Procyanidin C2 is found in grape seeds and wine, in barley, malt and beer, in Betula spp., in Pinus radiata, in Potentilla viscosa, in Salix caprea or in Cryptomeria japonica. The contents in barley grain of trimeric proanthocyanidins, including procyanidin C2, range from 53 to 151 μg catechin equivalents/g.
Possible health uses
Proanthocyanidin oligomers, extracted from grape seeds, have been used for the experimental treatment of androgenic alopecia. When applied topically, they promote hair growthin vitro, and induce anagenin vivo. Procyanidin C2 is the subtype of extract most effective. Experiments showed that both procyanidin C2 and Pycnogenol increase TNF-α secretion in a concentration- and time-dependent manner. These results demonstrate that procyanidins act as modulators of the immune response in macrophages.
Chemistry
In the presence of procyanidin C2, the red color of the anthocyanin oenin appears more stable. However, the HPLC chromatogram shows a decrease in the amplitude of the peaks of oenin and procyanidin C2. Concomitantly, a new peak appears with a maximal absorption in the red region. This newly formed pigment probably comes from the condensation of oenin and procyanidin C2.
Chemical synthesis
A stereoselective synthesis of benzylated catechin trimer under intermolecular condensation is achieved using equimolar amount of dimeric catechin nucleophile and monomeric catechin electrophile catalyzed by AgOTf or AgBF4. The coupled product can be transformed into procyanidin C2 by a known procedure. The stereoselective synthesis of seven benzylated proanthocyanidin trimers -epicatechin--epicatechin trimer, catechin--catechin--catechin trimer, epicatechin--epicatechin--catechin trimer and epicatechin--catechin- can be achieved with TMSOTf-catalyzed condensation reaction, in excellent yields. The structure of benzylated procyanidin C2 was confirmed by comparing the 1H NMR spectra of protected procyanidin C2 that was synthesized by two different condensation approaches. Finally, deprotection of -catechin and -epicatechin trimers derivatives gives four natural procyanidin trimers in good yields. Molar equivalents of synthetic -leucocyanidin and -catechin condense with exceptional rapidity at pH 5 under ambient conditions to give the all-trans-- and -bi- the all-trans-- and -tri-.
A coupling utilising a C8-boronic acid as a directing group was developed in the synthesis of natural procyanidin B3 -catechin-4α→8-. The key interflavan bond is forged using a Lewis acid-promoted coupling of C4-ether with C8-boronic acid to provide the α-linked dimer with high diastereoselectivity. Through the use of a boron protecting group, the coupling procedure can be extended to the synthesis of a protected procyanidin trimer analogous to natural procyanidin C2.
