Granulatimide and isogranulatimide, aromatic alkaloids with G2 checkpoint inhibition activity isolated from the Brazilian ascidian Didemnum granulatum:: Structure elucidation and synthesis
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Berlinck, RGS
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机构:Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
Berlinck, RGS
Britton, R
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机构:Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
Britton, R
Piers, E
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机构:Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
Piers, E
Lim, L
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机构:Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
Lim, L
Roberge, M
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机构:Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
Roberge, M
da Rocha, RM
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机构:Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
da Rocha, RM
Andersen, RJ
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机构:Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
Andersen, RJ
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[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
[2] Univ British Columbia, Dept Earth & Ocean Sci, Vancouver, BC V6T 1Z1, Canada
[3] Univ British Columbia, Dept Biochem & Mol Biol, Vancouver, BC V6T 1Z3, Canada
Crude methanol ex-tracts of the ascidian Didemum granulatum collected in Brazil showed activity in a new screen for G2 cell cycle checkpoint inhibitors. Bioassay-guided fractionation of the extract yielded the known alkaloids didemnimides A (1) and D (2), the new alkaloid didemnimide E (3), and a new G2 checkpoint inhibitor. Two candidate structures for the inhibitor, named granulatimide (4) and isogranulatimide (5), have been prepared via a short and efficient biomimetic synthesis involving the photolysis of didemnimide A (1). The synthesis revealed that the correct structure for the naturally occurring G2 checkpoint inhibitor is isogranulatimide (5). Granulatimide (4), the other candidate structure, was also found to be a G2 checkpoint inhibitor, and it was subsequently detected in chromatographic fractions associated with purification of D. granulatum alkaloids. Granulatimide (4) and isogranulatimide (5) represent the first examples of a new class of G2 specific cell cycle checkpoint inhibitors and the first ones identified through a rational screening program.