Substance
ID:1818950
Names and Identifiers
IUPAC name
{[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({hydroxy[(3R)-3-hydroxy-2,2-dimethyl-3-[(2-{[2-(propanoylsulfanyl)ethyl]carbamoyl}ethyl)carbamoyl]propoxy]phosphoryl}oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid
Synonyms
propionyl-CoAPropanoyl-CoAPropionyl coenzyme APropionyl-CoAPropionyl-coenzyme AS-Propionyl-coenzym-AS-Propionylcoenzyme AS-propanoyl-CoAS-propanoyl-coenzyme Apropanoyl-coenzyme A
IUPAC Traditional name
propionyl-coa
Registration numbers
CAS Number
PubChem CID
KEGG ID
PubMed Citation Links
Reaxys Registry
BRENDA Database
4.2.1.174.1.1.316.4.1.12.7.11.22.3.1.B345.1.3.134.1.1.95.1.99.16.4.1.44.1.3.246.4.1.23.1.2.43.1.3.161.1.1.351.2.7.41.3.8.12.1.3.12.3.1.12.3.1.172.3.1.212.3.1.392.3.1.52.3.3.102.3.3.52.7.1.333.1.2.172.3.3.162.3.1.1576.4.1.32.3.1.72.8.3.12.8.3.102.3.1.82.3.1.2226.2.1.136.2.1.B112.3.1.312.3.1.2802.8.3.143.1.2.202.3.1.1362.3.1.292.3.1.42.3.1.872.3.1.822.3.1.672.3.1.1502.3.1.182.3.1.362.3.1.813.5.1.512.8.3.92.3.1.197.2.4.36.2.1.16.2.1.171.2.1.101.2.1.272.3.1.91.3.1.841.2.1.873.13.1.42.3.1.1372.3.1.1672.3.1.942.3.3.113.1.2.182.3.1.1762.3.1.1806.2.1.126.2.1.306.2.1.26.2.1.446.2.1.51.2.1.571.2.1.181.2.1.511.2.7.112.3.1.162.3.1.541.2.7.72.8.3.121.3.1.956.2.1.364.1.1.941.2.7.12.8.3.181.2.1.1043.1.2.13.1.2.22.3.1.1072.3.1.1182.3.1.1652.3.1.22.3.1.372.3.1.382.3.1.662.3.1.712.3.1.932.3.3.92.8.3.32.3.1.302.3.1.1782.3.1.482.3.1.1862.3.1.842.3.1.472.3.3.13
CompTox Database
MetaboLights Database
SABIO-RK Database
SureChEMBL Database
UniProt Database
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
Chemspider ID
FooDB Database
HMDB Database
PDBeChem Database
Wikipedia Title
Patent number
DrugBank ID
Reactom Database
UM-BBD compID
PubChem SID
Properties
No Data Available
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Molecule Details
An acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of propionic acid.
Molecular Spectra
No Data Available
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References
No Data Available
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