Chemical Formula: C32H46N7O20P3S

Sinapoyl-CoA

C32H46N7O20P3S (973.1731106000001)

The S-sinapoyl derivative of coenzyme A.

2-Carboxymethyl-3-hydroxyphenylpropionyl-CoA

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.

(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)

Sinapoyl-coenzyme A; (Acyl-CoA); [M+H]+

C32H46N7O20P3S (973.1731106000001)

[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.

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

C32H46N7O20P3S (973.1731106000001)

Sinapyl-Coenzyme A

C32H46N7O20P3S (973.1731106000001)

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

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

C32H46N7O20P3S (973.1731106000001)