<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen M</submitter><funding>National Natural Science Foundation of China</funding><pagination>E146</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4999907</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(8)</volume><pubmed_abstract>Three new polyhydroxylated sterol derivatives topsensterols A-C (1-3) have been isolated from a marine sponge Topsentia sp. collected from the South China Sea. Their structures were elucidated by detailed analysis of the spectroscopic data, especially the NOESY spectra. Topsensterols A-C (l-3) possess novel 2β,3α,4β,6α-tetrahydroxy-14α-methyl Δ(9(11)) steroidal nuclei with unusual side chains. Compound 2 exhibited cytotoxicity against human gastric carcinoma cell line SGC-7901 with an IC50 value of 8.0 μM. Compound 3 displayed cytotoxicity against human erythroleukemia cell line K562 with an IC50 value of 6.0 μM.</pubmed_abstract><journal>Marine drugs</journal><pubmed_title>Topsensterols A-C, Cytotoxic Polyhydroxylated Sterol Derivatives from a Marine Sponge Topsentia sp.</pubmed_title><pmcid>PMC4999907</pmcid><funding_grant_id>U1406402-1</funding_grant_id><funding_grant_id>41322037</funding_grant_id><funding_grant_id>41130858</funding_grant_id><pubmed_authors>Wu XD</pubmed_authors><pubmed_authors>Wang CY</pubmed_authors><pubmed_authors>Chen M</pubmed_authors><pubmed_authors>Zhao Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Topsensterols A-C, Cytotoxic Polyhydroxylated Sterol Derivatives from a Marine Sponge Topsentia sp.</name><description>Three new polyhydroxylated sterol derivatives topsensterols A-C (1-3) have been isolated from a marine sponge Topsentia sp. collected from the South China Sea. Their structures were elucidated by detailed analysis of the spectroscopic data, especially the NOESY spectra. Topsensterols A-C (l-3) possess novel 2β,3α,4β,6α-tetrahydroxy-14α-methyl Δ(9(11)) steroidal nuclei with unusual side chains. Compound 2 exhibited cytotoxicity against human gastric carcinoma cell line SGC-7901 with an IC50 value of 8.0 μM. Compound 3 displayed cytotoxicity against human erythroleukemia cell line K562 with an IC50 value of 6.0 μM.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Aug</publication><modification>2025-04-04T11:56:03.656Z</modification><creation>2019-03-27T02:22:44Z</creation></dates><accession>S-EPMC4999907</accession><cross_references><pubmed>27490555</pubmed><doi>10.3390/md14080146</doi></cross_references></HashMap>