Chemical Formula: C21H23NO6

Chemical Formula C21H23NO6

Found 47 metabolite its formula value is C21H23NO6

Polycarpine

(1Z)-1-[(2-hydroxy-3,4-dimethoxyphenyl)methylidene]-6,7-dimethoxy-3,4-dihydroisoquinoline-2-carbaldehyde

C21H23NO6 (385.1525298)


   

Gloriosine

Formamide,N-[(7S)-5,6,7,9-tetrahydro-1,2,3,10-tetramethoxy-9-oxobenzo[a]heptalen-7-yl]-

C21H23NO6 (385.1525298)


   

N-Methylporphyroxine

11,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14,16,18-hexaen-16-ol

C21H23NO6 (385.1525298)


N-Methylporphyroxine is an alkaloid from Papaver somniferum (opium poppy

   

Papaverrubine B

11,16,17-trimethoxy-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14,16,18-hexaene

C21H23NO6 (385.1525298)


Papaverrubine B is found in opium poppy. Papaverrubine B is an alkaloid from Papaver rhoeas (corn poppy

   

Glaucamine

16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]docosa-2(10),3,5(9),14,16,18-hexaen-11-ol

C21H23NO6 (385.1525298)


Glaucamine is an alkaloid from Papaver rhoeas (corn poppy

   

Romucosine H

Methyl 3-hydroxy-4,15,16-trimethoxy-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(17),2(7),3,5,13,15-hexaene-10-carboxylic acid

C21H23NO6 (385.1525298)


Romucosine H is found in cherimoya. Romucosine H is an alkaloid from Annona cherimola (cherimoya).

   

3-Desmethylcolchicine

N-{5-hydroxy-3,4,14-trimethoxy-13-oxotricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl}ethanimidate

C21H23NO6 (385.1525298)


   

Colchiceine

N-{14-hydroxy-3,4,5-trimethoxy-13-oxotricyclo[9.5.0.0²,⁷]hexadeca-1(16),2(7),3,5,11,14-hexaen-10-yl}acetamide

C21H23NO6 (385.1525298)


   

3-Demethylcolchicine

3-Demethylcolchicine

C21H23NO6 (385.1525298)


3-Demethylcolchicine, a colchicine metabolite, possesses a hydroxy-group on its carbon ring that could participate in radical scavenging and markedly inhibits the carrageenin edema[1][2]. 3-Demethylcolchicine, a colchicine metabolite, possesses a hydroxy-group on its carbon ring that could participate in radical scavenging and markedly inhibits the carrageenin edema[1][2].

   

2-Demethylcolchicine

(-)-2-Demethylcolchicine

C21H23NO6 (385.1525298)


   
   

N-Methylporphyroxine

11,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0^{2,10}.0^{5,9}.0^{14,19}]docosa-2,4,9,14(19),15,17-hexaen-16-ol

C21H23NO6 (385.1525298)


   

4-Hydroxycanadaline

4-Hydroxycanadaline

C21H23NO6 (385.1525298)


   

N-Methoxycarbonyllaurotetanine

N-Methoxycarbonyllaurotetanine

C21H23NO6 (385.1525298)


   

(13S,14R)-1,13-dihydroxy-N-methylcanadine

(13S,14R)-1,13-dihydroxy-N-methylcanadine

C21H23NO6 (385.1525298)


   
   
   
   

Colchicine, O(3)-demethyl-

Colchicine, O(3)-demethyl-

C21H23NO6 (385.1525298)


   

O(sup 2)-Demethylcolchicine

O(sup 2)-Demethylcolchicine

C21H23NO6 (385.1525298)


   

(7bR)-7t-Acetylamino-2-hydroxy-1,3,9-trimethoxy-(7br,10ac)-6,7,7b,10a-tetrahydro-5H-benzo[a]cyclopenta[3,4]-cyclobuta[1,2-c]cyclohepten-8-on|(7bR)-7t-acetylamino-2-hydroxy-1,3,9-trimethoxy-(7br,10ac)-6,7,7b,10a-tetrahydro-5H-benzo[a]cyclopenta[3,4]-cyclobuta[1,2-c]cyclohepten-8-one|O2-De-Me-beta-Lumicolchicine

(7bR)-7t-Acetylamino-2-hydroxy-1,3,9-trimethoxy-(7br,10ac)-6,7,7b,10a-tetrahydro-5H-benzo[a]cyclopenta[3,4]-cyclobuta[1,2-c]cyclohepten-8-on|(7bR)-7t-acetylamino-2-hydroxy-1,3,9-trimethoxy-(7br,10ac)-6,7,7b,10a-tetrahydro-5H-benzo[a]cyclopenta[3,4]-cyclobuta[1,2-c]cyclohepten-8-one|O2-De-Me-beta-Lumicolchicine

C21H23NO6 (385.1525298)


   
   
   

(+-)-aryapavine|11-hydroxy-12-hydroxymethyl-1,10-dimethoxy-2,3-methylenedioxyberbine|12-hydroxymethyl-10,14-dimethoxy-5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinolin-11-ol|12-Hydroxymethylprotoberberin|Aryapavin|Aryapavine

(+-)-aryapavine|11-hydroxy-12-hydroxymethyl-1,10-dimethoxy-2,3-methylenedioxyberbine|12-hydroxymethyl-10,14-dimethoxy-5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinolin-11-ol|12-Hydroxymethylprotoberberin|Aryapavin|Aryapavine

C21H23NO6 (385.1525298)


   

(+)-N-(methoxycarbonyl)-N-norpredicentrine

(+)-N-(methoxycarbonyl)-N-norpredicentrine

C21H23NO6 (385.1525298)


   

2-Desmethyl-beta-lumicolchicin|O2-Demethyl-beta-lumicolchicin|O3-De-Me-beta-Lumicolchicine

2-Desmethyl-beta-lumicolchicin|O2-Demethyl-beta-lumicolchicin|O3-De-Me-beta-Lumicolchicine

C21H23NO6 (385.1525298)


   

(+)-N-(methoxy-carbonyl)-N-norlauroscholtzine

(+)-N-(methoxy-carbonyl)-N-norlauroscholtzine

C21H23NO6 (385.1525298)


   
   

(-)-8-oxo-11-hydroxy-2,3,9,10-tetramethoxyberberine

(-)-8-oxo-11-hydroxy-2,3,9,10-tetramethoxyberberine

C21H23NO6 (385.1525298)


   
   

(+)-chelamidine|chelamidine

(+)-chelamidine|chelamidine

C21H23NO6 (385.1525298)


   

(S)-4,9,10,11-tetramethoxy-6,7,7a,8-tetrahydro-5H-benzo[g][1,3]dioxolo[4,5:4,5]benzo[1,2,3-de]quinoline|Nor-Leucoxylonin|Norleucoxylonine

(S)-4,9,10,11-tetramethoxy-6,7,7a,8-tetrahydro-5H-benzo[g][1,3]dioxolo[4,5:4,5]benzo[1,2,3-de]quinoline|Nor-Leucoxylonin|Norleucoxylonine

C21H23NO6 (385.1525298)


   

Buntanmine A|buntanmine-A

Buntanmine A|buntanmine-A

C21H23NO6 (385.1525298)


   

(+)-ocoxylonine|(S)-4,10,11-trimethoxy-7-methyl-6,7,7a,8-tetrahydro-5H-benzo[g][1,3]dioxolo[4,5:4,5]benzo[1,2,3-de]quinolin-9-ol|Ocoxylonin|Ocoxylonine

(+)-ocoxylonine|(S)-4,10,11-trimethoxy-7-methyl-6,7,7a,8-tetrahydro-5H-benzo[g][1,3]dioxolo[4,5:4,5]benzo[1,2,3-de]quinolin-9-ol|Ocoxylonin|Ocoxylonine

C21H23NO6 (385.1525298)


   

6-hydroxy-allocryptopine

6-hydroxy-allocryptopine

C21H23NO6 (385.1525298)


   

NCI60_001400

N-[(7S,12aRa)-3-Hydroxy-1,2,10-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl]acetamide (3-O-Demethylcolchicine)

C21H23NO6 (385.1525298)


3-Desmethylcolchicine is a natural product found in Colchicum arenarium, Colchicum bivonae, and other organisms with data available. 3-Demethylcolchicine, a colchicine metabolite, possesses a hydroxy-group on its carbon ring that could participate in radical scavenging and markedly inhibits the carrageenin edema[1][2]. 3-Demethylcolchicine, a colchicine metabolite, possesses a hydroxy-group on its carbon ring that could participate in radical scavenging and markedly inhibits the carrageenin edema[1][2].

   

Desmethylcolchicine

Desmethylcolchicine

C21H23NO6 (385.1525298)


3-Demethylcolchicine, a colchicine metabolite, possesses a hydroxy-group on its carbon ring that could participate in radical scavenging and markedly inhibits the carrageenin edema[1][2]. 3-Demethylcolchicine, a colchicine metabolite, possesses a hydroxy-group on its carbon ring that could participate in radical scavenging and markedly inhibits the carrageenin edema[1][2].

   
   

Glaucamine

16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.0^{2,10}.0^{5,9}.0^{14,19}]docosa-2,4,9,14(19),15,17-hexaen-11-ol

C21H23NO6 (385.1525298)


   

Papaverrubine B

11,16,17-trimethoxy-6,8,12-trioxa-22-azapentacyclo[11.9.0.0^{2,10}.0^{5,9}.0^{14,19}]docosa-2,4,9,14,16,18-hexaene

C21H23NO6 (385.1525298)


   

Romucosine H

methyl 3-hydroxy-4,15,16-trimethoxy-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,13(17),14-hexaene-10-carboxylate

C21H23NO6 (385.1525298)


   

2-Demethyl Colchicine-d3

2-Demethyl Colchicine-d3

C21H23NO6 (385.1525298)


   

Fmoc-8-amino-3,6-dioxaoctanoic acid

Fmoc-8-amino-3,6-dioxaoctanoic acid

C21H23NO6 (385.1525298)


   

7-Acetamido-10-hydroxy-1,2,3-trimethoxy-6,7-dihydrobenzo[a]heptalen-9(5H)-one

7-Acetamido-10-hydroxy-1,2,3-trimethoxy-6,7-dihydrobenzo[a]heptalen-9(5H)-one

C21H23NO6 (385.1525298)


   

(7S)-7-acetamido-1,2,3-trimethoxy-6,7-dihydro-5H-dibenzo[5,3-b:1,2-e][7]annulene-9-carboxylic acid

(7S)-7-acetamido-1,2,3-trimethoxy-6,7-dihydro-5H-dibenzo[5,3-b:1,2-e][7]annulene-9-carboxylic acid

C21H23NO6 (385.1525298)


   

(1Z)-1-[(2-hydroxy-3,4-dimethoxyphenyl)methylidene]-6,7-dimethoxy-3,4-dihydroisoquinoline-2-carbaldehyde

(1Z)-1-[(2-hydroxy-3,4-dimethoxyphenyl)methylidene]-6,7-dimethoxy-3,4-dihydroisoquinoline-2-carbaldehyde

C21H23NO6 (385.1525298)