Exact Mass: 973.1423588000001

Exact Mass Matches: 973.1423588000001

Found 13 metabolites which its exact mass value is equals to given mass value 973.1423588000001, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Sinapoyl-CoA

3-phosphoadenosine 5-{3-[(3R)-3-hydroxy-4-({3-[(2-{[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)amino]-3-oxopropyl}amino)-2,2-dimethyl-4-oxobutyl] dihydrogen diphosphate}

C32H46N7O20P3S (973.1731106000001)


The S-sinapoyl derivative of coenzyme A.

   

2-Carboxymethyl-3-hydroxyphenylpropionyl-CoA

3-[({2-[(3-{[4-({[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-1,2-dihydroxy-3,3-dimethylbutylidene]amino}-1-hydroxypropylidene)amino]ethyl}sulphanyl)carbonyl]-4-hydroxy-4-phenylbutanoic acid

C32H46N7O20P3S (973.1731106000001)


2-Carboxymethyl-3-hydroxyphenylpropionyl-CoA is an intermediate in toluene degradation to benzoyl-CoA. It is a substrate for putative 3-hydroxyacyl-CoA dehydrogenase and can be generated from the hydrolysis of E-phenylitaconyl-CoA. Biodegradation of aromatic compounds is a common process in anoxic environments. The many natural and synthetic aromatic compounds found in the environment are usually degraded by anaerobic microorganisms into only few central intermediates, prior to ring cleavage. Benzoyl-CoA is the most important of these intermediates since a large number of compounds, including chloro-, nitro-, and aminobenzoates, aromatic hydrocarbons, and phenolic compounds, are initially converted to benzoyl-CoA prior to ring reduction and cleavage. [HMDB] 2-Carboxymethyl-3-hydroxyphenylpropionyl-CoA is an intermediate in toluene degradation to benzoyl-CoA. It is a substrate for putative 3-hydroxyacyl-CoA dehydrogenase and can be generated from the hydrolysis of E-phenylitaconyl-CoA. Biodegradation of aromatic compounds is a common process in anoxic environments. The many natural and synthetic aromatic compounds found in the environment are usually degraded by anaerobic microorganisms into only few central intermediates, prior to ring cleavage. Benzoyl-CoA is the most important of these intermediates since a large number of compounds, including chloro-, nitro-, and aminobenzoates, aromatic hydrocarbons, and phenolic compounds, are initially converted to benzoyl-CoA prior to ring reduction and cleavage.

   

3-O-[3-O-(5-Guanylyl)-5-guanylyl]guanosine

3-O-[3-O-(5-Guanylyl)-5-guanylyl]guanosine

C30H37N15O19P2 (973.1865312000001)


   

(4S)-3-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanylcarbonyl]-4-hydroxy-4-phenylbutanoic acid

(4S)-3-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanylcarbonyl]-4-hydroxy-4-phenylbutanoic acid

C32H46N7O20P3S (973.1731106000001)


   
   

[hydroxy(phenyl)methyl]succinyl-CoA

[hydroxy(phenyl)methyl]succinyl-CoA

C32H46N7O20P3S (973.1731106000001)


A hydroxyacyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of [hydroxy(phenyl)methyl]succinic acid.

   

alpha-D-GlcNS-(1->4)-beta-D-GlcA-(1->4)-alpha-D-GlcNS-(1->4)-beta-D-GlcA-O-pNP

alpha-D-GlcNS-(1->4)-beta-D-GlcA-(1->4)-alpha-D-GlcNS-(1->4)-beta-D-GlcA-O-pNP

C30H43N3O29S2 (973.1423588000001)


   

(R,S)-[hydroxy(phenyl)methyl]succinyl-CoA

(R,S)-[hydroxy(phenyl)methyl]succinyl-CoA

C32H46N7O20P3S (973.1731106000001)


   

L-[(N-Hydroxyamino)Carbonyl]Phenylalanine-CoA; (Acyl-CoA); [M+H]+

L-[(N-Hydroxyamino)Carbonyl]Phenylalanine-CoA; (Acyl-CoA); [M+H]+

C31H46N9O19P3S (973.1843436)


   

2-Carboxymethyl-3-hydroxyphenylpropionyl-CoA

2-Carboxymethyl-3-hydroxyphenylpropionyl-CoA

C32H46N7O20P3S (973.1731106000001)


   

(2r)-4-[({[(2s,3r,4s,5r)-5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-2-hydroxy-n-{2-[(2-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)-c-hydroxycarbonimidoyl]ethyl}-3,3-dimethylbutanimidic acid

(2r)-4-[({[(2s,3r,4s,5r)-5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-2-hydroxy-n-{2-[(2-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)-c-hydroxycarbonimidoyl]ethyl}-3,3-dimethylbutanimidic acid

C32H46N7O20P3S (973.1731106000001)


   

(2r)-4-[({[(2r,3s,4r,5r)-5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-2-hydroxy-n-{2-[(2-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)-c-hydroxycarbonimidoyl]ethyl}-3,3-dimethylbutanimidic acid

(2r)-4-[({[(2r,3s,4r,5r)-5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-2-hydroxy-n-{2-[(2-{[(2e)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)-c-hydroxycarbonimidoyl]ethyl}-3,3-dimethylbutanimidic acid

C32H46N7O20P3S (973.1731106000001)