Exact Mass: 456.109

Exact Mass Matches: 456.109

Found 78 metabolites which its exact mass value is equals to given mass value 456.109, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Flavin mononucleotide

{[(2R,3S,4S)-5-{7,8-dimethyl-2,4-dioxo-2H,3H,4H,10H-benzo[g]pteridin-10-yl}-2,3,4-trihydroxypentyl]oxy}phosphonic acid

C17H21N4O9P (456.1046)


Flavin mononucleotide, also known as riboflavin 5-monophosphate or riboflavine dihydrogen phosphate, is a member of the class of compounds known as flavin nucleotides. Flavin nucleotides are nucleotides containing a flavin moiety. Flavin is a compound that contains the tricyclic isoalloxazine ring system, which bears 2 oxo groups at the 2- and 4-positions. Flavin mononucleotide is practically insoluble (in water) and a moderately acidic compound (based on its pKa). Flavin mononucleotide can be found in a number of food items such as spinach, elliotts blueberry, tea leaf willow, and black mulberry, which makes flavin mononucleotide a potential biomarker for the consumption of these food products. Flavin mononucleotide can be found primarily in blood, as well as throughout most human tissues. Flavin mononucleotide exists in all living species, ranging from bacteria to humans. In humans, flavin mononucleotide is involved in several metabolic pathways, some of which include riboflavin metabolism, pyrimidine metabolism, beta-alanine metabolism, and doxorubicin metabolism pathway. Flavin mononucleotide is also involved in several metabolic disorders, some of which include beta ureidopropionase deficiency, UMP synthase deficiency (orotic aciduria), carnosinuria, carnosinemia, and hypophosphatasia. Moreover, flavin mononucleotide is found to be associated with anorexia nervosa. Flavin mononucleotide (FMN), or riboflavin-5′-phosphate, is a biomolecule produced from riboflavin (vitamin B2) by the enzyme riboflavin kinase and functions as prosthetic group of various oxidoreductases including NADH dehydrogenase as well as cofactor in biological blue-light photo receptors. During the catalytic cycle, a reversible interconversion of the oxidized (FMN), semiquinone (FMNH•) and reduced (FMNH2) forms occurs in the various oxidoreductases. FMN is a stronger oxidizing agent than NAD and is particularly useful because it can take part in both one- and two-electron transfers. In its role as blue-light photo receptor, (oxidized) FMN stands out from the conventional photo receptors as the signaling state and not an E/Z isomerization . Flavin mononucleotide (FMN), or riboflavin-5′-phosphate, is a biomolecule produced from riboflavin (vitamin B2) by the enzyme riboflavin kinase and functions as the prosthetic group of various oxidoreductases, including NADH dehydrogenase, as well as cofactor in biological blue-light photo receptors. During the catalytic cycle, a reversible interconversion of the oxidized (FMN), semiquinone (FMNH), and reduced (FMNH2) forms occurs in the various oxidoreductases. FMN is a stronger oxidizing agent than NAD and is particularly useful because it can take part in both one- and two-electron transfers. In its role as blue-light photo receptor, (oxidized) FMN stands out from the conventional photo receptors as the signaling state and not an E/Z isomerization. It is the principal form in which riboflavin is found in cells and tissues. It requires more energy to produce, but is more soluble than riboflavin. Flavin mononucleotide belongs to the class of organic compounds known as flavin nucleotides. These are nucleotides containing a flavin moiety. Flavin is a compound that contains the tricyclic isoalloxazine ring system, which bears 2 oxo groups at the 2- and 4-positions. Flavin mononucleotide exists in all living species, ranging from bacteria to humans. Within humans, flavin mononucleotide participates in a number of enzymatic reactions. In particular, formic acid and flavin mononucleotide can be biosynthesized from FMNH2; which is catalyzed by the enzyme lanosterol 14-alpha demethylase. In addition, formic acid and flavin mononucleotide can be biosynthesized from FMNH2 through the action of the enzyme lanosterol 14-alpha demethylase. In humans, flavin mononucleotide is involved in bloch pathway (cholesterol biosynthesis). Outside of the human body, flavin mononucleotide has been detected, but not quantified in several different foods, such as mandarin orange (clementine, tangerine), horseradish tree, black elderberries, angelica, and ostrich ferns. Acquisition and generation of the data is financially supported in part by CREST/JST. D018977 - Micronutrients > D014815 - Vitamins

   

Epicatechin 3-O-(4-methylgallate)

(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,5-dihydroxy-4-methoxybenzoate

C23H20O10 (456.1056)


Epicatechin 3-(4-methylgallate) is a member of the class of compounds known as catechin gallates. Catechin gallates are organic compounds containing a gallate moiety glycosidically linked to a catechin. Thus, epicatechin 3-(4-methylgallate) is considered to be a flavonoid lipid molecule. Epicatechin 3-(4-methylgallate) is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Epicatechin 3-(4-methylgallate) can be found in tea, which makes epicatechin 3-(4-methylgallate) a potential biomarker for the consumption of this food product. Epicatechin 3-O-(4-methylgallate) is found in tea. Epicatechin 3-O-(4-methylgallate) is isolated from Camellia sinensis var. assamica (commercial oolong tea).

   

Epicatechin 3-O-(3-O-methylgallate)

(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4-dihydroxy-5-methoxybenzoate

C23H20O10 (456.1056)


Epicatechin 3-O-(3-O-methylgallate) is found in tea. Epicatechin 3-O-(3-O-methylgallate) is isolated from green China tea (Camellia sinensis) leaves. Isolated from green China tea (Camellia sinensis) leaves. Epicatechin 3-(3-methylgallate) is found in tea.

   

Pinnatifinoside D

Pinnatifinoside D

C23H20O10 (456.1056)


   
   

3,5,7-Tris(acetyloxy)-8-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one

3,5,7-Tris (acetyloxy) -8-methoxy-2- (4-methoxyphenyl) -4H-1-benzopyran-4-one

C23H20O10 (456.1056)


   

Epigallocatechin 3-O-vanillate

(2R,3R) -3,5,7,3,4,5-Hexahydroxyflavan 3-O-vanillate

C23H20O10 (456.1056)


   

Epicatechin 3-O-(4-O-methylgallate)

(2R,3R) -3,5,7,3,4-Pentahydroxyflavan 3-O- (4-O-methylgallate)

C23H20O10 (456.1056)


   
   
   

11-(2-bromo-3,6-dimethoxyphenyl)-3,3-dimethyl-2,3,4-trihydro-5H,10H,11H-benzo[ b]benzo[2,1-f]1,4-diazepin-1-one

11-(2-bromo-3,6-dimethoxyphenyl)-3,3-dimethyl-2,3,4-trihydro-5H,10H,11H-benzo[ b]benzo[2,1-f]1,4-diazepin-1-one

C23H25BrN2O3 (456.1048)


relative retention time with respect to 9-anthracene Carboxylic Acid is 1.125 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.123 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.128 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.127

   

5-epi-bromo-Z-punagladin-3

5-epi-bromo-Z-punagladin-3

C21H29BrO6 (456.1147)


   
   

10-Hydroxy,aglycone-Sulfurmycin A

10-Hydroxy,aglycone-Sulfurmycin A

C23H20O10 (456.1056)


   

Tri-Ac-4,5,7-Trihydroxy-3,3-dimethoxyflavone

Tri-Ac-4,5,7-Trihydroxy-3,3-dimethoxyflavone

C23H20O10 (456.1056)


   

4,5,7-Triacetoxy-3,6-dimethoxy-flavon (synth. Jaceosidin-triacetat)|5,7,4-Triacetoxy-3,6-dimethoxy-flavon|5,7,4-Triacetoxy-6,3-dimethoxy-flavon|5,7-diacetoxy-2-(4-acetoxy-3-methoxy-phenyl)-6-methoxy-chromen-4-one|Jaceosidin-acetat|Jaceosidin-triacetat

4,5,7-Triacetoxy-3,6-dimethoxy-flavon (synth. Jaceosidin-triacetat)|5,7,4-Triacetoxy-3,6-dimethoxy-flavon|5,7,4-Triacetoxy-6,3-dimethoxy-flavon|5,7-diacetoxy-2-(4-acetoxy-3-methoxy-phenyl)-6-methoxy-chromen-4-one|Jaceosidin-acetat|Jaceosidin-triacetat

C23H20O10 (456.1056)


   

4-O-methyl-(-)-epigallocatechin

4-O-methyl-(-)-epigallocatechin

C23H20O10 (456.1056)


   

Eriodictyol tetraacetate

Eriodictyol tetraacetate

C23H20O10 (456.1056)


   

(-)-epicatechin gallate-4-O-Me|4-O-methyl-(-)-epicatechin gallate|4-O-methylepicatechin-3-O-gallate

(-)-epicatechin gallate-4-O-Me|4-O-methyl-(-)-epicatechin gallate|4-O-methylepicatechin-3-O-gallate

C23H20O10 (456.1056)


   

4,6-Dimethoxy-3,5,7-tri-O-acetyl-flavon|5,7-diacetoxy-2-(3-acetoxy-4-methoxy-phenyl)-6-methoxy-chromen-4-one|Tri-Ac-3,5,7-Trihydroxy-4,6-dimethoxyflavone

4,6-Dimethoxy-3,5,7-tri-O-acetyl-flavon|5,7-diacetoxy-2-(3-acetoxy-4-methoxy-phenyl)-6-methoxy-chromen-4-one|Tri-Ac-3,5,7-Trihydroxy-4,6-dimethoxyflavone

C23H20O10 (456.1056)


   

1,4-Diacetoxy-10-methoxy-5,8,11-trimethyl-1H-benzo[5,6][1,4]dioxepino[3,2-e]isobenzofuran-3,7-dion|1,4-diacetoxy-10-methoxy-5,8,11-trimethyl-1H-benzo[5,6][1,4]dioxepino[3,2-e]isobenzofuran-3,7-dione|hypostictic acid-diacetate

1,4-Diacetoxy-10-methoxy-5,8,11-trimethyl-1H-benzo[5,6][1,4]dioxepino[3,2-e]isobenzofuran-3,7-dion|1,4-diacetoxy-10-methoxy-5,8,11-trimethyl-1H-benzo[5,6][1,4]dioxepino[3,2-e]isobenzofuran-3,7-dione|hypostictic acid-diacetate

C23H20O10 (456.1056)


   
   

(-)-Epicatechin-3-(3-O-methylgallate)

(-)-Epicatechin-3-(3-O-methylgallate)

C23H20O10 (456.1056)


   

Riboflavine 5-phosphate

Riboflavine 5-phosphate

C17H21N4O9P (456.1046)


   

Riboflavine phosphate

Riboflavin-5′-monophosphate sodium salt hydrate

C17H21N4O9P (456.1046)


   

Flavin mononucleotide

Flavin mononucleotide

C17H21N4O9P (456.1046)


A flavin mononucleotide that is riboflavin (vitamin B2) in which the primary hydroxy group has been converted to its dihydrogen phosphate ester. D018977 - Micronutrients > D014815 - Vitamins

   

Riboflavin 5-monophosphate_major

Riboflavin 5-monophosphate_major

C17H21N4O9P (456.1046)


   

Cys Cys Met Thr

(2S,3R)-2-[(2S)-2-[(2R)-2-[(2R)-2-amino-3-sulfanylpropanamido]-3-sulfanylpropanamido]-4-(methylsulfanyl)butanamido]-3-hydroxybutanoic acid

C15H28N4O6S3 (456.1171)


   

Cys Cys Thr Met

(2S)-2-[(2S,3R)-2-[(2R)-2-[(2R)-2-amino-3-sulfanylpropanamido]-3-sulfanylpropanamido]-3-hydroxybutanamido]-4-(methylsulfanyl)butanoic acid

C15H28N4O6S3 (456.1171)


   

Cys Met Cys Thr

(2S,3R)-2-[(2R)-2-[(2S)-2-[(2R)-2-amino-3-sulfanylpropanamido]-4-(methylsulfanyl)butanamido]-3-sulfanylpropanamido]-3-hydroxybutanoic acid

C15H28N4O6S3 (456.1171)


   

Cys Met Thr Cys

(2R)-2-[(2S,3R)-2-[(2S)-2-[(2R)-2-amino-3-sulfanylpropanamido]-4-(methylsulfanyl)butanamido]-3-hydroxybutanamido]-3-sulfanylpropanoic acid

C15H28N4O6S3 (456.1171)


   

Cys Thr Cys Met

(2S)-2-[(2R)-2-[(2S,3R)-2-[(2R)-2-amino-3-sulfanylpropanamido]-3-hydroxybutanamido]-3-sulfanylpropanamido]-4-(methylsulfanyl)butanoic acid

C15H28N4O6S3 (456.1171)


   

Cys Thr Met Cys

(2R)-2-[(2S)-2-[(2S,3R)-2-[(2R)-2-amino-3-sulfanylpropanamido]-3-hydroxybutanamido]-4-(methylsulfanyl)butanamido]-3-sulfanylpropanoic acid

C15H28N4O6S3 (456.1171)


   

Met Cys Cys Thr

(2S,3R)-2-[(2R)-2-[(2R)-2-[(2S)-2-amino-4-(methylsulfanyl)butanamido]-3-sulfanylpropanamido]-3-sulfanylpropanamido]-3-hydroxybutanoic acid

C15H28N4O6S3 (456.1171)


   

Met Cys Thr Cys

(2R)-2-[(2S,3R)-2-[(2R)-2-[(2S)-2-amino-4-(methylsulfanyl)butanamido]-3-sulfanylpropanamido]-3-hydroxybutanamido]-3-sulfanylpropanoic acid

C15H28N4O6S3 (456.1171)


   

Met Thr Cys Cys

(2R)-2-[(2R)-2-[(2S,3R)-2-[(2S)-2-amino-4-(methylsulfanyl)butanamido]-3-hydroxybutanamido]-3-sulfanylpropanamido]-3-sulfanylpropanoic acid

C15H28N4O6S3 (456.1171)


   

Thr Cys Cys Met

(2S)-2-[(2R)-2-[(2R)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]-3-sulfanylpropanamido]-3-sulfanylpropanamido]-4-(methylsulfanyl)butanoic acid

C15H28N4O6S3 (456.1171)


   

Thr Cys Met Cys

(2R)-2-[(2S)-2-[(2R)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]-3-sulfanylpropanamido]-4-(methylsulfanyl)butanamido]-3-sulfanylpropanoic acid

C15H28N4O6S3 (456.1171)


   

Thr Met Cys Cys

(2R)-2-[(2R)-2-[(2S)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]-4-(methylsulfanyl)butanamido]-3-sulfanylpropanamido]-3-sulfanylpropanoic acid

C15H28N4O6S3 (456.1171)


   

Epicatechin 3-O-(3-O-methylgallate)

Epicatechin 3-O-(3-O-methylgallate)

C23H20O10 (456.1056)


   

3-O-(4-Methylgalloyl)epicatechin

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,5-dihydroxy-4-methoxybenzoate

C23H20O10 (456.1056)


   

(-)-ecg-3-o-me

epicatechin 3-O-(3-O-methylgallate)

C23H20O10 (456.1056)


A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of epicatechin.

   

Vat Violet 10

Vat Violet 10

C34H16O2 (456.115)


   

Violanthrone

Violanthrone

C34H16O2 (456.115)


   
   

BRAF inhibitor

BRAF inhibitor

C22H18F2N4O3S (456.1068)


BRAF inhibitor is a B-Raf inhibitor extracted from patent WO/2011103196 A1, Compound P-0850.

   
   

2-Deoxy-3,4-Bis-O-[3-(4-Hydroxyphenyl)propanoyl]-L-Threo-Pentaric Acid

2-Deoxy-3,4-Bis-O-[3-(4-Hydroxyphenyl)propanoyl]-L-Threo-Pentaric Acid

C23H20O10 (456.1056)


   

Flavin mononucleotide semiquinone

Flavin mononucleotide semiquinone

C17H21N4O9P (456.1046)


   

Riboflavine 5-(dihydrogen phosphate)

Riboflavine 5-(dihydrogen phosphate)

C17H21N4O9P (456.1046)


   

6-(2-bromo-3,6-dimethoxyphenyl)-9,9-dimethyl-6,8,10,11-tetrahydro-5H-benzo[b][1,4]benzodiazepin-7-one

6-(2-bromo-3,6-dimethoxyphenyl)-9,9-dimethyl-6,8,10,11-tetrahydro-5H-benzo[b][1,4]benzodiazepin-7-one

C23H25BrN2O3 (456.1048)


   
   

4-o-Methylepicatechin-3-o-gallate

4-o-Methylepicatechin-3-o-gallate

C23H20O10 (456.1056)


A natural product found in Parapiptadenia rigida.

   

3,4,5-Trihydroxy-6-[(4,5,6-trihydroxy-2-{[(3-methoxy-3-oxopropanoyl)oxy]methyl}oxan-3-yl)oxy]oxane-2-carboxylic acid

3,4,5-Trihydroxy-6-[(4,5,6-trihydroxy-2-{[(3-methoxy-3-oxopropanoyl)oxy]methyl}oxan-3-yl)oxy]oxane-2-carboxylic acid

C16H24O15 (456.1115)


   

FMNH2(2-)

FMNH2(2-)

C17H21N4O9P (456.1046)


Dianion of reduced flavin mononucleotide arising from deprotonation of both phosphate OH groups.

   
   
   

methyl (1s,4ar,5s,6r,7r,7as)-6-chloro-4a,5,7-trihydroxy-7-methyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate

methyl (1s,4ar,5s,6r,7r,7as)-6-chloro-4a,5,7-trihydroxy-7-methyl-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate

C17H25ClO12 (456.1034)


   

17-chloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

17-chloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

C28H21ClO4 (456.1128)


   

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 3,4-dihydroxy-5-methoxybenzoate

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 3,4-dihydroxy-5-methoxybenzoate

C23H20O10 (456.1056)


   

(20z)-17-chloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

(20z)-17-chloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

C28H21ClO4 (456.1128)


   

methyl 6-chloro-4a,5,7-trihydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate

methyl 6-chloro-4a,5,7-trihydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate

C17H25ClO12 (456.1034)


   

5,7-bis(acetyloxy)-8-methoxy-2-(4-methoxyphenyl)-4-oxochromen-3-yl acetate

5,7-bis(acetyloxy)-8-methoxy-2-(4-methoxyphenyl)-4-oxochromen-3-yl acetate

C23H20O10 (456.1056)


   

(3'r,4's,5'r,8s)-3',4',5-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-9h-spiro[furo[2,3-h]chromene-8,2'-oxolan]-5'-ylmethyl acetate

(3'r,4's,5'r,8s)-3',4',5-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-9h-spiro[furo[2,3-h]chromene-8,2'-oxolan]-5'-ylmethyl acetate

C23H20O10 (456.1056)


   

(2r,3r)-2-(3,4-dihydroxyphenyl)-6,8-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 3,5-dihydroxy-4-methoxybenzoate

(2r,3r)-2-(3,4-dihydroxyphenyl)-6,8-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 3,5-dihydroxy-4-methoxybenzoate

C23H20O10 (456.1056)


   

2-(3,4-dihydroxyphenyl)-6,8-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 3,5-dihydroxy-4-methoxybenzoate

2-(3,4-dihydroxyphenyl)-6,8-dihydroxy-3,4-dihydro-2h-1-benzopyran-3-yl 3,5-dihydroxy-4-methoxybenzoate

C23H20O10 (456.1056)


   

2-hydroxy-1,7-dimethoxy-4,6,11-trioxo-3-propanoyl-4a,12-dihydro-1h-5-oxatetracene-12a-carboxylic acid

2-hydroxy-1,7-dimethoxy-4,6,11-trioxo-3-propanoyl-4a,12-dihydro-1h-5-oxatetracene-12a-carboxylic acid

C23H20O10 (456.1056)


   

(3'r,4's,5'r,8r)-3',4',5-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-9h-spiro[furo[2,3-h]chromene-8,2'-oxolan]-5'-ylmethyl acetate

(3'r,4's,5'r,8r)-3',4',5-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-9h-spiro[furo[2,3-h]chromene-8,2'-oxolan]-5'-ylmethyl acetate

C23H20O10 (456.1056)


   

(3's,4's,5'r,8r)-3',4',5-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-9h-spiro[furo[2,3-h]chromene-8,2'-oxolan]-5'-ylmethyl acetate

(3's,4's,5'r,8r)-3',4',5-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-9h-spiro[furo[2,3-h]chromene-8,2'-oxolan]-5'-ylmethyl acetate

C23H20O10 (456.1056)


   

11-[(3,4-dihydroxy-5-methoxyoxan-2-yl)oxy]-15-hydroxy-6,8,20-trioxapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,4,9,11,14,16,18-heptaen-13-one

11-[(3,4-dihydroxy-5-methoxyoxan-2-yl)oxy]-15-hydroxy-6,8,20-trioxapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,4,9,11,14,16,18-heptaen-13-one

C23H20O10 (456.1056)


   

3',4',5-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-9h-spiro[furo[2,3-h]chromene-8,2'-oxolan]-5'-ylmethyl acetate

3',4',5-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-9h-spiro[furo[2,3-h]chromene-8,2'-oxolan]-5'-ylmethyl acetate

C23H20O10 (456.1056)


   

(3s,7r)-11-{[(2r,3r,4r,5s)-3,4-dihydroxy-5-methoxyoxan-2-yl]oxy}-15-hydroxy-6,8,20-trioxapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,4,9,11,14,16,18-heptaen-13-one

(3s,7r)-11-{[(2r,3r,4r,5s)-3,4-dihydroxy-5-methoxyoxan-2-yl]oxy}-15-hydroxy-6,8,20-trioxapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,4,9,11,14,16,18-heptaen-13-one

C23H20O10 (456.1056)


   

[(2s,3r,4r)-2,3,4-trihydroxy-5-{4-hydroxy-7,8-dimethyl-2-oxobenzo[g]pteridin-10-yl}pentyl]oxyphosphonic acid

[(2s,3r,4r)-2,3,4-trihydroxy-5-{4-hydroxy-7,8-dimethyl-2-oxobenzo[g]pteridin-10-yl}pentyl]oxyphosphonic acid

C17H21N4O9P (456.1046)


   

(2r,3r)-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,4-dihydro-2h-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

(2r,3r)-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,4-dihydro-2h-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C23H20O10 (456.1056)


   

methyl (1r,2s,4s)-2,4,5,7,12-pentahydroxy-6,11-dioxo-2-(2-oxopropyl)-3,4-dihydro-1h-tetracene-1-carboxylate

methyl (1r,2s,4s)-2,4,5,7,12-pentahydroxy-6,11-dioxo-2-(2-oxopropyl)-3,4-dihydro-1h-tetracene-1-carboxylate

C23H20O10 (456.1056)


   

13-(acetyloxy)-5-methoxy-4,7,12-trimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-17-yl acetate

13-(acetyloxy)-5-methoxy-4,7,12-trimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-17-yl acetate

C23H20O10 (456.1056)


   

(20e)-17-chloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

(20e)-17-chloropentacyclo[20.2.2.1¹⁰,¹⁴.1¹⁵,¹⁹.0²,⁷]octacosa-1(25),2,4,6,10,12,14(28),15(27),16,18,20,22(26),23-tridecaene-5,13,16,24-tetrol

C28H21ClO4 (456.1128)


   

(17s)-13-(acetyloxy)-5-methoxy-4,7,12-trimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-17-yl acetate

(17s)-13-(acetyloxy)-5-methoxy-4,7,12-trimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-17-yl acetate

C23H20O10 (456.1056)