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Plant sesterterpenoids are an extremely rare family of natural products that generally possess novel chemical structures and diverse biological activities. Herein, we report the discovery of an unprecedented group of minor plant sesterterpenoids, gracilisoids B-E (2-5), which feature two types of highly functionalized bicyclo[3.2.0]heptane carbon skeletons, along with their biogenetically related precursor gracilisoid A (1), from a Lamiaceae ethnomedicinal plant, Eurysolen gracilis. To confirm their structures and obtain adequate materials for biological research, the asymmetric total syntheses of gracilisoids A-E (1-5) and four new biogenetically-related congeners gracilisoids F-I (6-9) were achieved from commercially available (-)-citronellal by a bioinspired approach that involves a Norrish-Yang photocyclization/α-hydroxy ketone rearrangement tandem reaction and a late-stage biomimetic photooxidation as key steps. Biological investigations revealed that gracilisoids A-I (1-9) significantly inhibited IFN-γ production and/or T cell proliferation probably through inhibition of the STAT pathway. The findings herald the potential of these gracilisoids as novel immunosuppressive agents, and efficient synthetic approaches will facilitate a comprehensive evaluation of their value in future drug development., (© 2025 Wiley-VCH GmbH.)