Chemical Formula: C22H20O8

Chemical Formula C22H20O8

Found 55 metabolite its formula value is C22H20O8

Podophyllotoxone

(5AR,8AR,9R)-9-(3,4,5-TRIMETHOXYPHENYL)-5A,6,8A,9-TETRAHYDROISOBENZOFURANO[5,6-F][1,3]BENZODIOXOLE-5,8-DIONE

C22H20O8 (412.115812)


Podophyllotoxone is a lactone and a lignan. Podophyllotoxone is a natural product found in Diphylleia grayi, Podophyllum peltatum, and other organisms with data available. Podophyllotoxone is isolated from the roots of Dysosma versipellis and has anti-cancer activities.Podophyllotoxone is able to inhibit the tubulin polymerization[1]. Podophyllotoxone is isolated from the roots of Dysosma versipellis and has anti-cancer activities.Podophyllotoxone is able to inhibit the tubulin polymerization[1].

   

aklavinone

(+-)-Aklavinone

C22H20O8 (412.115812)


   

Mollicellin C

Mollicellin C

C22H20O8 (412.115812)


A member of the class of depsidones that is 11H-dibenzo[b,e][1,4]dioxepine substituted by hydroxy groups at positions 3 and 9, a methoxy group at position 8, methyl groups at positions 1 and 6, a 3-methylbut-2-enoyl group at position 7, an oxo group at position 11 and a formyl group at position 4. Isolated from Chaetomium brasiliense, it exhibits antimalarial and cytotoxic activities.

   

Mollicellin C

7,14-dihydroxy-6-methoxy-4,12-dimethyl-5-(3-methylbut-2-enoyl)-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3(8),4,6,12,14-hexaene-15-carbaldehyde

C22H20O8 (412.115812)


Mollicellin C is produced by Chaetomium species and mutagenic mycotoxin. Production by Chaetomium subspecies and mutagenic mycotoxin.

   

Methyl (1R,2R)-2-ethyl-2,5,7,10-tetrahydroxy-6,11-dioxo-3,4-dihydro-1H-tetracene-1-carboxylate

Methyl (1R,2R)-2-ethyl-2,5,7,10-tetrahydroxy-6,11-dioxo-3,4-dihydro-1H-tetracene-1-carboxylic acid

C22H20O8 (412.115812)


   

Peperomin E

4-[bis(7-methoxy-2H-1,3-benzodioxol-5-yl)methyl]-3-methylideneoxolan-2-one

C22H20O8 (412.115812)


   
   
   
   

4alpha-(2,4-Dihydroxy-3-methoxyphenyl)fisetinidol

4alpha-(2,4-Dihydroxy-3-methoxyphenyl)fisetinidol

C22H20O8 (412.115812)


   
   
   

(2E)-5,7-Dihydroxy-3,6-dimethoxy-4-oxo-2-phenyl-4H-1-benzopyran-8-yl ester 2-methyl-2-butenoic acid

(2E)-5,7-Dihydroxy-3,6-dimethoxy-4-oxo-2-phenyl-4H-1-benzopyran-8-yl ester 2-methyl-2-butenoic acid

C22H20O8 (412.115812)


   

4beta-(2,4-Dihydroxy-3-methoxyphenyl)fisetinidol

4beta- (2,4-Dihydroxy-3-methoxyphenyl) fisetinidol

C22H20O8 (412.115812)


   

MCULE-3635034493

MCULE-3635034493

C22H20O8 (412.115812)


   

6abeta,6bbeta,12abeta,12bbeta-Tetrahydro-1,3,7,9-tetramethoxy-6H,12H-cyclobuta[1,2-c:3,4-c]bis[1]benzopyran-6,12-dione

6abeta,6bbeta,12abeta,12bbeta-Tetrahydro-1,3,7,9-tetramethoxy-6H,12H-cyclobuta[1,2-c:3,4-c]bis[1]benzopyran-6,12-dione

C22H20O8 (412.115812)


   

2,3-Di-Me ether,tri-Ac-2,3,4,6,7-Pentahydroxyphenanthrene

2,3-Di-Me ether,tri-Ac-2,3,4,6,7-Pentahydroxyphenanthrene

C22H20O8 (412.115812)


   
   

Dihydro-3-(.alpha.-acetoxypiperonyl)-4-piperonyl-2(3H)-furanone

Dihydro-3-(.alpha.-acetoxypiperonyl)-4-piperonyl-2(3H)-furanone

C22H20O8 (412.115812)


   

(cis-head-to-head)-Limettin dimer

(cis-head-to-head)-Limettin dimer

C22H20O8 (412.115812)


   

3-[(1,3-Benzodioxole-5-yl)methyl]-4-[(1,3-benzodioxole-5-yl)(acetoxy)methyl]tetrahydrofuran-2-one

3-[(1,3-Benzodioxole-5-yl)methyl]-4-[(1,3-benzodioxole-5-yl)(acetoxy)methyl]tetrahydrofuran-2-one

C22H20O8 (412.115812)


   

Dehydroheliobuphthalmin

Dehydroheliobuphthalmin

C22H20O8 (412.115812)


   

1-hydroxycollybolide

1-hydroxycollybolide

C22H20O8 (412.115812)


   

9-hydroxycollybolide

9-hydroxycollybolide

C22H20O8 (412.115812)


   

4-hydroxy-3-methoxy-(S)-mitorubrin

4-hydroxy-3-methoxy-(S)-mitorubrin

C22H20O8 (412.115812)


   

3,5,7-tri-O-acetylhesperetin

3,5,7-tri-O-acetylhesperetin

C22H20O8 (412.115812)


   

epsilon-rhodomycinone

epsilon-rhodomycinone

C22H20O8 (412.115812)


   

5,7,8-trihydroxy-3,6-dimethoxyflavone 8-O-<(E)-2-methyl-2-butenoate>

5,7,8-trihydroxy-3,6-dimethoxyflavone 8-O-<(E)-2-methyl-2-butenoate>

C22H20O8 (412.115812)


   

SCHEMBL11065192

SCHEMBL11065192

C22H20O8 (412.115812)


   

Thuriferic acid

Thuriferic acid

C22H20O8 (412.115812)


   

2-(3-Methoxy-4-acetoxyphenyl)-3-(acetoxymethyl)-7-methoxybenzofuran-5-carbaldehyde

2-(3-Methoxy-4-acetoxyphenyl)-3-(acetoxymethyl)-7-methoxybenzofuran-5-carbaldehyde

C22H20O8 (412.115812)


   

3,5-Dihydroxy-7-(prenyloxy)-8-methoxy-3,4-(methylenebisoxy)flavone

3,5-Dihydroxy-7-(prenyloxy)-8-methoxy-3,4-(methylenebisoxy)flavone

C22H20O8 (412.115812)


   

3-[2,2-bis(7-methoxy-1,3-benzodioxol-5-yl)ethyl]furan-2(5H)-one|peperomin G

3-[2,2-bis(7-methoxy-1,3-benzodioxol-5-yl)ethyl]furan-2(5H)-one|peperomin G

C22H20O8 (412.115812)


   
   

2,3-dimethoxy-5-(2,5-dimethoxy-3,4-methylenedioxyphenyl)-7-methyl-[1,4]-naphthoquinone

2,3-dimethoxy-5-(2,5-dimethoxy-3,4-methylenedioxyphenyl)-7-methyl-[1,4]-naphthoquinone

C22H20O8 (412.115812)


   

1,5,8-Trihydroxy-3-methoxycarbonylmethyl-2-(3-oxopentyl)-9,10-anthraquinone

1,5,8-Trihydroxy-3-methoxycarbonylmethyl-2-(3-oxopentyl)-9,10-anthraquinone

C22H20O8 (412.115812)


   

4-Hydroxy-3-methyl-6,7-(methylenedioxy)-1-(3,4,5-trimethoxyphenyl)-2-naphthoic acid|junaphtoic acid

4-Hydroxy-3-methyl-6,7-(methylenedioxy)-1-(3,4,5-trimethoxyphenyl)-2-naphthoic acid|junaphtoic acid

C22H20O8 (412.115812)


   

SCHEMBL13197634

SCHEMBL13197634

C22H20O8 (412.115812)


   

Aglycone-Feudomycin B

Aglycone-Feudomycin B

C22H20O8 (412.115812)


   

2,3-dimethoxy-6-(2,5-dimethoxy-3,4-methylenedioxyphenyl)-7-methyl-[1,4]-naphthoquinone

2,3-dimethoxy-6-(2,5-dimethoxy-3,4-methylenedioxyphenyl)-7-methyl-[1,4]-naphthoquinone

C22H20O8 (412.115812)


   

xi-Rhodomycinone

xi-Rhodomycinone

C22H20O8 (412.115812)


   

6-hydroxy-3-methoxy-mitorubrin

6-hydroxy-3-methoxy-mitorubrin

C22H20O8 (412.115812)


   

Podophyllotoxone

Furo(3,4:6,7)naphtho(2,3-d)-1,3-dioxole-5,8-dione, 5a,6,8a,9-tetrahydro-9-(3,4,5-trimethoxyphenyl)-, (5aR-(5aalpha,8abeta,9alpha))-

C22H20O8 (412.115812)


d,l-Isopodophyllotoxone is a natural product found in Dysosma aurantiocaulis, Podophyllum peltatum, and other organisms with data available. Podophyllotoxone is isolated from the roots of Dysosma versipellis and has anti-cancer activities.Podophyllotoxone is able to inhibit the tubulin polymerization[1]. Podophyllotoxone is isolated from the roots of Dysosma versipellis and has anti-cancer activities.Podophyllotoxone is able to inhibit the tubulin polymerization[1].

   

Picropodophyllone

Furo(3,4:6,7)naphtho(2,3-d)-1,3-dioxole-5,8-dione, 5a,6,8a,9-tetrahydro-9-(3,4,5-trimethoxyphenyl)-, (5aR-(5aalpha,8aalpha,9aalpha))-

C22H20O8 (412.115812)


Picropodopyllotoxone is a natural product found in Juniperus sabina with data available. Picropodophyllone, an aryltetralin lignan, is isolated from leaves of Podophyllum hexandrum, and has antifungal activities[1][2]. Picropodophyllone, an aryltetralin lignan, is isolated from leaves of Podophyllum hexandrum, and has antifungal activities[1][2].

   

NCGC00380243-01!

NCGC00380243-01!

C22H20O8 (412.115812)


   

2,4,18-trihydroxy-15-(3-hydroxy-3-methylbutyl)-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1(12),2,5,10,14,16,18-heptaen-20-one

2,4,18-trihydroxy-15-(3-hydroxy-3-methylbutyl)-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1(12),2,5,10,14,16,18-heptaen-20-one

C22H20O8 (412.115812)


   

6,8-di-O-methylnidurufin

6,8-di-O-methylnidurufin

C22H20O8 (412.115812)


   

2,4,18-trihydroxy-15-(3-hydroxy-3-methylbutyl)-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1(12),2,5,10,14,16,18-heptaen-20-one_major

2,4,18-trihydroxy-15-(3-hydroxy-3-methylbutyl)-7,9,13-trioxapentacyclo[10.8.0.0³,¹⁰.0⁴,⁸.0¹⁴,¹⁹]icosa-1(12),2,5,10,14,16,18-heptaen-20-one_major

C22H20O8 (412.115812)


   

2,4,18-trihydroxy-15-(3-hydroxy-3-methylbutyl)-7,9,13-trioxapentacyclo[10.8.0.0³,¹?.0?,?.0¹?,¹?]icosa-1(12),2,5,10,14,16,18-heptaen-20-one

2,4,18-trihydroxy-15-(3-hydroxy-3-methylbutyl)-7,9,13-trioxapentacyclo[10.8.0.0³,¹?.0?,?.0¹?,¹?]icosa-1(12),2,5,10,14,16,18-heptaen-20-one

C22H20O8 (412.115812)


   

Austocystin D

Austocystin D

C22H20O8 (412.115812)


An organic heteropentacyclic compound isolated from Aspergillus and Aspergillus ustus and has been shown to exhibit cytotoxic activity. D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D009676 - Noxae > D011042 - Poisons > D000348 - Aflatoxins

   

477-49-6

(5aR,8aR,9R)-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydroisobenzofurano[5,6-f][1,3]benzodioxole-5,8-quinone

C22H20O8 (412.115812)


Podophyllotoxone is isolated from the roots of Dysosma versipellis and has anti-cancer activities.Podophyllotoxone is able to inhibit the tubulin polymerization[1]. Podophyllotoxone is isolated from the roots of Dysosma versipellis and has anti-cancer activities.Podophyllotoxone is able to inhibit the tubulin polymerization[1].

   

Aklavinon

1-Naphthacenecarboxylic acid, 2-ethyl-1,2,3,4,6,11-hexahydro-2,4,5,7-tetrahydroxy-6,11-dioxo-, methyl ester, [1R-(1alpha,2beta,4beta)]-

C22H20O8 (412.115812)


   

2,4,18-Trihydroxy-15-(3-hydroxy-3-methylbutyl)-7,9,13-trioxapentacyclo[10.8.0.03,10.04,8.014,19]icosa-1,3(10),5,11,14,16,18-heptaen-20-one

2,4,18-Trihydroxy-15-(3-hydroxy-3-methylbutyl)-7,9,13-trioxapentacyclo[10.8.0.03,10.04,8.014,19]icosa-1,3(10),5,11,14,16,18-heptaen-20-one

C22H20O8 (412.115812)


   

4-[Bis(7-methoxy-1,3-benzodioxol-5-yl)methyl]-3-methylideneoxolan-2-one

4-[Bis(7-methoxy-1,3-benzodioxol-5-yl)methyl]-3-methylideneoxolan-2-one

C22H20O8 (412.115812)