<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Torres-Mendoza D</submitter><funding>Global Environmental Fund</funding><funding>Fogarty International Center’s International Cooperative Biodiversity Groups program</funding><funding>Fogarty International Center's International Cooperative Biodiversity Groups program</funding><funding>National System of Investigators (SNI)</funding><funding>Secretaría Nacional de Ciencia, Tecnología e Innovación</funding><pagination>E2179</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6225264</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(9)</volume><pubmed_abstract>Chemical examination of the octocoral-associated &lt;i>Bacillus&lt;/i> species (sp.) DT001 led to the isolation of pumilacidins A (&lt;b>1&lt;/b>) and C (&lt;b>2&lt;/b>). We investigated the effect of these compounds on the viability of &lt;i>Plasmodium falciparum&lt;/i> and the mechanism of pumilacidin-induced death. The use of inhibitors of protein kinase C (PKC) and phosphoinositide 3-kinase (PI3K) was able to prevent the effects of pumilacidins A and C. The results indicated also that pumilacidins inhibit parasite growth via mitochondrial dysfunction and decreased cytosolic Ca&lt;sup>2+&lt;/sup>.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Pumilacidins from the Octocoral-Associated &lt;i>Bacillus&lt;/i> sp. DT001 Display Anti-Proliferative Effects in &lt;i>Plasmodium falciparum&lt;/i>.</pubmed_title><pmcid>PMC6225264</pmcid><funding_grant_id>TW006634</funding_grant_id><funding_grant_id>81860</funding_grant_id><funding_grant_id>170-2016</funding_grant_id><funding_grant_id>COL09-047</funding_grant_id><pubmed_authors>Guzman HM</pubmed_authors><pubmed_authors>Torres-Mendoza D</pubmed_authors><pubmed_authors>Gutierrez M</pubmed_authors><pubmed_authors>Pineda LM</pubmed_authors><pubmed_authors>Dorrestein PC</pubmed_authors><pubmed_authors>Spadafora C</pubmed_authors><pubmed_authors>Coronado LM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pumilacidins from the Octocoral-Associated &lt;i>Bacillus&lt;/i> sp. DT001 Display Anti-Proliferative Effects in &lt;i>Plasmodium falciparum&lt;/i>.</name><description>Chemical examination of the octocoral-associated &lt;i>Bacillus&lt;/i> species (sp.) DT001 led to the isolation of pumilacidins A (&lt;b>1&lt;/b>) and C (&lt;b>2&lt;/b>). We investigated the effect of these compounds on the viability of &lt;i>Plasmodium falciparum&lt;/i> and the mechanism of pumilacidin-induced death. The use of inhibitors of protein kinase C (PKC) and phosphoinositide 3-kinase (PI3K) was able to prevent the effects of pumilacidins A and C. The results indicated also that pumilacidins inhibit parasite growth via mitochondrial dysfunction and decreased cytosolic Ca&lt;sup>2+&lt;/sup>.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Aug</publication><modification>2026-04-30T09:19:28.085Z</modification><creation>2019-03-27T00:07:16Z</creation></dates><accession>S-EPMC6225264</accession><cross_references><pubmed>30158478</pubmed><doi>10.3390/molecules23092179</doi></cross_references></HashMap>