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The chemical reactions and pathways involving aromatic compounds, any organic compound characterized by one or more planar rings, each of which contains conjugated double bonds and delocalized pi electrons, as carried out by individual cells. The chemical reactions and pathways involving ester derivatives of sinapate, (2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate. The chemical reactions and pathways resulting in the formation of aromatic derivatives of trans-cinnamic acid. The chemical reactions and pathways involving aromatic derivatives of trans-cinnamic acid. The chemical reactions and pathways resulting in many of the chemical changes of compounds that are not necessarily required for growth and maintenance of cells, and are often unique to a taxon. In multicellular organisms secondary metabolism is generally carried out in specific cell types, and may be useful for the organism as a whole. In unicellular organisms, secondary metabolism is often used for the production of antibiotics or for the utilization and acquisition of unusual nutrients. The chemical reactions and pathways involving lignans, any member of a class of plant metabolites related to lignins. Lignans are usually found as phenylpropanoid dimers in which the phenylpropanoid units are linked tail to tail and thus having a 2,3 dibenzylbutane skeleton, but higher oligomers can also exist. The chemical reactions and pathways involving ester derivatives of cinnamic acid, phenylpropenoic acid. The chemical reactions and pathways involving coumarins, compounds derived from the phenylacrylic skeleton of cinnamic acids. The chemical reactions and pathways involving cinnamic acid, 3-phenyl-2-propenoic acid. The chemical reactions and pathways involving lignins, a class of polymers of phenylpropanoid units. The chemical reactions and pathways involving ferulate, (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate. The chemical reactions and pathways involving sinapate, (2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate. The chemical reactions and pathways involving flavonoids, a group of water-soluble phenolic derivatives containing a flavan skeleton including flavones, flavonols and flavanoids, and anthocyanins. The chemical reactions and pathways involving stilbenes, a class of polyketides formed from a molecule of cinnamic acid and three molecules of malonyl-CoA. The chemical reactions and pathways involving eugenol, a colorless, aromatic, liquid hydrocarbon (C10H12O2) found in clove oil. The chemical reactions and pathways resulting in the breakdown of aromatic derivatives of trans-cinnamic acid. The chemical reactions and pathways involving coniferin, 4-(3-hydroxyprop-1-en-1-yl)-2-methoxyphenyl beta-D-glucopyranoside. The chemical reactions and pathways, including anabolism and catabolism, by which living organisms transform chemical substances. Metabolic processes typically transform small molecules, but also include macromolecular processes such as DNA repair and replication, and protein synthesis and degradation. The chemical reactions and pathways involving compounds derived from amino acids, organic acids containing one or more amino substituents. The chemical reactions and pathways involving chalcones, phenyl steryl ketone or its hydroxylated derivatives. The chemical reactions and pathways by which individual cells transform chemical substances. The chemical reactions and pathways involving amino acids, organic acids containing one or more amino substituents, and compounds derived from amino acids, as carried out by individual cells.

View Gene Ontology (GO) Term

GO TERM SUMMARY
Name: phenylpropanoid metabolic process
Acc: GO:0009698
Aspect: Biological Process
Desc: The chemical reactions and pathways involving aromatic derivatives of trans-cinnamic acid.
Synonyms:
  • phenylpropanoid metabolism
Proteins in PDR annotated with:
   This term: 16 [Search]
   Term or descendants: 187 [Search]


[geneontology.org]
INTERACTIVE GO GRAPH

GO:0009698 - phenylpropanoid metabolic process (interactive image map)
YRC Informatics Platform - Version 3.0
Created and Maintained by: Michael Riffle