Procyanidin C1

Proanthocyanidin trimer

Function

Procyanidin C1 is a trimeric flavanol phytochemical composed of linked catechin and epicatechin units. It is found in cocoa, apples, grapes, cranberries, cinnamon, and additional fruits and plant-derived foods rich in condensed tannins.

Procyanidin C1 functions mainly as a polyphenolic antioxidant involved in oxidative stress modulation, endothelial signaling, inflammatory pathway interactions, and redox-sensitive vascular responses. Research has explored its effects on reactive oxygen species balance, nitric oxide pathways, antioxidant enzymes, and mitochondrial signaling.

As a larger oligomeric procyanidin, Procyanidin C1 contributes to the complex flavanol profile of cocoa and fruit-derived polyphenol systems.

Production

Plants synthesize Procyanidin C1 through flavonoid biosynthesis pathways involving polymerization of catechin and epicatechin monomers. These compounds accumulate in seeds, bark, skins, and defensive plant tissues.

Environmental stress, fruit maturity, cultivar, and processing influence concentrations. Cocoa products and grape seeds are particularly notable dietary sources.

After ingestion, Procyanidin C1 undergoes extensive microbial metabolism because of its relatively large molecular structure. Smaller phenolic metabolites generated in the intestine contribute significantly to downstream biological exposure.

Regulation

Procyanidin C1 activity is regulated by digestive metabolism, microbiome composition, food matrix interactions, and metabolite formation. Bioavailability differs from smaller flavanol monomers because of molecular size.

Research suggests Procyanidin C1 may interact with oxidative stress pathways, endothelial systems, inflammatory mediators, and vascular signaling networks. Biological effects depend on microbial conversion and tissue exposure.

Consumption from cocoa, grapes, berries, and fruits provides Procyanidin C1 together with catechins, minerals, fiber, and additional flavonoids that collectively contribute to antioxidant and vascular signaling systems.

Chemical Identity

Molecular Formula: C45H38O18
Molar Mass: 866.750 g/mol
PubChem CID: 169853

Key Biological Functions

  • Supports endothelial nitric oxide and collagen stabilization.

Key Foods / Plant Sources

Top Foods
  • Grape seeds; berries; cocoa; apples
Additional Sources
  • Fruit seed + skin tannins.

Bioavailability & Inhibitors

Inhibitor / Factor Effect on Activity / Absorption
Bioavailability depends on microbiome deglycosylation/cleavage.
Note: Factors relate to activation and cellular signaling context. Educational only.

Cellular Pathways Involved

  • NO + redox pathways (diet context).

Low Intake / Context

  • Not a classical deficiency.

Linked Cancers

  • Cardiovascular and circulatory tone (diet pattern)

Linked Ailments / Conditions

  • Capillary fragility; oxidative stress

SUMMARY OF EFFECTS ON THE BODY

  • Immune: antioxidant matrix
  • Cardiovascular: NO
  • Digestive: tannin metabolism
  • Skin: collagen stability
  • Cellular: oxidative defense