{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,16]],"date-time":"2026-06-16T17:12:05Z","timestamp":1781629925945,"version":"3.54.5"},"reference-count":56,"publisher":"Wiley","license":[{"start":{"date-parts":[[2025,4,1]],"date-time":"2025-04-01T00:00:00Z","timestamp":1743465600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Chemistry &amp; Biodiversity"],"abstract":"<jats:title>ABSTRACT<\/jats:title><jats:p>Fourteen phenolic compounds, comprising four sesquilignans (<jats:bold>1<\/jats:bold>\u2012<jats:bold>4<\/jats:bold>), five flavonoids (<jats:bold>5<\/jats:bold>\u2012<jats:bold>9<\/jats:bold>), two phenylethanol glycosides (<jats:bold>10<\/jats:bold> and <jats:bold>11<\/jats:bold>) together with three acylphloroglucinols (<jats:bold>12<\/jats:bold>\u2012<jats:bold>14<\/jats:bold>), were isolated from <jats:italic>Eucalyptus tereticornis<\/jats:italic>. Their structures were elucidated through spectroscopic data analyses and electronic circular dichroism (ECD) calculations. Notably, tereticornisin A (<jats:bold>1<\/jats:bold>), phloretin 2\u2032\u2010<jats:italic>O<\/jats:italic>\u2010(6\u2010deoxy\u2010\u03b2\u2010<jats:sc>d<\/jats:sc>\u2010glucopyranoside) (<jats:bold>6<\/jats:bold>), phloretin 2\u2032\u2010<jats:italic>O<\/jats:italic>\u2010(6\u2010deoxy\u2010\u03b2\u2010<jats:sc>d<\/jats:sc>\u2010galactopyranoside) (<jats:bold>7<\/jats:bold>), and 2\u2010(4\u2010hydroxyphenyl)ethyl\u2010[6\u2010<jats:italic>O<\/jats:italic>\u2010(<jats:italic>Z<\/jats:italic>)\u2010feruloyl]\u2010\u03b2\u2010<jats:sc>d<\/jats:sc>\u2010glucopyranoside (<jats:bold>10<\/jats:bold>) were new compounds. In addition, phloretin\u20102\u2032\u2010<jats:italic>O<\/jats:italic>\u2010\u03b2\u2010<jats:sc>d<\/jats:sc>\u2010xylopyranoside (<jats:bold>5<\/jats:bold>) was isolated and definitively assigned for the first time, despite its structure having been previously speculated based on HPLC\u2013UV\u2013MS\/MS analysis. Eight of the isolates displayed inhibitory activity against the ABTS free radicals with IC<jats:sub>50<\/jats:sub> values that ranged from 8.07\u00a0\u00b1\u00a00.10 to 14.41\u00a0\u00b1\u00a00.30\u00a0\u00b5M, comparable to the positive control (IC<jats:sub>50<\/jats:sub> 18.12\u00a0\u00b1\u00a00.21\u00a0\u00b5M). <jats:bold>12<\/jats:bold>\u2012<jats:bold>14<\/jats:bold> exhibited no antibacterial activity on methicillin\u2010resistant <jats:italic>Staphylococcus aureus<\/jats:italic> (MRSA) strains Newman, USA300, and Mu50, and vancomycin\u2010resistant <jats:italic>Enterococcus faecium<\/jats:italic> (VREfm) strain HS\u20100649.<\/jats:p>","DOI":"10.1002\/cbdv.202500312","type":"journal-article","created":{"date-parts":[[2025,3,17]],"date-time":"2025-03-17T12:19:11Z","timestamp":1742213951000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["New Phenolic Compounds from <i>Eucalyptus tereticornis<\/i> with Antioxidant Activity"],"prefix":"10.1002","author":[{"given":"Yu","family":"Zhang","sequence":"first","affiliation":[{"name":"Shandong Laboratory of Yantai Drug Discovery, Bohai Rim Advanced Research Institute for Drug Discovery  Yantai People's Republic of China"},{"name":"Shanghai Institute of Materia Medica, Chinese Academy of Sciences  Shanghai People's Republic of China"},{"name":"Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University  Chongqing People's Republic of China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lei","family":"Miao","sequence":"additional","affiliation":[{"name":"Shandong Laboratory of Yantai Drug Discovery, Bohai Rim Advanced Research Institute for Drug Discovery  Yantai People's Republic of China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Guo\u2010Li","family":"Li","sequence":"additional","affiliation":[{"name":"Chongqing Key Laboratory of Development and Utilization of Genuine Medicinal Materials in Three Gorges Reservoir Area, Chongqing Three Gorges Medical College  Chongqing People's Republic of China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0376-0369","authenticated-orcid":false,"given":"Chuan\u2010Rui","family":"Zhang","sequence":"additional","affiliation":[{"name":"Shandong Laboratory of Yantai Drug Discovery, Bohai Rim Advanced Research Institute for Drug Discovery  Yantai People's Republic of China"},{"name":"Shanghai Institute of Materia Medica, Chinese Academy of Sciences  Shanghai People's Republic of China"},{"name":"Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University  Chongqing People's Republic of China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2025,4]]},"reference":[{"key":"e_1_2_9_2_1","first-page":"321","volume-title":"Flora of China (Zhongguo Zhiwu Zhi)","author":"Chen J.","year":"2007"},{"key":"e_1_2_9_3_1","doi-asserted-by":"crossref","first-page":"907","DOI":"10.1002\/cbdv.201400327","article-title":"Botanical, Phytochemical, and Anticancer Properties of the Eucalyptus Species","volume":"12","author":"Vuong Q. 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