Journal of the American Chemical Society · 2003 · 109 citations · 6 references
MedicineMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsAntibacterial PharmacologyAntitumor AntibioticsConjugation ReactionsStructure-activity Relationship AnalysisAntibiotic DiscoveryAntitumor Antibiotic BiosynthesisCarbohydrate-derived AntibioticsConjugationCytotoxicity AssaysEnediyne AntibioticsMass Spectral Data Analysis
Three new compounds of the enediyne antibiotics, shishijimicins A-C (1-3), have been isolated from the ascidian Didemnum proliferum. They encompass a novel sugar component, which is a conjugation product of a hexose and a beta-carboline, attached to the calicheamicinone aglycone. Their structures have been determined by interpretation of spectral data. Shishijimicins showed extremely potent cytotoxicity against HeLa cells with IC(50) values of 1.8-6.9 pM.
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John N. Haseltine, Maria Paz Cabal, Nathan B. Mantlo et al. · Journal of the American Chemical Society · 1991 · 107 citations
Luigi Gomez Paloma, Jarrod A. Smith, Walter Chazin et al. · Journal of the American Chemical Society · 1994 · 99 citations