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[Display omitted] • Cembranoids were systematically separated by an activity-oriented approach. • Enriched the antifungal, insecticidal, and cytotoxic activities of diverse cembranoids. • Cembranoid activities might be influenced by hydroxyl groups and unsaturation. • Cembranoid kill insects by restraining acetylcholinesterase activity. • Cembranoids are promising for developing bio-pesticides and bio-medicines. Cembranoids are a class of glandular trichome exudates with a variety of structural variations and biological activities, and are found in high quantities in tobacco (Nicotiana tabacum L.). However, few studies have conducted preparative separation and examined the activities of cembranoids other than (1 S ,2 E ,4 S ,6 R ,7 E ,11 E)-2,7,11-cembratriene-4,6-diol (α -CBT-diol, 1) and (1 S ,2 E ,4 R ,6 R ,7 E ,11 E)-2,7,11-cembratriene-4,6-diol (β -CBT-diol, 2); thus, the structure-activity relationship (SAR) of cembranoids remains unclear. Here, to deduce the SAR of cembranoids, raw cembranoid extract was systematically separated through an activity-oriented approach with preparative reversed-phase liquid chromatography. Each fraction was identified, and their antifungal, insecticidal, and cytotoxic bioactivities were evaluated. Composition analysis and activity detection of primary fractions (Fr.1–Fr.10) revealed that cembranoid activity might be influenced by the number of hydroxyl groups and degree of unsaturation (macrocycle and double bonds). Sub-fraction analysis showed that the antifungal activity of cembranoids was related to the number of hydroxyl groups and double bonds, and that their cytotoxic activity was affected by the type and position of substituents. Furthermore, all four factors could influence insecticidal activity. By conducting in-depth studies of single cembranoids, their SARs were summarized. The existence of Δ11,12/Δ7,8 and hydroxylation at C-6/C-4 contributed to the antifungal activity of cembranoids. Variation in the type and position of substituents also significantly affected antifungal activity, of which Δ11,12 was the most influential factor. Additionally, the change in substituent configuration at C-4 and C-12 had no significant effect on antifungal activity. The insecticidal activity of cembranoids benefited from the existence of 4-hydroxyl, which greatly enhanced their binding affinity; however, functional groups substituted at other positions decreased insecticidal activity. Cytotoxic activity was positively correlated with α -configuration at C-4 and hydroxylation at C-6 but inversely correlated with 4-methoxy substitution. Among them, 6-hydroxyl formed the core; the α -/ β -configuration at C-12 and 4-/12-substitution of cembranoids did not affect their insecticidal activity. Insecticidal activity might play a key role by restraining acetylcholinesterase activity through hydrophobic interactions between the cembranoid carbon skeleton and residues located at the acetylcholinesterase binding pocket. These findings may provide a foundation for the development of novel cembranoid-based pesticides and medicines. [ABSTRACT FROM AUTHOR]