Journal of Natural Products · 2009 · 39 citations · 11 references
Life SciencesBiochemistryBiologyDrug DiscoveryInsect PhysiologyStructure-activity RelationshipsBioinorganic ChemistryBiomolecular StructureMetabolite IdentificationStructure-activity Relationship AnalysisChirality Determination
Angiopterlactones A (1) and B (2), two unique lactones, and three known lactones, osmundalactone (3), osmundalin (4), and 3,5-dihydroxy-gamma-caprolactone (5), have been isolated from the rhizome of Angiopteris caudatiformis. The structures of 1 and 2 were determined by NMR and MS methods, and the structure of 2 was confirmed by X-ray crystallography. The absolute configurations of 1 and 2 were assigned by application of the CD excitation chirality method and the modified Mosher's method. Compound 1 was slightly cytotoxic against HeLa cells, with an IC(50) value of 68.8 microM, and compounds 3 and 4 showed moderate insect antifeeding activity against Plutella xylostella and Heliothis virescens.
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Chinnaperumal Kamaraj, Abdul Abdul Rahuman, Asokan Bagavan · Parasitology Research · 2008 · 77 citations
Optical activity and lactone ring configurations
A.F. Beecham · Tetrahedron Letters · 1968 · 58 citations
Meroditerpenoids from the Brown Alga <i>Sargassum siliquastrum</i>
Misong Jung, Kyoung Hwa Jang, Bora Kim et al. · Journal of Natural Products · 2008 · 57 citations · Full text
The orthosomycin family of antibiotics—I
W. David Ollis, Christopher Smith, Derek E. Wrigth · Tetrahedron · 1979 · 55 citations