Page last updated: 2024-11-08

cinnamoyl-coenzyme a

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

(E)-cinnamoyl-CoA : The (E)-isomer of cinnamoyl-CoA. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID6444037
CHEBI ID15463
CHEBI ID10956
SCHEMBL ID418552
MeSH IDM0079563

Synonyms (33)

Synonym
benzylideneacetyl-coa
3-phenylacryloyl-coenzyme a
3-phenylacryloyl-coa
benzylideneacetyl-coenzyme a
beta-phenylacryloyl-coa
3'-phosphoadenosine 5'-{3-[(3r)-3-hydroxy-2,2-dimethyl-4-oxo-4-{[3-oxo-3-({2-[(3-phenylprop-2-enoyl)sulfanyl]ethyl}amino)propyl]amino}butyl] dihydrogen diphosphate}
3-phenylprop-2-enoyl-coenzyme a
cinnamoyl-coenzyme a
CHEBI:15463
beta-phenylacryloyl-coenzyme a
3'-phosphoadenosine 5'-{3-[(3r)-3-hydroxy-2,2-dimethyl-4-oxo-4-({3-oxo-3-[(2-{[(2e)-3-phenylprop-2-enoyl]sulfanyl}ethyl)amino]propyl}amino)butyl] dihydrogen diphosphate}
(e)-cinnamoyl-coa
coenzyme a, s-(3-phenyl-2-propenoate), (e)-
CHEBI:10956
76109-04-1
C00540
s-(cinnamoyl) coenzyme a
cinnamoyl-coa ,
s-[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]ethyl] (e)-3-phenylprop-2-enethioate
6yvq9p5rat ,
unii-6yvq9p5rat
coenzyme a, cinnamoyl-
coenzyme a,s-[(2e)-3-phenyl-2-propenoate]
SCHEMBL418552
s-[2-[3-[[(2r)-4-[[[(2r,3s,4r,5r)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-2-hydroxy-3,3-dimethyl-butanoyl]amino]propanoylamino]ethyl] (e)-3-phenylprop-2-enethioate
3-phenyl-2e-propenoyl-coa
LMFA07050294
Q2972823
DTXSID501030398
coenzyme a, s-((2e)-3-phenyl-2-propenoate)
s-(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)ethyl)(e)-3-phenylprop-2-enethioate
30801-99-1
coenzyme a, s-(3-phenyl-2-propenoate)
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
cinnamoyl-CoAAn acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of cinnamic acid.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (5)

PathwayProteinsCompounds
Flavonoid Biosynthesis1150
Stilbenoid, Diarylheptanoid, and Gingerol Biosynthesis417
Flavonoid biosynthesis019
Serotonin biosynthesis112
Pinobanksin biosynthesis19
Salicylate biosynthesis116

Research

Studies (20)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (5.00)18.7374
1990's5 (25.00)18.2507
2000's8 (40.00)29.6817
2010's5 (25.00)24.3611
2020's1 (5.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other20 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]