{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T13:03:25Z","timestamp":1792155805511,"version":"4.4.0"},"reference-count":110,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2013,2,20]],"date-time":"2013-02-20T00:00:00Z","timestamp":1361318400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["bpspubs.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["British J Pharmacology"],"published-print":{"date-parts":[[2013,3]]},"abstract":"<jats:p>\n                    The consumption of green tea (\n                    <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>\n                    <jats:italic>amellia sinensis<\/jats:italic>\n                    ) has been shown to have many physiological and pharmacological health benefits. In the past two decades several studies have reported that epigallocatechin\u20103\u2010gallate (\n                    <jats:styled-content style=\"fixed-case\">EGCG<\/jats:styled-content>\n                    ), the main constituent of green tea, has anti\u2010infective properties. Antiviral activities of\n                    <jats:styled-content style=\"fixed-case\">EGCG<\/jats:styled-content>\n                    with different modes of action have been demonstrated on diverse families of viruses, such as\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">R<\/jats:styled-content>\n                      etroviridae\n                    <\/jats:italic>\n                    ,\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">O<\/jats:styled-content>\n                      rthomyxoviridae\n                    <\/jats:italic>\n                    and\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">F<\/jats:styled-content>\n                      laviviridae\n                    <\/jats:italic>\n                    and include important human pathogens like human immunodeficiency virus, influenza\n                    <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>\n                    virus and the hepatitis\n                    <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>\n                    virus. Furthermore, the molecule interferes with the replication cycle of\n                    <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content>\n                    viruses like hepatitis\n                    <jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>\n                    virus, herpes simplex virus and adenovirus. Most of these studies demonstrated antiviral properties within physiological concentrations of\n                    <jats:styled-content style=\"fixed-case\">EGCG<\/jats:styled-content>\n                    \u2005\n                    <jats:italic>in vitro<\/jats:italic>\n                    . In contrast, the minimum inhibitory concentrations against bacteria were 10\u2013100\u2010fold higher. Nevertheless, the antibacterial effects of\n                    <jats:styled-content style=\"fixed-case\">EGCG<\/jats:styled-content>\n                    alone and in combination with different antibiotics have been intensively analysed against a number of bacteria including multidrug\u2010resistant strains such as methicillin\u2010resistant\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>\n                      taphylococcus aureus\n                    <\/jats:italic>\n                    or\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>\n                      tenotrophomonas maltophilia\n                    <\/jats:italic>\n                    . Furthermore, the catechin\n                    <jats:styled-content style=\"fixed-case\">EGCG<\/jats:styled-content>\n                    has antifungal activity against human\u2010pathogenic yeasts like\n                    <jats:italic>\n                      <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>\n                      andida albicans\n                    <\/jats:italic>\n                    . Although the mechanistic effects of\n                    <jats:styled-content style=\"fixed-case\">EGCG<\/jats:styled-content>\n                    are not fully understood, there are results indicating that\n                    <jats:styled-content style=\"fixed-case\">EGCG<\/jats:styled-content>\n                    binds to lipid membranes and affects the folic acid metabolism of bacteria and fungi by inhibiting the cytoplasmic enzyme dihydrofolate reductase. This review summarizes the current knowledge and future perspectives on the antibacterial, antifungal and antiviral effects of the green tea constituent\n                    <jats:styled-content style=\"fixed-case\">EGCG<\/jats:styled-content>\n                    .\n                  <\/jats:p>","DOI":"10.1111\/bph.12009","type":"journal-article","created":{"date-parts":[[2012,10,17]],"date-time":"2012-10-17T00:02:16Z","timestamp":1350432136000},"page":"1059-1073","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":515,"title":["Anti\u2010infective properties of epigallocatechin\u20103\u2010gallate (\n                    <scp>EGCG<\/scp>\n                    ), a component of green tea"],"prefix":"10.1111","volume":"168","author":[{"given":"J","family":"Steinmann","sequence":"first","affiliation":[{"name":"Institute of Medical Microbiology University Hospital Essen University of Duisburg\u2010Essen  Essen 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