Exact Mass: 730.1688884

Exact Mass Matches: 730.1688884

Found 57 metabolites which its exact mass value is equals to given mass value 730.1688884, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

4-Deoxy-4-thio-alpha-D-digitoxosyl-calicheamicin T0

4-Deoxy-4-thio-alpha-D-digitoxosyl-calicheamicin T0

C30H38N2O11S4 (730.1358358)


   

ent-Epicatechin-(4alpha->8)-ent-epicatechin 3'-gallate

2-(3,4-Dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoic acid

C37H30O16 (730.153378)


ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate is found in fruits. ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate is a constituent of Byrsonima crassifolia (nance). Isolated from Thea sinensis (tea). Procyanidin dimer B2 3-gallate is found in tea and common grape.

   

ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate

2-(3,4-Dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoic acid

C37H30O16 (730.153378)


ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate is found in fruits. ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate is a constituent of Byrsonima crassifolia (nance). Constituent of Byrsonima crassifolia (nance). ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate is found in fruits.

   

Epicatechin-(4beta->6)-catechin 3-gallate

(2R,3R,4S)-2-(3,4-Dihydroxyphenyl)-4-[(2R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-6-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoic acid

C37H30O16 (730.153378)


Epicatechin-(4beta->6)-catechin 3-gallate is a member of the class of compounds known as biflavonoids and polyflavonoids. Biflavonoids and polyflavonoids are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3-C3, and C6-C8. Epicatechin-(4beta->6)-catechin 3-gallate is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Epicatechin-(4beta->6)-catechin 3-gallate can be found in common grape, which makes epicatechin-(4beta->6)-catechin 3-gallate a potential biomarker for the consumption of this food product.

   

Procyanidin B2 3-gallate

(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C37H30O16 (730.153378)


Procyanidin b2 3-gallate is a member of the class of compounds known as biflavonoids and polyflavonoids. Biflavonoids and polyflavonoids are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3-C3, and C6-C8. Procyanidin b2 3-gallate is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Procyanidin b2 3-gallate can be synthesized from gallic acid. Procyanidin b2 3-gallate can also be synthesized into procyanidin B2. Procyanidin b2 3-gallate can be found in common grape, which makes procyanidin b2 3-gallate a potential biomarker for the consumption of this food product.

   

Catechin-(4alpha->8)-epicatechin 3'-gallate

(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C37H30O16 (730.153378)


Catechin-(4alpha->8)-epicatechin 3-gallate, also known as (-)-epicatechin-(4a->8)-(+)-catechin-3-O-gallate, is a member of the class of compounds known as biflavonoids and polyflavonoids. Biflavonoids and polyflavonoids are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3-C3, and C6-C8. Catechin-(4alpha->8)-epicatechin 3-gallate is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Catechin-(4alpha->8)-epicatechin 3-gallate can be synthesized from gallic acid. Catechin-(4alpha->8)-epicatechin 3-gallate can also be synthesized into procyanidin B4. Catechin-(4alpha->8)-epicatechin 3-gallate can be found in common grape and tea, which makes catechin-(4alpha->8)-epicatechin 3-gallate a potential biomarker for the consumption of these food products.

   

Epicatechin-(4beta->8)-catechin 3-gallate

(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C37H30O16 (730.153378)


Epicatechin-(4beta->8)-catechin 3-gallate is a member of the class of compounds known as biflavonoids and polyflavonoids. Biflavonoids and polyflavonoids are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3-C3, and C6-C8. Epicatechin-(4beta->8)-catechin 3-gallate is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Epicatechin-(4beta->8)-catechin 3-gallate can be synthesized from gallic acid. Epicatechin-(4beta->8)-catechin 3-gallate can also be synthesized into procyanidin B1. Epicatechin-(4beta->8)-catechin 3-gallate can be found in common grape, which makes epicatechin-(4beta->8)-catechin 3-gallate a potential biomarker for the consumption of this food product.

   

Epicatechin-(4beta->8)-epicatechin 3'-gallate

(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C37H30O16 (730.153378)


Epicatechin-(4beta->8)-epicatechin 3-gallate is a member of the class of compounds known as biflavonoids and polyflavonoids. Biflavonoids and polyflavonoids are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3-C3, and C6-C8. Epicatechin-(4beta->8)-epicatechin 3-gallate is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Epicatechin-(4beta->8)-epicatechin 3-gallate can be synthesized from gallic acid. Epicatechin-(4beta->8)-epicatechin 3-gallate can also be synthesized into procyanidin B2. Epicatechin-(4beta->8)-epicatechin 3-gallate can be found in common buckwheat, common grape, and tea, which makes epicatechin-(4beta->8)-epicatechin 3-gallate a potential biomarker for the consumption of these food products.

   

8)-epicatechin

3-O-Galloylepicatechin-(4beta-

C37H30O16 (730.153378)


   
   

Isorientin 4-O-glucoside 2-O-p-hydroxybenzoate

5,7,3,4-Tetrahydroxyflavone 6-C- (2"-O-p-hydroxybenzoylglucoside) -4-O-glucoside

C34H34O18 (730.1745064)


   

6)-catechin

3-O-Galloylepicatechin-(4beta-

C37H30O16 (730.153378)


   

Procyanidin B5 3-O-gallate

(+)-Procyanidin B5 3-O-gallate

C37H30O16 (730.153378)


   

Gallocatechin-(4alpha-

8)-epigallocatechin-3-O-(4-hydroxybenzoate)

C37H30O16 (730.153378)


   
   

8)-catechin

3-O-Galloylepicatechin-(4beta-

C37H30O16 (730.153378)


   

Catechin-(4alpha-

8)-epicatechin-3-O-gallate

C37H30O16 (730.153378)


   

8)-ent-epicatechin

3-O-Galloyl-ent-epicatechin-(4alpha-

C37H30O16 (730.153378)


   

Epigallocatechin-(4beta-

8)-epigallocatechin 3-O-(4-hydroxybenzoate)

C37H30O16 (730.153378)


   

Epicatechin-(4beta-

8)-epicatechin-3-O-gallate

C37H30O16 (730.153378)


   

Theaflavin 3-(3-O-methylgallate)

Theaflavin 3-(3-O-methylgallate)

C37H30O16 (730.153378)


   

3-O-Galloylepigallocatechin-(4beta->8)-catechin

3-O-Galloylepigallocatechin-(4beta->8)-catechin

C37H30O16 (730.153378)


   

3-(4-O-Hydroxybenzoyl-beta-D-glucopyranoside)-Populnin

3-(4-O-Hydroxybenzoyl-beta-D-glucopyranoside)-Populnin

C34H34O18 (730.1745064)


   

epicatechin-(4beta->8)-epigallocatechin

epicatechin-(4beta->8)-epigallocatechin

C37H30O16 (730.153378)


   

9-(1,3-benzodioxol-5-yl)-4-[(3-O-acetyl-6-deoxy-4-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]-6,7-dimethoxynaphtho[2,3-c]furan-1(3H)-one|justiprocumins A

9-(1,3-benzodioxol-5-yl)-4-[(3-O-acetyl-6-deoxy-4-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)oxy]-6,7-dimethoxynaphtho[2,3-c]furan-1(3H)-one|justiprocumins A

C35H38O17 (730.2108898)


   
   

1,4,6-trihydroxy-8-O-[2-(4-hydroxy-3-methoxy-E-cinnamyl)-beta-D-xylopyranosyl-(1?6)-beta-D-glucopyranosyl]-xanthone|comastomaside E

1,4,6-trihydroxy-8-O-[2-(4-hydroxy-3-methoxy-E-cinnamyl)-beta-D-xylopyranosyl-(1?6)-beta-D-glucopyranosyl]-xanthone|comastomaside E

C34H34O18 (730.1745064)


   

6-hydroxyluteolin 7-O-[6-benzoyl-beta-D-glucopyranosyl-(1->2)]-beta-D-glucopyranoside|aphyllanthoside

6-hydroxyluteolin 7-O-[6-benzoyl-beta-D-glucopyranosyl-(1->2)]-beta-D-glucopyranoside|aphyllanthoside

C34H34O18 (730.1745064)


   

3-O-Galloylepicatechin-(4beta->6)-catechin

3-O-Galloylepicatechin-(4beta->6)-catechin

C37H30O16 (730.153378)


   

epigallocatechin-(4beta->8)-epigallocatechin-3-O-gallate

epigallocatechin-(4beta->8)-epigallocatechin-3-O-gallate

C37H30O16 (730.153378)


   

Epigallocatechin-(4beta->8)-epigallocatechin 3-O-(4-hydroxybenzoate)

Epigallocatechin-(4beta->8)-epigallocatechin 3-O-(4-hydroxybenzoate)

C37H30O16 (730.153378)


   

cyanidin 3-O-glucoside-7-O-(6-O-(p-hydroxybenzoyl)-glucoside)

cyanidin 3-O-glucoside-7-O-(6-O-(p-hydroxybenzoyl)-glucoside)

C34H34O18 (730.1745064)


   

Isorientin 4-O-glucoside 2-O-p-hydroxybenzoagte

Isorientin 4-O-glucoside 2-O-p-hydroxybenzoagte

C34H34O18 (730.1745064)


   

3-Galloylprocyanidin B1

2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C37H30O16 (730.153378)


   

3'-Galloylprocyanidin B2

2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C37H30O16 (730.153378)


   

ent-Epicatechin-(4alpha-

8)-ent-epicatechin-3-O-gallate

C37H30O16 (730.153378)


   

(2R)-5-[[(2S)-2-amino-3-[[(2S)-3-carboxy-1-[[(1R)-1-carboxy-2-sulfanylethyl]amino]-1-oxopropan-2-yl]amino]-3-oxopropyl]amino]-5-oxo-2-[[4-[(4-oxo-3H-pteridin-6-yl)methylamino]benzoyl]amino]pentanoic acid

(2R)-5-[[(2S)-2-amino-3-[[(2S)-3-carboxy-1-[[(1R)-1-carboxy-2-sulfanylethyl]amino]-1-oxopropan-2-yl]amino]-3-oxopropyl]amino]-5-oxo-2-[[4-[(4-oxo-3H-pteridin-6-yl)methylamino]benzoyl]amino]pentanoic acid

C29H34N10O11S (730.2129134)


   

Epicatechin-(4beta->8)-epicatechin 3'-gallate

(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C37H30O16 (730.153378)


Epicatechin-(4beta->8)-epicatechin 3-gallate is a member of the class of compounds known as biflavonoids and polyflavonoids. Biflavonoids and polyflavonoids are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3-C3, and C6-C8. Epicatechin-(4beta->8)-epicatechin 3-gallate is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Epicatechin-(4beta->8)-epicatechin 3-gallate can be synthesized from gallic acid. Epicatechin-(4beta->8)-epicatechin 3-gallate can also be synthesized into procyanidin B2. Epicatechin-(4beta->8)-epicatechin 3-gallate can be found in common buckwheat, common grape, and tea, which makes epicatechin-(4beta->8)-epicatechin 3-gallate a potential biomarker for the consumption of these food products.

   

procyanidin B4 3-O-gallate

procyanidin B4 3-O-gallate

C37H30O16 (730.153378)


A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3S)-hydroxy group of procyanidin B4. A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of procyanidin B4.

   

procyanidin B1 3-O-gallate

procyanidin B1 3-O-gallate

C37H30O16 (730.153378)


A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3S)-hydroxy group of procyanidin B1. A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of procyanidin B1.

   

Epicatechin-(4beta->6)-catechin 3-gallate

Epicatechin-(4beta->6)-catechin 3-gallate

C37H30O16 (730.153378)


   

procyanidin B3 3-O-gallate

procyanidin B3 3-O-gallate

C37H30O16 (730.153378)


A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3S)-hydroxy group of procyanidin B3.

   

(-)-epicatechin-(4alpha->8)-(-)-epicatechin-3-O-gallate

(-)-epicatechin-(4alpha->8)-(-)-epicatechin-3-O-gallate

C37H30O16 (730.153378)


A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of (-)-epicatechin-(4alpha->8)-(-)-epicatechin.

   

GlcA3S(b1-3)Gal(b1-3)Gal(b1-4)Xyl

GlcA3S(b1-3)Gal(b1-3)Gal(b1-4)Xyl

C23H38O24S (730.1473668000001)


   

GlcA3S(b1-3)Gal(b1-3)Gal(b1-4)a-Xyl

GlcA3S(b1-3)Gal(b1-3)Gal(b1-4)a-Xyl

C23H38O24S (730.1473668000001)


   

GlcA(b1-3)Gal4S(b1-3)Gal(b1-4)b-Xyl

GlcA(b1-3)Gal4S(b1-3)Gal(b1-4)b-Xyl

C23H38O24S (730.1473668000001)


   

[6-[2-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxybenzoate

[6-[2-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxybenzoate

C34H34O18 (730.1745064)


   

Procyanidin B2 3-O-gallate

Procyanidin B2 3-O-gallate

C37H30O16 (730.153378)


A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of procyanidin B2.

   

procyanidin B2 3-O-gallate

procyanidin B2 3-O-gallate

C37H30O16 (730.153378)


A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of procyanidin B2.

   

ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate

ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate

C37H30O16 (730.153378)


   
   

2-[5,7-dihydroxy-2-(3-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4-oxochromen-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl 4-hydroxybenzoate

2-[5,7-dihydroxy-2-(3-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4-oxochromen-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl 4-hydroxybenzoate

C34H34O18 (730.1745064)


   

{6-[(2-{[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl)oxy]-3,4,5-trihydroxyoxan-2-yl}methyl benzoate

{6-[(2-{[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl)oxy]-3,4,5-trihydroxyoxan-2-yl}methyl benzoate

C34H34O18 (730.1745064)


   

8-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

8-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C37H30O16 (730.153378)


   

(2r,3r)-8-[(2s,4r)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

(2r,3r)-8-[(2s,4r)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

C37H30O16 (730.153378)