Chemical Formula: C25H24O6

Chemical Formula C25H24O6

Found 101 metabolite its formula value is C25H24O6

Pomiferin

3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-en-1-yl)-4H,8H-pyrano[2,3-h]chromen-4-one

C25H24O6 (420.1572804)


   

Morusin

4H,8H-BENZO(1,2-B:3,4-B)DIPYRAN-4-ONE, 2-(2,4-DIHYDROXYPHENYL)-5-HYDROXY-8,8-DIMETHYL-3-(3-METHYL-2-BUTEN-1-YL)-

C25H24O6 (420.1572804)


Morusin is an extended flavonoid that is flavone substituted by hydroxy groups at positions 5, 2 and 4, a prenyl group at position 3 and a 2,2-dimethyl pyran group across positions 7 and 8. It has a role as a plant metabolite and an antineoplastic agent. It is a trihydroxyflavone and an extended flavonoid. Morusin is a natural product found in Morus alba var. multicaulis, Broussonetia papyrifera, and other organisms with data available. An extended flavonoid that is flavone substituted by hydroxy groups at positions 5, 2 and 4, a prenyl group at position 3 and a 2,2-dimethyl pyran group across positions 7 and 8. Morusin is found in fruits. Morusin is a constituent of the root bark of Morus alba (mulberry) and other Morus species Constituent of the root bark of Morus alba (mulberry) and other Morus subspecies Morusin is found in fruits. Morusin is a prenylated flavonoid isolated from Morus alba Linn. with various biological activities, such as antitumor, antioxidant, and anti-bacteria property. Morusin could inhibit NF-κB and STAT3 activity. Morusin is a prenylated flavonoid isolated from Morus alba Linn. with various biological activities, such as antitumor, antioxidant, and anti-bacteria property. Morusin could inhibit NF-κB and STAT3 activity.

   

Pomiferin

4H,8H-BENZO(1,2-B:3,4-B)DIPYRAN-4-ONE, 3-(3,4-DIHYDROXYPHENYL)-5-HYDROXY-8,8-DIMETHYL-6-(3-METHYL-2-BUTEN-1-YL)-

C25H24O6 (420.1572804)


Pomiferin is a member of isoflavanones. Pomiferin is a natural product found in Derris montana, Maclura pomifera, and other organisms with data available.

   

Kuwanon A

4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(5-hydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl)-3-(3-methyl-2-buten-1-yl)-

C25H24O6 (420.1572804)


Kuwanon A is a member of flavones. Kuwanon A is a natural product found in Morus alba var. multicaulis, Morus lhou, and Morus alba with data available. Kuwanon A is found in fruits. Kuwanon A is a constituent of the root bark of Morus alba (white mulberry) Kuwanon A is a flavone derivative isolated from the root barks of the mulberry tree (Morus alba L.); inhibits nitric oxide production with an IC50 of 10.5 μM. Kuwanon A is a flavone derivative isolated from the root barks of the mulberry tree (Morus alba L.); inhibits nitric oxide production with an IC50 of 10.5 μM.

   

Kuwanon B

5,7-Dihydroxy-2-(5-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-3-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one, 9CI

C25H24O6 (420.1572804)


Kuwanon B is a member of flavones. Kuwanon B is a natural product found in Morus alba with data available. Kuwanon B is found in fruits. Kuwanon B is a constituent of the root bark of Morus alba (white mulberry)

   

Cyclocommunin

(E)-(+)-3,8,10-Trihydroxy-9-(3-methyl-1-butenyl)-6-(2-methyl-1-propenyl)-6H,7H-[1]benzopyrano[4,3-b][1]benzopyran-7-one

C25H24O6 (420.1572804)


Cyclocommunin is found in fruits. Cyclocommunin is isolated from the rootbark of Artocarpus communis and stems of Artocarpus altilis (breadfruit). Isolated from the rootbark of Artocarpus communis and stems of Artocarpus altilis (breadfruit). Cyclocommunin is found in fruits.

   

Cyclomulberrin

3,8,10-Trihydroxy-11-(3-methyl-2-butenyl)-6-(2-methyl-1-propenyl)-6H,7H-[1]benzopyrano[4,3-b][1]benzopyran-7-one, 9ci

C25H24O6 (420.1572804)


Cyclomulberrin is found in fruits. Cyclomulberrin is isolated from the bark of Morus species Also isolated from Artocarpus altilis (breadfruit

   
   

Acetyl blancoxanthone

Acetyl blancoxanthone

C25H24O6 (420.1572804)


   

Shanciol

trans- (-) -3,4,5,6-Tetrahydro-2- (4-hydroxy-3-methoxyphenyl) -11-methoxy-2H-phenanthro [ 2,1-b ] pyran-3,8-diol

C25H24O6 (420.1572804)


   

Yinyanghuo A

(-)-5,7-Dihydroxy-2-[8-(2-hydroxy-3-methyl-3-butenyl)-2,2-dimethyl-2H-1-benzopyran-6-yl]-4H-1-benzopyran-4-one

C25H24O6 (420.1572804)


An extended flavonoid that is 2,2-dimethyl-2H,4H-2,6-bichromen-4-one substituted by hydroxy groups at positions 5 and 7 and a 2-hydroxy-3-methylbut-3-en-1-yl group at position 8. Isolated from Epimedium sagittatum, it exhibits inhibitory activity against platelet aggregation.

   

Australone A

2H, (-) -8- (2,4-Dihydroxyphenyl) -5-hydroxy-2-methyl-2- (4-methyl-3-pentenyl) -6H-benzo [ 1,2-b:5,4-b ] dipyran-6-one

C25H24O6 (420.1572804)


   

Isocyclomulberrin

(+) -3,8,10-Trihydroxy-9- (3-methyl-2-butenyl) -6- (2-methyl-1-propenyl) -6H,7H- [ 1 ] benzopyrano [ 4,3-b ] [ 1 ] benzopyran-7-one

C25H24O6 (420.1572804)


   

Calophyllic acid

[ Z, (-) ] -3- (3,4-Dihydro-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2H,8H-benzo [ 1,2-b:3,4-b ] dipyran-6-yl) -3-phenylpropenoic acid

C25H24O6 (420.1572804)


   

Ulexone C

5-Hydroxy-8- (2-hydroxypropan-2-yl) -3- (2,2-dimethyl-2H-1-benzopyran-6-yl) -8,9-dihydro-4H-furo [ 2,3-h ] -1-benzopyran-4-one

C25H24O6 (420.1572804)


   
   
   
   

6,7] isoflavone

5,4-Dihydroxy-8-(3-methylbut-2-enyl)-2-(4-hydroxy-4-methylethyl) furano[4,5

C25H24O6 (420.1572804)


   

Glyasperin N

5,7,4-Trihydroxy-8-prenyl-6,6-dimethylpyrano[2,3:2,3]isoflavone

C25H24O6 (420.1572804)


   

dehydrolupinifolinol

dehydrolupinifolinol

C25H24O6 (420.1572804)


   

Lespedezol A6

3,8,9-Trihydroxy-10-(3,7-dimethyl-2,6-octadienyl)coumestan

C25H24O6 (420.1572804)


   

Lespedezol C1

7,4,5-Trihydroxy-3-(3,7-dimethyl-2.,6-octadienyl)coumaronochromone

C25H24O6 (420.1572804)


   

Ficusin B

5,4,7-Trihydroxy-7-methyl-4-(1-methylethenyl)-3a,4,5,6,7,7a-hexahydrobenzofurano[2,3:7,8]isoflavone

C25H24O6 (420.1572804)


   

Kraussianone 2

5,7,2-Trihydroxy-6-prenyl-6,6-dimethylpyrano[2,3:4,5]isoflavone

C25H24O6 (420.1572804)


   
   
   

Ulexin A

5,7-Dihydroxy-6-(2-hydroxy-3-methyl-3-butenyl)-6,6-dimethylpyrano[2,3:4,3]isoflavone

C25H24O6 (420.1572804)


   

Sanggenol O

(2S)-5,7-Dihydroxy-bis(6,6-dimethylpyrano[2,3:2,3][2,3:4,5]flavanone

C25H24O6 (420.1572804)


   

Angustone B

5,7,2-Trihydroxy-6-prenyl-6,6-dimethylpyrano[2,3:4,3]isoflavone

C25H24O6 (420.1572804)


   

Gancaonin H

5,7-dihydroxy-3-(8-hydroxy-2,2-dimethyl-chromen-6-yl)-6-(3-methylbut-2-enyl)chromen-4-one

C25H24O6 (420.1572804)


   

Angustone C

5,2,4-Trihydroxy-3-prenyl-6",6"-dimethylpyrano [ 2",3":7,6 ] isoflavone

C25H24O6 (420.1572804)


   

Macaflavone I

3,3,4-Trihydroxy-6",6"-dimethyl-8-prenylpyrano [ 2,3:7,6 ] flavone

C25H24O6 (420.1572804)


   

Cudraisoflavone A

7- (3,4-Dihydroxyphenyl) -5-hydroxy-2,2-dimethyl-10- (3-methyl-2-butenyl) -2H,6H-benzo [ 1,2-b:5,4-b ] dipyran-6-one

C25H24O6 (420.1572804)


   

Cudraflavone B

8-(2,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-7-(3-methylbut-2-en-1-yl)-2H,6H-pyrano[3,2-g]chromen-6-one

C25H24O6 (420.1572804)


Cudraflavone B is an extended flavonoid that consists of a pyranochromane skeleton that is 2H,6H-pyrano[3,2-g]chromen-6-one substituted by geminal methyl groups at position 2, a 2,4-dihydroxyphenyl group at position 8, a hydroxy group at position 5 and a prenyl group at position 7. Isolated from Morus alba and Morus species it exhibits anti-inflammatory activity. It has a role as an anti-inflammatory agent and a plant metabolite. It is an extended flavonoid, a pyranochromane and a trihydroxyflavone. cudraflavone B is a natural product found in Artocarpus altilis, Maclura tricuspidata, and other organisms with data available. An extended flavonoid that consists of a pyranochromane skeleton that is 2H,6H-pyrano[3,2-g]chromen-6-one substituted by geminal methyl groups at position 2, a 2,4-dihydroxyphenyl group at position 8, a hydroxy group at position 5 and a prenyl group at position 7. Isolated from Morus alba and Morus species it exhibits anti-inflammatory activity.

   
   

AURICULATIN

7- (2,4-Dihydroxyphenyl) -5-hydroxy-2,2-dimethyl-10- (3-methyl-2-butenyl) -2H,6H-benzo [ 1,2-b:5,4-b ] dipyran-6-one

C25H24O6 (420.1572804)


   

Isoauriculatin

5-Hydroxy-7- [ 2-hydroxy-4- [ (3-methyl-2-butenyl) oxy ] phenyl ] -2,2-dimethyl-2H,6H-benzo [ 1,2-b:5,4-b ] dipyran-6-one

C25H24O6 (420.1572804)


   

Isoauriculasin

5-Hydroxy-7- [ 3-hydroxy-4- [ (3-methyl-2-butenyl) oxy ] phenyl ] -2,2-dimethyl-2H,6H-benzo [ 1,2-b:5,4-b ] dipyran-6-one

C25H24O6 (420.1572804)


   

Lupinalbin F

5,7,4-Trihydroxy-6,3-diprenylcoumaronochromone

C25H24O6 (420.1572804)


   

Brosimone I

(E) - (+) -3,8,10-Trihydroxy-9- (3-methyl-1-butenyl) -6- (2-methyl-1-propenyl) -6H,7H- [ 1 ] benzopyrano [ 4,3-b ] [ 1 ] benzopyran-7-one

C25H24O6 (420.1572804)


   

Cyclomulberrin

3,8,10-Trihydroxy-11- (3-methyl-2-butenyl) -6- (2-methyl-1-propenyl) -6H,7H- [ 1 ] benzopyrano [ 4,3-b ] [ 1 ] benzopyran-7-one

C25H24O6 (420.1572804)


A extended flavonoid that is 6H,7H-chromeno[4,3-b]chromen-7-one which is substituted by a 2-methylprop-1-en-1-yl group at position 6, a 3-methylbut-2-en-1-yl group at position 11, and hydroxy groups at positions 3, 8, and 10. It is found in the bark of Morus species and has been reported to protect human neuronal cells derived from the human neuroblastoma SH-SY5Y cell line.

   

Kuwanon A

5,7-Dihydroxy-2- (5-hydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl) -3- (3-methyl-2-butenyl) -4H-1-benzopyran-4-one

C25H24O6 (420.1572804)


Kuwanon A is a flavone derivative isolated from the root barks of the mulberry tree (Morus alba L.); inhibits nitric oxide production with an IC50 of 10.5 μM. Kuwanon A is a flavone derivative isolated from the root barks of the mulberry tree (Morus alba L.); inhibits nitric oxide production with an IC50 of 10.5 μM.

   

Morusin

2- (2,4-Dihydroxyphenyl) -5-hydroxy-8,8-dimethyl-3- (3-methyl-2-butenyl) -4H,8H-benzo [ 1,2-b:3,4-b ] dipyran-4-one

C25H24O6 (420.1572804)


Morusin is a prenylated flavonoid isolated from Morus alba Linn. with various biological activities, such as antitumor, antioxidant, and anti-bacteria property. Morusin could inhibit NF-κB and STAT3 activity. Morusin is a prenylated flavonoid isolated from Morus alba Linn. with various biological activities, such as antitumor, antioxidant, and anti-bacteria property. Morusin could inhibit NF-κB and STAT3 activity.

   

Pomiferin

3- (3,4-Dihydroxyphenyl) -5-hydroxy-8,8-dimethyl-6- (3-methyl-2-butenyl) -4H,8H-benzo [ 1,2-b:3,4-b ] dipyran-4-one

C25H24O6 (420.1572804)


   
   

Lupinisoflavone K

Lupinisoflavone K

C25H24O6 (420.1572804)


   

Acetylblancoxanthone

Acetylblancoxanthone

C25H24O6 (420.1572804)


   

LPGFEBXRFJLODR-UHFFFAOYSA-

LPGFEBXRFJLODR-UHFFFAOYSA-

C25H24O6 (420.1572804)


   

OCHROCARPIN B

OCHROCARPIN B

C25H24O6 (420.1572804)


A furanocoumarin that is 2H-furo[2,3-h]chromen-2-one substituted by a hydroxy group at position 5, 2-hydroxypropan-2-yl group at position 8, a 3-methylbutanoyl group at position 6 and a phenyl group at position 4. Isolated from the bark of Ochrocarpos punctatus, it exhibits cytotoxicity against the A2780 ovarian cancer cell line.

   

6,7-(2,2-dimethylpyrano)-8-prenyl-5,3,4-trihydroxyflavone|ficubee B

6,7-(2,2-dimethylpyrano)-8-prenyl-5,3,4-trihydroxyflavone|ficubee B

C25H24O6 (420.1572804)


   

7,8-(2,2-dimethylpyrano)-6-prenyl-5,3,4-trihydroxyflavone|ficubee A

7,8-(2,2-dimethylpyrano)-6-prenyl-5,3,4-trihydroxyflavone|ficubee A

C25H24O6 (420.1572804)


   
   

5-Hydroxy-3-(8-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-8,8-dimethyl-2H,8H-benzo[1,2-b:5,4-b]dipyran-4(3H)-one

5-Hydroxy-3-(8-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-8,8-dimethyl-2H,8H-benzo[1,2-b:5,4-b]dipyran-4(3H)-one

C25H24O6 (420.1572804)


   

Erysenegalensein G

Erysenegalensein G

C25H24O6 (420.1572804)


   

2(S)-5,7-dihydroxy-[(5,6:3,4)-(2,2-dimethylpyrano)-(5,6:5,6)]-(2,2-dimethylpyrano)flavanone

2(S)-5,7-dihydroxy-[(5,6:3,4)-(2,2-dimethylpyrano)-(5,6:5,6)]-(2,2-dimethylpyrano)flavanone

C25H24O6 (420.1572804)


   
   
   
   

Prenylcandidusin A

Prenylcandidusin A

C25H24O6 (420.1572804)


A member of the class of dibenzofurans that is candidusin A substituted by a prenyl group at position 3 of the phenyl ring substituent. It has been isolated from Aspergillus taichungensis.

   

6,7,-(2,2-dimethylpyrano)-5,4-dihydroxy-3-(3,3-dimethylallyloxy)flavone|afzelin B

6,7,-(2,2-dimethylpyrano)-5,4-dihydroxy-3-(3,3-dimethylallyloxy)flavone|afzelin B

C25H24O6 (420.1572804)


   
   
   

4,2,6-trihydroxy-3-(4-hydroxycinnamyl)-4-methoxydihydrochalcone|balsacone A

4,2,6-trihydroxy-3-(4-hydroxycinnamyl)-4-methoxydihydrochalcone|balsacone A

C25H24O6 (420.1572804)


   

2,4,6-trihydroxy-3-(4-hydroxycinnamyl)-4-methoxydihydrochalcone|balsacone B

2,4,6-trihydroxy-3-(4-hydroxycinnamyl)-4-methoxydihydrochalcone|balsacone B

C25H24O6 (420.1572804)


   

(2,3-trans)-2-(4-hydroxy-3-methoxyphenyl)-3-hydroxymethyl-10-methoxy-2,3,4,5-tetrahydrophenanthro[2,1-b]furan-7-ol

(2,3-trans)-2-(4-hydroxy-3-methoxyphenyl)-3-hydroxymethyl-10-methoxy-2,3,4,5-tetrahydrophenanthro[2,1-b]furan-7-ol

C25H24O6 (420.1572804)


   

(-)-balsacone E|8-(4-methoxydihydrocinnamoyl)-5,7,4?-trihydroxyflavan|balsacone E

(-)-balsacone E|8-(4-methoxydihydrocinnamoyl)-5,7,4?-trihydroxyflavan|balsacone E

C25H24O6 (420.1572804)


   
   
   

5-Hydroxy-6-(4-hydroxy-3-methylbutyryl)-2,2-dimethyl-10-phenyl-2H,8H-benzo[1,2-b:3,4-b]dipyran-8-one

5-Hydroxy-6-(4-hydroxy-3-methylbutyryl)-2,2-dimethyl-10-phenyl-2H,8H-benzo[1,2-b:3,4-b]dipyran-8-one

C25H24O6 (420.1572804)


   
   
   

dihydroartoindonesianin C

dihydroartoindonesianin C

C25H24O6 (420.1572804)


   
   

3-(4-Hydroxyphenyl)-5-hydroxy-8-(hydroxymethyl)-8-methyl-10-prenyl-4H,8H-benzo[1,2-b:5,4-b]dipyran-4-one

3-(4-Hydroxyphenyl)-5-hydroxy-8-(hydroxymethyl)-8-methyl-10-prenyl-4H,8H-benzo[1,2-b:5,4-b]dipyran-4-one

C25H24O6 (420.1572804)


   

3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one

NCGC00013053-07!3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one

C25H24O6 (420.1572804)


   

7-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one

NCGC00384963-01!7-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one

C25H24O6 (420.1572804)


   

3-(2,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one

NCGC00381079-01!3-(2,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one

C25H24O6 (420.1572804)


   

7-(2,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one

NCGC00384972-01!7-(2,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one

C25H24O6 (420.1572804)


   

3-(2,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one

3-(2,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one

C25H24O6 (420.1572804)


   

3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one [IIN-based on: CCMSLIB00000848635]

NCGC00013053-07!3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one [IIN-based on: CCMSLIB00000848635]

C25H24O6 (420.1572804)


   

7-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one [IIN-based: Match]

NCGC00384963-01!7-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one [IIN-based: Match]

C25H24O6 (420.1572804)


   

3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one [IIN-based: Match]

NCGC00013053-07!3-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one [IIN-based: Match]

C25H24O6 (420.1572804)


   

7-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one [IIN-based on: CCMSLIB00000847417]

NCGC00384963-01!7-(3,4-dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one [IIN-based on: CCMSLIB00000847417]

C25H24O6 (420.1572804)


   
   

3-(2,4-Dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methyl-2-buten-1-yl)-4H,8H-pyrano[2,3-f]chromen-4-one

3-(2,4-Dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methyl-2-buten-1-yl)-4H,8H-pyrano[2,3-f]chromen-4-one

C25H24O6 (420.1572804)


   

Ochrocarpin A

Ochrocarpin A

C25H24O6 (420.1572804)


A furanocoumarin that is 2H-furo[2,3-h]chromen-2-one substituted by a hydroxy group at position 5, 2-hydroxypropan-2-yl group at position 8, a 2-methylbutanoyl group at position 6 and a phenyl group at position 4. Isolated from the bark of Ochrocarpos punctatus, it exhibits cytotoxicity against the A2780 ovarian cancer cell line.

   
   

(3s,4s)-3-(4-hydroxy-3-methoxyphenyl)-11-methoxy-2h,3h,4h,5h,6h-phenanthro[2,1-b]pyran-4,8-diol

(3s,4s)-3-(4-hydroxy-3-methoxyphenyl)-11-methoxy-2h,3h,4h,5h,6h-phenanthro[2,1-b]pyran-4,8-diol

C25H24O6 (420.1572804)


   

(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

C25H24O6 (420.1572804)


   

5,7,8'-trihydroxy-2',2'-dimethyl-8-(3-methylbut-2-en-1-yl)-[2,6'-bichromen]-4-one

5,7,8'-trihydroxy-2',2'-dimethyl-8-(3-methylbut-2-en-1-yl)-[2,6'-bichromen]-4-one

C25H24O6 (420.1572804)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-en-1-yl)pyrano[2,3-f]chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-6-(3-methylbut-2-en-1-yl)pyrano[2,3-f]chromen-4-one

C25H24O6 (420.1572804)


   

5,7-dihydroxy-8'-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-2',2'-dimethyl-[2,6'-bichromen]-4-one

5,7-dihydroxy-8'-[(2r)-2-hydroxy-3-methylbut-3-en-1-yl]-2',2'-dimethyl-[2,6'-bichromen]-4-one

C25H24O6 (420.1572804)


   

1-[13-(3-acetyl-4-hydroxybenzoyl)-10-hydroxy-10,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2,4,6-tetraen-4-yl]ethanone

1-[13-(3-acetyl-4-hydroxybenzoyl)-10-hydroxy-10,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2,4,6-tetraen-4-yl]ethanone

C25H24O6 (420.1572804)


   

(3r,4s)-3-(4-hydroxy-3-methoxyphenyl)-11-methoxy-2h,3h,4h,5h,6h-phenanthro[2,1-b]pyran-4,8-diol

(3r,4s)-3-(4-hydroxy-3-methoxyphenyl)-11-methoxy-2h,3h,4h,5h,6h-phenanthro[2,1-b]pyran-4,8-diol

C25H24O6 (420.1572804)


   

5,7-dihydroxy-2-{2,2,9,9-tetramethylpyrano[3,2-h]chromen-5-yl}-2,3-dihydro-1-benzopyran-4-one

5,7-dihydroxy-2-{2,2,9,9-tetramethylpyrano[3,2-h]chromen-5-yl}-2,3-dihydro-1-benzopyran-4-one

C25H24O6 (420.1572804)


   

5,7,7'-trihydroxy-2',2'-dimethyl-6-(3-methylbut-2-en-1-yl)-[3,6'-bichromen]-4-one

5,7,7'-trihydroxy-2',2'-dimethyl-6-(3-methylbut-2-en-1-yl)-[3,6'-bichromen]-4-one

C25H24O6 (420.1572804)


   

1,3,8-trihydroxy-2-(3-methylbut-1-en-1-yl)-11-(2-methylprop-1-en-1-yl)-11h-5,10-dioxatetraphen-12-one

1,3,8-trihydroxy-2-(3-methylbut-1-en-1-yl)-11-(2-methylprop-1-en-1-yl)-11h-5,10-dioxatetraphen-12-one

C25H24O6 (420.1572804)


   

5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one

5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one

C25H24O6 (420.1572804)


   

8,13-dihydroxy-5-(4-hydroxyphenyl)-13-methyl-16-(prop-1-en-2-yl)-3,11-dioxatetracyclo[8.7.0.0²,⁷.0¹²,¹⁷]heptadeca-1,4,7,9-tetraen-6-one

8,13-dihydroxy-5-(4-hydroxyphenyl)-13-methyl-16-(prop-1-en-2-yl)-3,11-dioxatetracyclo[8.7.0.0²,⁷.0¹²,¹⁷]heptadeca-1,4,7,9-tetraen-6-one

C25H24O6 (420.1572804)