Page last updated: 2024-08-25

epicatechin and proanthocyanidin a2

epicatechin has been researched along with proanthocyanidin a2 in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chang, JJ; Kashiwada, Y; Lee, KH; Nishioka, I; Nonaka, G1
De Bruyne, T; De Clercq, E; Pieters, L; Vanden Berghe, D; Vlietinck, AJ; Witvrouw, M1
Foo, LY; Howell, AB; Lu, Y; Vorsa, N1
Chou, CJ; Kuo, YC; Lin, LC1
Arnhold, J; Flemmig, J; Gau, J; Prévost, M; Rodewald, S; Sarosi, MB; Van Antwerpen, P1

Other Studies

5 other study(ies) available for epicatechin and proanthocyanidin a2

ArticleYear
Antitumor agents, 129. Tannins and related compounds as selective cytotoxic agents.
    Journal of natural products, 1992, Volume: 55, Issue:8

    Topics: Antineoplastic Agents, Phytogenic; Biflavonoids; Catechin; Cell Survival; Plants, Medicinal; Proanthocyanidins; Tannins; Tumor Cells, Cultured

1992
Biological evaluation of proanthocyanidin dimers and related polyphenols.
    Journal of natural products, 1999, Volume: 62, Issue:7

    Topics: Anthocyanins; Anti-Bacterial Agents; Anti-HIV Agents; Anti-Infective Agents; Antiviral Agents; Bacteria; Complement Inactivator Proteins; Euphorbiaceae; Flavonoids; Free Radical Scavengers; Hemolysis; Magnetic Resonance Spectroscopy; Microbial Sensitivity Tests; Peru; Phenols; Plants, Medicinal; Polymers; Simplexvirus

1999
A-Type proanthocyanidin trimers from cranberry that inhibit adherence of uropathogenic P-fimbriated Escherichia coli.
    Journal of natural products, 2000, Volume: 63, Issue:9

    Topics: Anthocyanins; Bacterial Adhesion; Biflavonoids; Catechin; Escherichia coli; Fruit; Humans; Molecular Structure; Proanthocyanidins; Urinary Bladder; Urinary Tract Infections

2000
Immunomodulatory proanthocyanidins from Ecdysanthera utilis.
    Journal of natural products, 2002, Volume: 65, Issue:4

    Topics: Adjuvants, Immunologic; Anthocyanins; Apocynaceae; Biflavonoids; Catechin; Dose-Response Relationship, Drug; Humans; Interferon-gamma; Interleukin-2; Leukocytes, Mononuclear; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Phytohemagglutinins; Plant Lectins; Plant Stems; Plants, Medicinal; Proanthocyanidins; Spectrophotometry, Infrared; Spectrophotometry, Ultraviolet; Structure-Activity Relationship; Taiwan

2002
Tannins and Tannin-Related Derivatives Enhance the (Pseudo-)Halogenating Activity of Lactoperoxidase.
    Journal of natural products, 2017, 05-26, Volume: 80, Issue:5

    Topics: Halogenation; Hydrogen Peroxide; Hydrolyzable Tannins; Kinetics; Lactoperoxidase; Molecular Structure; Nitrobenzoates; Oxidation-Reduction; Plant Extracts; Proanthocyanidins; Rhizome; Sulfhydryl Compounds; Tannins; Thiocyanates

2017