<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Peng A</submitter><funding>Natural Science Foundation of Shandong Province</funding><funding>National Natural Science Foundation of China</funding><pagination>E470</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6315490</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(12)</volume><pubmed_abstract>Four angucycline glycosides including three new compounds landomycin N (&lt;b>1&lt;/b>), galtamycin C (&lt;b>2&lt;/b>) and vineomycin D (&lt;b>3&lt;/b>), and a known homologue saquayamycin B (&lt;b>4&lt;/b>), along with two alkaloids 1-acetyl-β-carboline (&lt;b>5&lt;/b>) and indole-3-acetic acid (&lt;b>6&lt;/b>), were isolated from the fermentation broth of an intertidal sediments-derived &lt;i>Streptomyces&lt;/i> sp. Their structures were established by IR, HR-ESI-MS, 1D and 2D NMR techniques. Among the isolated angucyclines, saquayamycin B (&lt;b>4&lt;/b>) displayed potent cytotoxic activity against hepatoma carcinoma cells HepG-2, SMMC-7721 and plc-prf-5, with IC&lt;sub>50&lt;/sub> values 0.135, 0.033 and 0.244 μM respectively, superior to doxorubicin. Saquayamycin B (&lt;b>4&lt;/b>) also induced apoptosis in SMMC-7721 cells as detected by its m</pubmed_abstract><journal>Marine drugs</journal><pubmed_title>Angucycline Glycosides from an Intertidal Sediments Strain &lt;i>Streptomyces&lt;/i> sp. and Their Cytotoxic Activity against Hepatoma Carcinoma Cells.</pubmed_title><pmcid>PMC6315490</pmcid><funding_grant_id>ZR2014HM018</funding_grant_id><funding_grant_id>81872771</funding_grant_id><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Xie W</pubmed_authors><pubmed_authors>Li E</pubmed_authors><pubmed_authors>Peng A</pubmed_authors><pubmed_authors>Qu X</pubmed_authors><pubmed_authors>Liu F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Angucycline Glycosides from an Intertidal Sediments Strain &lt;i>Streptomyces&lt;/i> sp. and Their Cytotoxic Activity against Hepatoma Carcinoma Cells.</name><description>Four angucycline glycosides including three new compounds landomycin N (&lt;b>1&lt;/b>), galtamycin C (&lt;b>2&lt;/b>) and vineomycin D (&lt;b>3&lt;/b>), and a known homologue saquayamycin B (&lt;b>4&lt;/b>), along with two alkaloids 1-acetyl-β-carboline (&lt;b>5&lt;/b>) and indole-3-acetic acid (&lt;b>6&lt;/b>), were isolated from the fermentation broth of an intertidal sediments-derived &lt;i>Streptomyces&lt;/i> sp. Their structures were established by IR, HR-ESI-MS, 1D and 2D NMR techniques. Among the isolated angucyclines, saquayamycin B (&lt;b>4&lt;/b>) displayed potent cytotoxic activity against hepatoma carcinoma cells HepG-2, SMMC-7721 and plc-prf-5, with IC&lt;sub>50&lt;/sub> values 0.135, 0.033 and 0.244 μM respectively, superior to doxorubicin. Saquayamycin B (&lt;b>4&lt;/b>) also induced apoptosis in SMMC-7721 cells as detected by its m</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Nov</publication><modification>2026-04-13T23:07:51.467Z</modification><creation>2019-03-26T22:36:49Z</creation></dates><accession>S-EPMC6315490</accession><cross_references><pubmed>30486371</pubmed><doi>10.3390/md16120470</doi></cross_references></HashMap>