Figure 1
From: Genome mining and biosynthesis of fumitremorgin-type alkaloids in ascomycetes
Structures of prenylated indole alkaloids derived from cyclo-L-tryptophan–L-proline and their biosynthetic relationship: brevianamide F (1), tryprostatins B (2) and A (3), spirotryprostatins B (4) and A (5), cyclotryprostatin C (6), demethoxyfumitremorgin C (7), fumitremorgin C (8), fumitremorgins B (9) and A (10), verruculogen (11), deoxybrevianamide E (12), brevianamide A (13), austamide (14) and notoamide A (15).
