Exact Mass: 418.0820102

Exact Mass Matches: 418.0820102

Found 93 metabolites which its exact mass value is equals to given mass value 418.0820102, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Kaempferol 3-O-arabinoside

3-{[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C20H18O10 (418.0899928)


   

5-Butyrylphosphoinosine

5-Butyrylphosphoinosine; Inosine 5-phosphobutyrate

C14H19N4O9P (418.0889614)


   

Kaempferol 3-O-arabinoside

2-(4-Hydroxyphenyl)-3-[[(2R)-3alpha,4beta-dihydroxy-5alpha-(hydroxymethyl)tetrahydrofuran]-2alpha-yloxy]-5,7-dihydroxy-4H-1-benzopyran-4-one

C20H18O10 (418.0899928)


Kaempferol 3-O-arabinoside is a polyphenol compound found in foods of plant origin (PMID: 20428313) Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1]. Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1].

   

Scutellarein 6-xyloside

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]-4H-chromen-4-one

C20H18O10 (418.0899928)


Scutellarein 6-xyloside is found in fruits. Scutellarein 6-xyloside is isolated from Juniperus communis (juniper). Isolated from Juniperus communis (juniper). Scutellarein 6-xyloside is found in fruits.

   

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-(3,4,5-trihydroxyoxan-2-yl)-4H-chromen-4-one

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-(3,4,5-trihydroxyoxan-2-yl)-4H-chromen-4-one

C20H18O10 (418.0899928)


   

Salvianolic acid G

2-{[(2E)-3-[2-(carboxymethyl)-3,4-dihydroxyphenyl]prop-2-enoyl]oxy}-3-(3,4-dihydroxyphenyl)propanoic acid

C20H18O10 (418.0899928)


Salvianolic acid G is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

Kaempferol 3-alpha-L-arabinofuranoside

3-[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C20H18O10 (418.0899928)


Kaempferol 3-alpha-L-arabinofuranoside is found in common walnut. Kaempferol 3-alpha-L-arabinofuranoside is from leaves of English walnut (Juglans regia From leaves of English walnut (Juglans regia). Kaempferol 3-arabinoside is found in many foods, some of which are jute, pear, nuts, and common walnut. Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1]. Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1].

   

Bifendate

Methyl 7-methoxy-4-[7-methoxy-5-(methoxycarbonyl)-2H-1,3-benzodioxol-4-yl]-2H-1,3-benzodioxole-5-carboxylic acid

C20H18O10 (418.0899928)


   

Epidepride

N-[(1-ethylpyrrolidin-2-yl)methyl]-5-iodo-2,3-dimethoxybenzamide

C16H23IN2O3 (418.07533579999995)


   

2-Benzyl-5-(4-chlorophenyl)-6-(4-methylsulfanylphenyl)pyridazin-3-one

2-Benzyl-5-(4-chlorophenyl)-6-[4-(methylsulphanyl)phenyl]-2,3-dihydropyridazin-3-one

C24H19ClN2OS (418.09065540000006)


   

Kaempferol 3-alpha-D-arabinopyranoside

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-4H-chromen-4-one

C20H18O10 (418.0899928)


Kaempferol 3-alpha-d-arabinopyranoside is a member of the class of compounds known as flavonoid-3-o-glycosides. Flavonoid-3-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. Kaempferol 3-alpha-d-arabinopyranoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Kaempferol 3-alpha-d-arabinopyranoside can be found in avocado, which makes kaempferol 3-alpha-d-arabinopyranoside a potential biomarker for the consumption of this food product.

   

Kaempferol 3-O-beta-D-xylofuranoside

3-{[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C20H18O10 (418.0899928)


Kaempferol 3-o-beta-d-xylofuranoside is also known as kaempferol-3-O-alpha-L-arabinofuranoside. Kaempferol 3-o-beta-d-xylofuranoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Kaempferol 3-o-beta-d-xylofuranoside can be found in horseradish, which makes kaempferol 3-o-beta-d-xylofuranoside a potential biomarker for the consumption of this food product.

   

Juglanin

3-{[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C20H18O10 (418.0899928)


Isolated from walnuts (Juglans regia). Juglanin is found in many foods, some of which are nuts, common hazelnut, fennel, and sweet bay. Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1]. Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1].

   

Kaempferol 7-arabinoside

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxyoxan-2-yl)oxy]-4H-chromen-4-one

C20H18O10 (418.0899928)


Kaempferol 7-arabinoside is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Kaempferol 7-arabinoside is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Kaempferol 7-arabinoside can be found in ostrich fern and radish, which makes kaempferol 7-arabinoside a potential biomarker for the consumption of these food products.

   

Luteolin 7-xyloside

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(3,4,5-trihydroxyoxan-2-yl)oxy]-4H-chromen-4-one

C20H18O10 (418.0899928)


Luteolin 7-xyloside is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Luteolin 7-xyloside is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Luteolin 7-xyloside can be found in anise, which makes luteolin 7-xyloside a potential biomarker for the consumption of this food product.

   

SalvianolicacidD

BENZENEPROPANOIC ACID, .ALPHA.-(((2E)-3-(2-(CARBOXYMETHYL)-3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPEN-1-YL)OXY)-3,4-DIHYDROXY-, (.ALPHA.R)-

C20H18O10 (418.0899928)


Salvianolic acid D is a hydroxycinnamic acid. Salvianolic acid D is a natural product found in Salvia miltiorrhiza and Salvia chinensis with data available.

   

Juglalin

5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-(((2S,3R,4S,5S)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C20H18O10 (418.0899928)


Kaempferol 3-O-arabinoside is a member of flavonoids and a glycoside. Kaempferol 3-O-arabinoside is a natural product found in Xylopia emarginata, Asplenium viride, and other organisms with data available. Acquisition and generation of the data is financially supported in part by CREST/JST.

   

Luteolin 7-xyloside

Luteolin 7-xyloside

C20H18O10 (418.0899928)


   

6-C-Xylosylluteolin

2- (3,4-Dihydroxyphenyl) -5,7-dihydroxy-6-beta-D-xylopyranosyl-4H-1-benzopyran-4-one

C20H18O10 (418.0899928)


   

Luteolin 3-xyloside

3- (beta-D-Xylopyranosyloxy) -4,5,7-trihydroxyflavone

C20H18O10 (418.0899928)


   

Isoscutellarein 7-xyloside

2- (4-Hydroxyphenyl) -5,8-dihydroxy-7- (beta-D-xylopyranosyloxy) -4H-1-benzopyran-4-one

C20H18O10 (418.0899928)


   

Cimicifugic acid D

(+)-Cimicifugic acid D

C20H18O10 (418.0899928)


   

Kaempferol 7-alpha-L-arabinoside

3,5,7,4-Tetrahydroxyflavone 7-alpha-L-arabinoside

C20H18O10 (418.0899928)


   

8-C-alpha-L-arabinosylluteolin

5,7,3,4-Tetrahydroxyflavone 8-C-alpha-L-arabinoside

C20H18O10 (418.0899928)


   
   

Kaempferol 3-alpha-D-arabinopyranoside

3-(alpha-D-Arabinopyranosyloxy)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

C20H18O10 (418.0899928)


   

6-C-alpha-L-Arabinosylluteolin

6-alpha-L-Arabinopyranosyl-2- (3,4-dihydroxyphenyl) -5,7-dihydroxy-4H-1-benzopyran-4-one

C20H18O10 (418.0899928)


   

5,3-Dihydroxy-3,8,4,5-tetramethoxy-6,7-methylenedioxyflavone

5,3-Dihydroxy-3,8,4,5-tetramethoxy-6,7-methylenedioxyflavone

C20H18O10 (418.0899928)


   

Kaempferol 3-xyloside

Kaempferol 3-xyloside

C20H18O10 (418.0899928)


   

Kaempferol 7-xyloside

Kaempferol 7-xyloside

C20H18O10 (418.0899928)


   

Juglanin

3-(((2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)oxy)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C20H18O10 (418.0899928)


Kaempferol 3-arabinofuranoside is a member of flavonoids and a glycoside. Juglanin is a natural product found in Saxifraga tricuspidata, Hedyotis herbacea, and other organisms with data available. Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1]. Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1].

   

Cyanidin 3-o-alpha-L-arabinopyranoside

Cyanidin 3-o-alpha-L-arabinopyranoside

C20H18O10 (418.0899928)


   
   

4-O-alpha-L-Arabinopyranoside-4,5,6,7-Tetrahydroxyflavone

4-O-alpha-L-Arabinopyranoside-4,5,6,7-Tetrahydroxyflavone

C20H18O10 (418.0899928)


   

scutellarein-7-O-beta-D-apiofuranoside

scutellarein-7-O-beta-D-apiofuranoside

C20H18O10 (418.0899928)


   
   

kaempferol-5-O-arabinoside

kaempferol-5-O-arabinoside

C20H18O10 (418.0899928)


   

3-O-beta-D-xylosyltricetin

3-O-beta-D-xylosyltricetin

C20H18O10 (418.0899928)


   

2,3,5,6-Tetra-Ac-2,3,4,5,6-Pentahydroxydiphenyl ether

2,3,5,6-Tetra-Ac-2,3,4,5,6-Pentahydroxydiphenyl ether

C20H18O10 (418.0899928)


   

Luteolin 6-C-alpha-L-arabinopyranoside

Luteolin 6-C-alpha-L-arabinopyranoside

C20H18O10 (418.0899928)


   

1-glucosyloxy-2,3-methylenedioxyxanthone

1-glucosyloxy-2,3-methylenedioxyxanthone

C20H18O10 (418.0899928)


   
   

1-O-<5-deoxy-5-(dimethylarsinoyl)-beta-D-ribosyl>mannitol|1-O-[5-deoxy-5-(dimethylarsinoyl)-beta-D-ribosyl]mannitol

1-O-<5-deoxy-5-(dimethylarsinoyl)-beta-D-ribosyl>mannitol|1-O-[5-deoxy-5-(dimethylarsinoyl)-beta-D-ribosyl]mannitol

C13H27AsO10 (418.0820102)


   

Bifendate

7-methoxy-4-(7-methoxy-5-methoxycarbonyl-1,3-benzodioxol-4-yl)-1,3-benzodioxole-5-carboxylic acid methyl ester

C20H18O10 (418.0899928)


D004791 - Enzyme Inhibitors > D065607 - Cytochrome P-450 Enzyme Inhibitors D007155 - Immunologic Factors

   

CAY10602

1-(4-fluorophenyl)-3-(phenylsulfonyl)-1H-pyrrolo[2,3-b]quinoxalin-2-amine

C22H15FN4O2S (418.0899702)


CAY10602 is a SIRT1 activator. CAY10602 dose-dependently suppresses the NF-κB-dependent induction of TNF-α by lipopolysaccharide in THP-1 cells[1].

   

3-[(2R,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

NCGC00384764-01!3-[(2R,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C20H18O10 (418.0899928)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one

NCGC00180756-02!5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one

C20H18O10 (418.0899928)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one

NCGC00384802-01!5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one

C20H18O10 (418.0899928)


   

kaempferol-3-O-pentoside

kaempferol-3-O-pentoside

C20H18O10 (418.0899928)


   

Kaempferol 3-alpha-L-arabinopyranoside

Kaempferol 3-alpha-L-arabinopyranoside

C20H18O10 (418.0899928)


   

Kaempferol-3-O-arabinoside

Kaempferol-3-O-arabinoside

C20H18O10 (418.0899928)


Annotation level-1

   

Scutellarein 6-xyloside

Scutellarein 6-xyloside

C20H18O10 (418.0899928)


   

Euglanin

3-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C20H18O10 (418.0899928)


Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1]. Juglanin, a natural occurring flavonoid, is a JNK acticator, with inflammation and anti-tumor activities. Juglanin can induce apoptosis and autophagy on human breast cancer cells[1].

   

Salvianolic acid G

2-{[(2E)-3-[2-(carboxymethyl)-3,4-dihydroxyphenyl]prop-2-enoyl]oxy}-3-(3,4-dihydroxyphenyl)propanoic acid

C20H18O10 (418.0899928)


   

(ethylcyclopentadienyl)(triphenylphosphine) copper(i)

(ethylcyclopentadienyl)(triphenylphosphine) copper(i)

C25H24CuP (418.0911524)


   

5-FLUORO-3-IODO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE

5-FLUORO-3-IODO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE

C16H24FIN2Si (418.07374659999994)


   

Di-p-anisoyl-L-tartaric acid

Di-p-anisoyl-L-tartaric acid

C20H18O10 (418.0899928)


   

5-FLUORO-4-IODO-1-(TRIISOPROPYLSILYL)-1H-PYRROLO[2,3-B]PYRIDINE

5-FLUORO-4-IODO-1-(TRIISOPROPYLSILYL)-1H-PYRROLO[2,3-B]PYRIDINE

C16H24FIN2Si (418.07374659999994)


   
   

N-{2-[(1S)-1-(3,4-Dihydroxyphenyl)-2-(methylsulfonyl)ethyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}acetamide

N-{2-[(1S)-1-(3,4-Dihydroxyphenyl)-2-(methylsulfonyl)ethyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}acetamide

C19H18N2O7S (418.08346780000005)


   

Di-p-anisoyl-D-tartaric acid

Di-p-anisoyl-D-tartaric acid

C20H18O10 (418.0899928)


   

4-[(5-Naphthalen-1-yl-1,3,4-oxadiazol-2-yl)sulfanyl]but-2-ynyl 4-fluorobenzoate

4-[(5-Naphthalen-1-yl-1,3,4-oxadiazol-2-yl)sulfanyl]but-2-ynyl 4-fluorobenzoate

C23H15FN2O3S (418.0787372)


   

N-(6-ethoxy-1,3-benzothiazol-2-yl)-1,3-dimethyl-2-oxo-5-benzimidazolesulfonamide

N-(6-ethoxy-1,3-benzothiazol-2-yl)-1,3-dimethyl-2-oxo-5-benzimidazolesulfonamide

C18H18N4O4S2 (418.07694280000004)


   

5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one

5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one

C20H18O10 (418.0899928)


   

Fumiformamide

Fumiformamide

C19H18N2O7S (418.08346780000005)


A natural product found in Aspergillus fumigatus and Streptomyces peucetius.

   

3-Fluorobenzoic acid 4-[[5-(1-naphthalenyl)-1,3,4-oxadiazol-2-yl]thio]but-2-ynyl ester

3-Fluorobenzoic acid 4-[[5-(1-naphthalenyl)-1,3,4-oxadiazol-2-yl]thio]but-2-ynyl ester

C23H15FN2O3S (418.0787372)


   

4-(dimethylsulfamoyl)benzoic acid [2-oxo-2-(3-oxo-4H-1,4-benzoxazin-6-yl)ethyl] ester

4-(dimethylsulfamoyl)benzoic acid [2-oxo-2-(3-oxo-4H-1,4-benzoxazin-6-yl)ethyl] ester

C19H18N2O7S (418.08346780000005)


   

2-Fluorobenzoic acid 4-[[5-(1-naphthalenyl)-1,3,4-oxadiazol-2-yl]thio]but-2-ynyl ester

2-Fluorobenzoic acid 4-[[5-(1-naphthalenyl)-1,3,4-oxadiazol-2-yl]thio]but-2-ynyl ester

C23H15FN2O3S (418.0787372)


   

3-Tert-butyl-7-[2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl]sulfanyl-[1,3,4]thiadiazolo[2,3-c][1,2,4]triazin-4-one

3-Tert-butyl-7-[2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl]sulfanyl-[1,3,4]thiadiazolo[2,3-c][1,2,4]triazin-4-one

C18H18N4O4S2 (418.07694280000004)


   

[2-Acetyloxy-3-[hydroxy-(2,3,4,5,6-pentahydroxycyclohexyl)oxyphosphoryl]oxypropyl] acetate

[2-Acetyloxy-3-[hydroxy-(2,3,4,5,6-pentahydroxycyclohexyl)oxyphosphoryl]oxypropyl] acetate

C13H23O13P (418.0876238)


   

3-[(2R,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

3-[(2R,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C20H18O10 (418.0899928)


   

kaempferol 3-O-beta-D-xyloside

kaempferol 3-O-beta-D-xyloside

C20H18O10 (418.0899928)


A glycosyloxyflavone that is apigenin substituted kaempferol in which the hydroxyl hydrogen at position 3 is replaced by a beta-D-xylosyl residue

   

3-[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

3-[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C20H18O10 (418.0899928)


   
   

n-{3-[(2r,5e)-5-[(6-bromo-1h-indol-3-yl)methylidene]-3,6-dihydroxy-2h-pyrazin-2-yl]propyl}guanidine

n-{3-[(2r,5e)-5-[(6-bromo-1h-indol-3-yl)methylidene]-3,6-dihydroxy-2h-pyrazin-2-yl]propyl}guanidine

C17H19BrN6O2 (418.07527739999995)


   

5-hydroxy-8-[(2r,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]-2-(3,4,5-trihydroxyphenyl)chromen-4-one

5-hydroxy-8-[(2r,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]-2-(3,4,5-trihydroxyphenyl)chromen-4-one

C20H18O10 (418.0899928)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]chromen-4-one

C20H18O10 (418.0899928)


   

5,7-dihydroxy-2-(4-hydroxy-3-oxidophenyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]-1λ⁴-chromen-1-ylium

5,7-dihydroxy-2-(4-hydroxy-3-oxidophenyl)-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]-1λ⁴-chromen-1-ylium

C20H18O10 (418.0899928)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3s,4r,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3s,4r,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}chromen-4-one

C20H18O10 (418.0899928)


   

(2r,3r,4r,5r)-6-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}hexane-1,2,3,4,5-pentol

(2r,3r,4r,5r)-6-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}hexane-1,2,3,4,5-pentol

C13H27AsO10 (418.0820102)


   

5,7-dihydroxy-2-{4-hydroxy-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]phenyl}chromen-4-one

5,7-dihydroxy-2-{4-hydroxy-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]phenyl}chromen-4-one

C20H18O10 (418.0899928)


   

7-[(acetyloxy)methyl]-6,14-dihydroxy-15-(hydroxymethyl)-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaene-5-carboxylic acid

7-[(acetyloxy)methyl]-6,14-dihydroxy-15-(hydroxymethyl)-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaene-5-carboxylic acid

C20H18O10 (418.0899928)


   

7-{[(2s,3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one

7-{[(2s,3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one

C20H18O10 (418.0899928)


   

(2r,3s)-2-[(3,4-dihydroxyphenyl)methyl]-2-hydroxy-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}butanedioic acid

(2r,3s)-2-[(3,4-dihydroxyphenyl)methyl]-2-hydroxy-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}butanedioic acid

C20H18O10 (418.0899928)


   

3-{[(3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxy-3-oxidophenyl)-1λ⁴-chromen-1-ylium

3-{[(3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxy-3-oxidophenyl)-1λ⁴-chromen-1-ylium

C20H18O10 (418.0899928)


   

5,8-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxyoxan-2-yl)oxy]chromen-4-one

5,8-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxyoxan-2-yl)oxy]chromen-4-one

C20H18O10 (418.0899928)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}chromen-4-one

C20H18O10 (418.0899928)