleminginin

C30H34O5 (474.24061140000003)


   

1-[6-(3,7-dimethylocta-2,6-dienyl)-5,7-dihydroxy-2,2-dimethyl-2H-chromen-8-yl]-3-(4-hydroxyphenyl)propenone|mallotophilippen C

1-[6-(3,7-dimethylocta-2,6-dienyl)-5,7-dihydroxy-2,2-dimethyl-2H-chromen-8-yl]-3-(4-hydroxyphenyl)propenone|mallotophilippen C

C30H34O5 (474.24061140000003)


   

5,7,4-trihydroxy-8,2,5-tri(3-methylbut-2-enyl)isoflavanone|strobiliferyllin

5,7,4-trihydroxy-8,2,5-tri(3-methylbut-2-enyl)isoflavanone|strobiliferyllin

C30H34O5 (474.24061140000003)


   

(2S)-5,7-dihydroxy-3,8-di(3-methyl-2-enyl)-2,2-dimethylpyrano[5,6:5,4]flavanone|maackiaflavanone B

(2S)-5,7-dihydroxy-3,8-di(3-methyl-2-enyl)-2,2-dimethylpyrano[5,6:5,4]flavanone|maackiaflavanone B

C30H34O5 (474.24061140000003)


   
   

5,7-dihydroxy-8-(2-methylbutanoyl)-6-[(E)-3,7-dimethylocta-2,6-dienyl]-4-phenyl-2H-chromen-2-one

5,7-dihydroxy-8-(2-methylbutanoyl)-6-[(E)-3,7-dimethylocta-2,6-dienyl]-4-phenyl-2H-chromen-2-one

C30H34O5 (474.24061140000003)


   

1,8,10-trihydroxy-6-methyl-4,5-bis-(3,3-dimethylallyl)-2,3-(2,2-dimethylpyrano)anthrone|kenganthranol E

1,8,10-trihydroxy-6-methyl-4,5-bis-(3,3-dimethylallyl)-2,3-(2,2-dimethylpyrano)anthrone|kenganthranol E

C30H34O5 (474.24061140000003)


   
   
   
   

5,7-dihydroxy-6-(3-methylbutanoyl)-8-[(E)-3,7-dimethylocta-2,6-dienyl]-4-phenyl-2H-chromen-2-one

5,7-dihydroxy-6-(3-methylbutanoyl)-8-[(E)-3,7-dimethylocta-2,6-dienyl]-4-phenyl-2H-chromen-2-one

C30H34O5 (474.24061140000003)


   
   

5,7-dihydroxy-8-(3-methylbutanoyl)-6-[(E)-3,7-dimethylocta-2,6-dienyl]-4-phenyl-2H-chromen-2-one

5,7-dihydroxy-8-(3-methylbutanoyl)-6-[(E)-3,7-dimethylocta-2,6-dienyl]-4-phenyl-2H-chromen-2-one

C30H34O5 (474.24061140000003)


   

5,7-dihydroxy-6-(2-methylbutanoyl)-8-[(E)-3,7-dimethylocta-2,6-dienyl]-4-phenyl-2H-chromen-2-one

5,7-dihydroxy-6-(2-methylbutanoyl)-8-[(E)-3,7-dimethylocta-2,6-dienyl]-4-phenyl-2H-chromen-2-one

C30H34O5 (474.24061140000003)


   
   

Guajadial F

1,3-Dihydroxy-5a,10-dimethyl-12-phenyl-7-propan-2-yl-7,8,9,10,10a,11,11a,12-octahydrobenzo[b]xanthene-2,4-dicarbaldehyde

C30H34O5 (474.24061140000003)


   
   
   

Maackiaflavanone B

Maackiaflavanone B

C30H34O5 (474.24061140000003)


A dihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 5 and 7, prenyl groups at positions 8 and 3 and a 6,6-dimethyl-3,6-dihydro-2H-pyran ring fused across positions 4 and 5. Isolated from the stem barks of Maackia amurensis, it exhibits cytotoxicity against human cancer cell lines.

   

Mallotophilippen C

Mallotophilippen C

C30H34O5 (474.24061140000003)


A member of the class of chalcones that is chalcone substituted by hydroxy groups at positions 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.