<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li T</submitter><funding>National Natural Science Foundation of China</funding><funding>Natural Science Foundation of Guangdong Province</funding><pagination>29376-29384</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9040573</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(47)</volume><pubmed_abstract>Eight previously undescribed diarylheptanoids (1-8), together with fifteen known analogues (9-23), were isolated from the rhizomes of &lt;i>Zingiber officinale&lt;/i>. Their structures were unambiguously determined by comprehensive spectroscopic analyses and electronic circular dichroism (ECD) calculations. It is worth mentioning that 1-3 are the first reported structures of diaryl ether heptanoids in &lt;i>Z. officinale&lt;/i>, whereas 15-17 were isolated from &lt;i>Zingiber&lt;/i> for the first time. Furthermore, a gene enrichment analysis of the interacting targets indicated that diarylheptanoids were mainly associated with the anti-tumor activity by affecting DNA damage signaling pathway. The results showed that 6, 16-19 had remarkable inhibitory effects against five tumor cell lines (A549, HepG2, HeLa,</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Diarylheptanoid analogues from the rhizomes of &lt;i>Zingiber officinale&lt;/i> and their anti-tumour activity.</pubmed_title><pmcid>PMC9040573</pmcid><funding_grant_id>2018A030313707</funding_grant_id><funding_grant_id>81803347</funding_grant_id><pubmed_authors>Pang QQ</pubmed_authors><pubmed_authors>Zhou M</pubmed_authors><pubmed_authors>Yao XJ</pubmed_authors><pubmed_authors>Li HB</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Pan DB</pubmed_authors><pubmed_authors>Yao XS</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Diarylheptanoid analogues from the rhizomes of &lt;i>Zingiber officinale&lt;/i> and their anti-tumour activity.</name><description>Eight previously undescribed diarylheptanoids (1-8), together with fifteen known analogues (9-23), were isolated from the rhizomes of &lt;i>Zingiber officinale&lt;/i>. Their structures were unambiguously determined by comprehensive spectroscopic analyses and electronic circular dichroism (ECD) calculations. It is worth mentioning that 1-3 are the first reported structures of diaryl ether heptanoids in &lt;i>Z. officinale&lt;/i>, whereas 15-17 were isolated from &lt;i>Zingiber&lt;/i> for the first time. Furthermore, a gene enrichment analysis of the interacting targets indicated that diarylheptanoids were mainly associated with the anti-tumor activity by affecting DNA damage signaling pathway. The results showed that 6, 16-19 had remarkable inhibitory effects against five tumor cell lines (A549, HepG2, HeLa,</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-04-22T07:48:22.77Z</modification><creation>2025-04-05T22:18:30.256Z</creation></dates><accession>S-EPMC9040573</accession><cross_references><pubmed>35479564</pubmed><doi>10.1039/d1ra03592d</doi></cross_references></HashMap>