Journal of Natural Products · 2004 · 27 citations · 8 references
Life SciencesBotanyPharmacologyOrganic ChemistryPlant BiochemistryStructure-activity RelationshipsAntibacterial AgentsMedicinal PlantsStructure-activity Relationship AnalysisAbsolute Configuration DeterminationBioactive ConstituentsChemical TransformationMinimum Inhibitory Concentration DeterminationMinimum Inhibitory Concentration TestingMycobacterium Tuberculosis Infection
Two new sesquiterpenoids, (1S,4S,5R,10R)-1-hydroxy-6-isobutyryloxy-10H-9-oxofuranoeremophilane (1) and 1alpha-hydroxy-6beta-(2xi-methylbutyryloxy)-10alphaH-9-oxofuranoeremophilane (2), along with 21 known constituents, were isolated from the n-hexane and dichloromethane extracts of the above-ground biomass and roots of Senecio chionophilus. The structures of 1 and 2 were elucidated on the basis of spectroscopic evidence and chemical transformation methods. The absolute configuration of 1 was determined by Mosher ester methodology. All of the isolates were evaluated for their antitubercular potential against Mycobacterium tuberculosis in a microplate Alamar Blue assay. Compound 2, 6beta-angeloyloxy-1alpha-hydroxy-10alphaH-9-oxofuranoeremophilane (3), and 4'-hydroxyacetophenone (6) exhibited mild antitubercular activity at minimum inhibitory concentrations of 119, 114, and 121 microg/mL, respectively.
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L A Collins, Scott G. Franzblau · Antimicrobial Agents and Chemotherapy · 1997 · 1.6K citations · Full text
Veterinary Medicine, Infectious Diseases, Antimicrobial Pharmacology +7
Studies on sesquiterpenoids—IX
Hiroshi Ishii, Takehiko Tozyo, Hideo Minato · Tetrahedron · 1965 · 68 citations
Goh Miyajima, Yoshio Sasaki, Miyoko Suzuki · Chemical and Pharmaceutical Bulletin · 1971 · 39 citations · Full text