<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>64(Pt 2)</volume><submitter>Brito I</submitter><pubmed_abstract>AROMATICINE (SYSTEMATIC NAME: 4a,8-dimethyl-3-methyl-ene-3,3a,4,4a,7a,8,9,9a-octa-hydro-azuleno[6,5-b]furan-2,5-dione), C(15)H(18)O(3), is a natural lactone isolated from Amblyopappus pusillus. The mol-ecular structure and conformation agree with the results of Romo, Joseph-Nathan &amp; Díaz [(1964 ▶). Tetra-hedron, 20, 79-85]. The fused-ring system contains a seven-membered ring in a twist-boat conformation and two five-membered rings trans fused in envelope conformations.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o529</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2960399</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Aromaticine, a sesquiterpene lactone from Amblyopappus pusillus.</pubmed_title><pmcid>PMC2960399</pmcid><pubmed_authors>Lopez-Rodriguez M</pubmed_authors><pubmed_authors>Borquez J</pubmed_authors><pubmed_authors>Loyola LA</pubmed_authors><pubmed_authors>Brito I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aromaticine, a sesquiterpene lactone from Amblyopappus pusillus.</name><description>AROMATICINE (SYSTEMATIC NAME: 4a,8-dimethyl-3-methyl-ene-3,3a,4,4a,7a,8,9,9a-octa-hydro-azuleno[6,5-b]furan-2,5-dione), C(15)H(18)O(3), is a natural lactone isolated from Amblyopappus pusillus. The mol-ecular structure and conformation agree with the results of Romo, Joseph-Nathan &amp; Díaz [(1964 ▶). Tetra-hedron, 20, 79-85]. The fused-ring system contains a seven-membered ring in a twist-boat conformation and two five-membered rings trans fused in envelope conformations.</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Jan</publication><modification>2025-04-18T12:26:53.223Z</modification><creation>2019-03-26T23:59:51Z</creation></dates><accession>S-EPMC2960399</accession><cross_references><pubmed>21201548</pubmed><doi>10.1107/S1600536808002729</doi></cross_references></HashMap>