Journal of Natural Products · 1999 · 135 citations · 7 references
PharmacyChemical BiologyMedicinal ChemistryDrug DesignDrug DiscoveryStructure-activity RelationshipsAntioxidant DefenseAntiviral AgentsAntiviral ImmunityAntiviral PharmacologyStructure-activity Relationship AnalysisActivitiesAntiviral Mechanisms Of ActionAntiviral Natural ProductsAntiviral Structure-activity RelationshipsComplement ModulationFree Radical ScavengingProanthocyanidin Characterization
A series of dimeric procyanidins (1-9) and some related polyphenols (10-15) were chosen as model compounds in a comparative investigation for various biological activities in order to obtain structure-activity relationships. Antiviral [herpes simplex virus (HSV) and human immunodeficiency virus (HIV)], antibacterial, superoxide radical-scavenging, and complement-modulating properties were assessed. In general, more pronounced activities were seen with epicatechin-containing dimers for anti-HSV, anti-HIV, and radical-scavenging effects, while the presence of ortho-trihydroxyl groups in the B-ring was important in compounds exhibiting anti-HSV and radical-scavenging effects and complement classical pathway inhibition. Double interflavan linkages gave rise to interesting antiviral effects (HSV and HIV) and complement inhibition. The influence of the degree of polymerization or the type of interflavan linkage (4-->6 or 4-->8) differed in the different biological systems evaluated. Only minor or moderate antibacterial effects were observed for the compounds under investigation.
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Structure and antiherpetic activity among the Tannins
Masayuki Takechi, Yasuo Tanaka, Manabu Takehara et al. · Phytochemistry · 1985 · 168 citations