Exact Mass: 536.0434766000001

Exact Mass Matches: 536.0434766000001

Found 48 metabolites which its exact mass value is equals to given mass value 536.0434766000001, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

UDP Xylose

{[(2R,3S,4R)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}({[hydroxy({[(3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy})phosphoryl]oxy})phosphinic acid

C14H22N2O16P2 (536.0444552)


Acquisition and generation of the data is financially supported in part by CREST/JST. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

UDP-D-apiose

[({[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}(hydroxy)phosphoryl)oxy]({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-hydroxy-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy})phosphinic acid

C14H22N2O16P2 (536.0444552)


D-apiose is a plant-specific branched-chain monosaccharide found in rhamnogalacturonan II (RG-II), apiogalacturonan, and several apioglycosides. Within RG-II, d-apiose serves as the binding site for borate, which leads to the formation of cross-links within the wall. Biochemical studies in duckweed and parsley have established that uridine 5-diphospho-d-apiose (UDP-d-apiose) is formed from UDP-d-glucuronate by decarboxylation and re-arrangement of the carbon skeleton, leading to ring contraction and branch formation. The enzyme catalyzing this reaction also forms UDP-d-xylose by decarboxylation of UDP-d-glucuronate, and has therefore been named UDP-d-apiose/UDP-d-xylose synthase. (PMID: 12969423) [HMDB] D-Apiose is a plant-specific branched-chain monosaccharide found in rhamnogalacturonan II (RG-II), apiogalacturonan, and several apioglycosides. Within RG-II, D-apiose serves as the binding site for borate, which leads to the formation of cross-links within the wall. Biochemical studies in duckweed and parsley have established that uridine 5-diphospho-D-apiose (UDP-D-apiose) is formed from UDP-D-glucuronate by decarboxylation and re-arrangement of the carbon skeleton, leading to ring contraction and branch formation. The enzyme catalyzing this reaction also forms UDP-D-xylose by decarboxylation of UDP-D-glucuronate, and has therefore been named UDP-D-apiose/UDP-D-xylose synthase (PMID: 12969423).

   

UDP-L-arabinofuranose

UDP-L-arabinofuranose; UDP-beta-L-arabinofuranose

C14H22N2O16P2 (536.0444552)


   

UDP-L-arabinose

{[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-hydroxy-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}({[hydroxy({[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy})phosphoryl]oxy})phosphinic acid

C14H22N2O16P2 (536.0444552)


UDP-sugars, activated forms of monosaccharides, are synthesized through de novo and salvage pathways and serve as substrates for the synthesis of polysaccharides, glycolipids, and glycoproteins in higher plants. The enzyme catalyzed the formation of UDP-Glc, UDP-Gal, UDP-glucuronic acid, UDP-l-arabinose, and UDP-xylose from respective monosaccharide 1-phosphates in the presence of UTP as a co-substrate, indicating that the enzyme has broad substrate specificity toward monosaccharide 1-phosphates. [HMDB] UDP-sugars, activated forms of monosaccharides, are synthesized through de novo and salvage pathways and serve as substrates for the synthesis of polysaccharides, glycolipids, and glycoproteins in higher plants. The enzyme catalyzed the formation of UDP-Glc, UDP-Gal, UDP-glucuronic acid, UDP-l-arabinose, and UDP-xylose from respective monosaccharide 1-phosphates in the presence of UTP as a co-substrate, indicating that the enzyme has broad substrate specificity toward monosaccharide 1-phosphates.

   

UDP-D-Xylose

[({[(2R,3S,4R,5R)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]({[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy})phosphinic acid

C14H22N2O16P2 (536.0444552)


Uridine diphosphate xylose is important intermediate in the Nucleotide sugars metabolism and chondroitin sulfate biosynthesis (KEGG); The decarboxylation product of UDPglucuronic acid, which is used for formation of the xylosides of seryl hydroxyl groups in mucoprotein synthesis.; Uridine is a molecule (known as a nucleoside) that is formed when uracil is attached to a ribose ring (also known as a ribofuranose) via a ?-N1-glycosidic bond. Udp-xylose is found in soy bean. Uridine diphosphate xylose is important intermediate in the Nucleotide sugars metabolism and chondroitin sulfate biosynthesis (KEGG). The decarboxylation product of UDPglucuronic acid, which is used for formation of the xylosides of seryl hydroxyl groups in mucoprotein synthesis. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

3,3',5,5'-Tetrahydroxy-6,7-methyleneoxy-4'-methoxyflavone 3-glucuronide

6-{[6-(3,5-dihydroxy-4-methoxyphenyl)-9-hydroxy-8-oxo-2H,8H-[1,3]dioxolo[4,5-g]chromen-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

C23H20O15 (536.0802170000001)


3,3,5,5-Tetrahydroxy-6,7-methyleneoxy-4-methoxyflavone 3-glucuronide is found in green vegetables. 3,3,5,5-Tetrahydroxy-6,7-methyleneoxy-4-methoxyflavone 3-glucuronide is a constituent of Spinacia oleracea (spinach). Constituent of Spinacia oleracea (spinach). 3,3,5,5-Tetrahydroxy-6,7-methyleneoxy-4-methoxyflavone 3-glucuronide is found in green vegetables and spinach.

   
   

5,2,3-trihydroxy-4-methoxy-6,7-methylenedioxyflavonol 3-O-beta-glucuronide

5,2,3-trihydroxy-4-methoxy-6,7-methylenedioxyflavonol 3-O-beta-glucuronide

C23H20O15 (536.0802170000001)


   

3-Chlorobiphenyl-2,2,4,4,6,6-hexol hexaacetate

3-Chlorobiphenyl-2,2,4,4,6,6-hexol hexaacetate

C24H21ClO12 (536.0721496000001)


   

1,3,4,6,8,15-Hexahydroxy-10-methyl-7,16-dioxodibenzo[a,o]perylene-13-carboxylic acid

1,3,4,6,8,15-Hexahydroxy-10-methyl-7,16-dioxodibenzo[a,o]perylene-13-carboxylic acid

C30H16O10 (536.0743436)


   
   

3,3',5,5'-Tetrahydroxy-6,7-methyleneoxy-4'-methoxyflavone 3-glucuronide

6-{[6-(3,5-dihydroxy-4-methoxyphenyl)-9-hydroxy-8-oxo-2H,8H-[1,3]dioxolo[4,5-g]chromen-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

C23H20O15 (536.0802170000001)


   

buffer solution

1,10-Phenanthrolinedisulfonic acid, 4,7-diphenyl-, disodium salt

C24H14N2Na2O6S2 (536.0088664)


   
   

bathophenanthrolinedisulfonic acid disodium salt trihydrate

bathophenanthrolinedisulfonic acid disodium salt trihydrate

C24H14N2Na2O6S2 (536.0088664)


   

5-Bromo-4-chloro-3-indolyl-a-D-N-acetylneuraminic acid

5-Bromo-4-chloro-3-indolyl-a-D-N-acetylneuraminic acid

C19H22BrClN2O9 (536.0197132000001)


   

calcium,1,4-bis(ethenyl)benzene,4-ethenylbenzenesulfonate

calcium,1,4-bis(ethenyl)benzene,4-ethenylbenzenesulfonate

C26H24CaO6S2 (536.0640154)


   

sodium 4-anilino-6-[(5-chloro-2-hydroxy-3-nitrophenyl)azo]-5-hydroxynaphthalene-1-sulphonate

sodium 4-anilino-6-[(5-chloro-2-hydroxy-3-nitrophenyl)azo]-5-hydroxynaphthalene-1-sulphonate

C22H14ClN4NaO7S (536.0169404000001)


   
   

chlorogold,tris(4-methylphenyl)phosphane

chlorogold,tris(4-methylphenyl)phosphane

C21H21AuClP (536.0734926)


   

Chloro[tri(o-tolyl)phosphine]gold(I)

Chloro[tri(o-tolyl)phosphine]gold(I)

C21H21AuClP (536.0734926)


   
   

N-Sulfo-flavin mononucleotide

N-Sulfo-flavin mononucleotide

C17H21N4O12PS (536.0614276)


   

[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl] [[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate

[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl] [[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate

C14H22N2O16P2 (536.0444552)


   
   
   

[(2r,3s,4r,5r)-5-(2,4-Dioxo-3,4-Dihydropyrimidin-1(2h)-Yl)-3,4-Dihydroxytetrahydrofuran-2-Yl]methyl (2s,3r,4s,5s)-3,4,5-Trihydroxytetrahydro-2h-Pyran-2-Yl Dihydrogen Diphosphate

[(2r,3s,4r,5r)-5-(2,4-Dioxo-3,4-Dihydropyrimidin-1(2h)-Yl)-3,4-Dihydroxytetrahydrofuran-2-Yl]methyl (2s,3r,4s,5s)-3,4,5-Trihydroxytetrahydro-2h-Pyran-2-Yl Dihydrogen Diphosphate

C14H22N2O16P2 (536.0444552)


   

{[(2R,3S,4R)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}({[hydroxy({[(3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy})phosphoryl]oxy})phosphinic acid

{[(2R,3S,4R)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}({[hydroxy({[(3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy})phosphoryl]oxy})phosphinic acid

C14H22N2O16P2 (536.0444552)


   

[(3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate

[(3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate

C14H22N2O16P2 (536.0444552)


   

(10R)-6-carboxy-10-[(9R)-2-carboxy-4-hydroxy-5-oxido-10-oxo-9H-anthracen-9-yl]-8-hydroxy-9-oxo-10H-anthracen-1-olate

(10R)-6-carboxy-10-[(9R)-2-carboxy-4-hydroxy-5-oxido-10-oxo-9H-anthracen-9-yl]-8-hydroxy-9-oxo-10H-anthracen-1-olate

C30H16O10-2 (536.0743436)


   

Uridine 5-diphosphoric acid beta-alpha-L-arabinofuranosyl ester

Uridine 5-diphosphoric acid beta-alpha-L-arabinofuranosyl ester

C14H22N2O16P2 (536.0444552)


   

(10S)-6-carboxy-10-[(9R)-2-carboxy-4-hydroxy-5-oxido-10-oxo-9H-anthracen-9-yl]-8-hydroxy-9-oxo-10H-anthracen-1-olate

(10S)-6-carboxy-10-[(9R)-2-carboxy-4-hydroxy-5-oxido-10-oxo-9H-anthracen-9-yl]-8-hydroxy-9-oxo-10H-anthracen-1-olate

C30H16O10-2 (536.0743436)


   

[(3S)-3-acetamido-4-[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-4-oxobutyl]-oxido-oxophosphanium

[(3S)-3-acetamido-4-[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-4-oxobutyl]-oxido-oxophosphanium

C16H22N6O11P2 (536.0821762)


   
   

[4-(Benzenesulfonyl)-1-piperazinyl]-[6-bromo-2-(2-pyridinyl)-4-quinolinyl]methanone

[4-(Benzenesulfonyl)-1-piperazinyl]-[6-bromo-2-(2-pyridinyl)-4-quinolinyl]methanone

C25H21BrN4O3S (536.0517656000001)


   
   

[(3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate

[(3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate

C14H22N2O16P2 (536.0444552)


   

[[(2S,3R,4S,5S)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl] hydrogen phosphate

[[(2S,3R,4S,5S)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl] hydrogen phosphate

C14H22N2O16P2 (536.0444552)


   
   

UDP-alpha-D-xylose

UDP-alpha-D-xylose

C14H22N2O16P2 (536.0444552)


A UDP-sugar having alpha-xylose as the sugar component. It is an important metabolite in the nucleotide sugar metabolism in animals, plants, fungi, and bacteria.

   
   

3,3,5,5-Tetrahydroxy-6,7-methyleneoxy-4-methoxyflavone 3-glucuronide

3,3,5,5-Tetrahydroxy-6,7-methyleneoxy-4-methoxyflavone 3-glucuronide

C23H20O15 (536.0802170000001)


   

Cladofulvin(2-)

Cladofulvin(2-)

C30H16O10 (536.0743436)


A phenolate anion that is the dianion of cladofulvin, obtained from the deprotonation of the 6 and 7-hydroxy groups. Major species at pH 7.3.

   

(2s,3s,4s,5r,6s)-6-{[6-(2,3-dihydroxy-4-methoxyphenyl)-9-hydroxy-8-oxo-2h-[1,3]dioxolo[4,5-g]chromen-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

(2s,3s,4s,5r,6s)-6-{[6-(2,3-dihydroxy-4-methoxyphenyl)-9-hydroxy-8-oxo-2h-[1,3]dioxolo[4,5-g]chromen-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

C23H20O15 (536.0802170000001)


   

2',4,4',6,6'-pentakis(acetyloxy)-3'-chloro-[1,1'-biphenyl]-2-yl acetate

2',4,4',6,6'-pentakis(acetyloxy)-3'-chloro-[1,1'-biphenyl]-2-yl acetate

C24H21ClO12 (536.0721496000001)


   

6-{[6-(2,3-dihydroxy-4-methoxyphenyl)-9-hydroxy-8-oxo-2h-[1,3]dioxolo[4,5-g]chromen-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

6-{[6-(2,3-dihydroxy-4-methoxyphenyl)-9-hydroxy-8-oxo-2h-[1,3]dioxolo[4,5-g]chromen-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

C23H20O15 (536.0802170000001)


   

{[(2r,3s,4r,5r)-3,4-dihydroxy-5-(4-hydroxy-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy([(2r,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy)phosphinic acid

{[(2r,3s,4r,5r)-3,4-dihydroxy-5-(4-hydroxy-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy([(2r,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy)phosphinic acid

C14H22N2O16P2 (536.0444552)