Results 281 to 290 of about 46,558 (333)
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Flavanols and Proanthocyanidins

2014
There are many kinds of natural, oligo- and polymeric materials with very specific, almost unique properties. In the field of redox active secondary metabolites, the class of ‘condensed’ polyphenolic flavonoids, often referred to as proanthocyanidins or––at higher molecular weight––as tannins clearly stands out. Such substances are found in many edible
Hadi Ebrahimnejad   +2 more
openaire   +2 more sources

Proanthocyanidins in the Apple

Journal of Food Science, 1966
SUMMARYA study was conducted on the acetone‐ and ethyl‐acetate‐extractable flavan polyphenols of Waldhöfler apples, an astringent‐tasting juice variety. The extracts were examined by cellulose thin‐layer chromatography with 5% n‐butanol and n‐butanol—acetic acid—water (BAW) as the developing solvents.
G. Senn, H. Neukom, J. P. Buren
openaire   +2 more sources

Combinatorics of proanthocyanidins in wine

The Analyst, 2019
Condensed tannin are polymers comprised of procyanidin and prodelphinidin units found in wine, chocolate, apples and many other foods.
Jonathan R. Cave, Andrew L. Waterhouse
openaire   +3 more sources

Healthy properties of proanthocyanidins

BioFactors, 2010
AbstractProanthocyanidins, also named condensed tannins, are the result of flavanols condensation. Oligomers and polymers of proanthocyanidins can widely be found in the plant kingdom, as in fruits and berries, seeds, flowers, and leafs. They have a putative role as antioxidants, and they affect the inflammatory process via calcium‐dependent release of
Noemí Boqué   +4 more
openaire   +3 more sources

Synthesis of A-type Proanthocyanidins and their Analogues. A Comprehensive Review.

Journal of Agricultural and Food Chemistry, 2020
Proanthocyanidins (PACs) are oligomers or polymers composed of units of flavanols. A-type proanthocyanidins are a subclass of PACs characterized by the presence of at least a double linkage between two consecutive monomers of flavanol.
A. Alejo-Armijo, S. Salido, J. Altarejos
semanticscholar   +1 more source

Biosynthesis of proanthocyanidins

Journal of the Chemical Society, Chemical Communications, 1975
The incorporation of 4′,5,7-trihydroxydihydroflavonol into the dimeric procyanidin B-4 in Rubus idaeus indicates that both flavan-3,4-diols and flavan-3-ols are derived biogenetically from dihydroflavonols.
Edward J. Birch, Edmon Wong
openaire   +2 more sources

Chromatography of Proanthocyanidins

1989
Current trends in chromatographic isolation and analyses of proanthocyanidins are reviewed. Preparative isolations by low pressure column chromatography can be carried out using a variety of gel types. Often, repeated separations are required to obtain pure compounds, and it has been found advantageous to alternate each separation with a different gel ...
Richard F. Helm   +4 more
openaire   +2 more sources

Grape seed proanthocyanidins suppressed macrophage foam cell formation by miRNA-9 via targeting ACAT1 in THP-1 cells.

Food & Function, 2020
Abnormal lipid metabolism in macrophages leads to atherosclerosis (AS). Excessive LDL cholesterol uptake by macrophages in the aortic endothelium leads to formation of foam cells.
D. Shao   +9 more
semanticscholar   +1 more source

Conformations of Proanthocyanidins

1992
The application of high resolution 1H-NMR and empirical (MM2, MMX) as well as semiempirical (MNDO, AMI, PM3) theoretical methods in the conformational analysis of proanthocyanidins have been the subject of much study. The E:A (B-ring equatorial or axial) ratios calculated for 4-arylflavan-3-ol model compounds, carefully selected to incorporate all ...
Richard W. Hemingway   +4 more
openaire   +2 more sources

Plant proanthocyanidins. Part II. Proanthocyanidin-A2 and its derivatives

Journal of the Chemical Society, Perkin Transactions 1, 1974
The 2,7″-epoxy-4,8″-biflavan structure (1) has been deduced for the natural proanthocyanidin-A2 on the basis of spectroscopic (13C and 1H n.m.r.) and chemical evidence. Spectroscopic data are also outlined which lead, in association with biogenetic arguments, to a proposal (1a) for the absolute stereochemistry of the natural product.
David Greatbanks   +3 more
openaire   +2 more sources

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