Cytotoxic Spliceostatin Analogs from Pseudomonas sp
- PMID: 31298476
- DOI: 10.1002/cbdv.201900266
Cytotoxic Spliceostatin Analogs from Pseudomonas sp
Abstract
Two new spliceostatin analogs, designed as spliceostatins J and K (1 and 2), were isolated and identified from the culture of Pseudomonas sp., along with two known ones, FR901464 (3) and spliceostatin E (4). Their structures were elucidated by detailed interpretation of their spectroscopic data, especially 2D-NMR and HR-ESI-MS. Spliceostatin J (1) represented the first example of spliceostatins bearing an unusual hexahydrofuro[3,4-b]furan moiety. Biological assay showed all the isolated compounds except 1 displayed potent cytotoxic activities against two cancer cell lines (MDA-MB-231 and A-549). Structure-activity-relationship studies revealed that the tetrahydropyran ring in spliceostatin analogs was necessary for their bioactive retention.
Keywords: Pseudomonas; bacteria; biological activity; cytotoxicity; spliceostatin.
© 2019 Wiley-VHCA AG, Zurich, Switzerland.
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