Seven sesquiterpenoids, including a clovane-phenylpropanoid hybrid (1), a clovane-menthane hybrid (2) and five linear ones incorporating a tetrahydrofuran ring (36 & 8), along with four steroids (7 & 911), were obtained from the ethanolic extract of a well-known aromatic and medicinal herb Eupatorium fortunei. Their structures were characterized by detailed analyses of spectroscopic data and comparison with known analogues, with seven (17) of them being described for the first time. Compounds 1 and 2 represent the first examples of clovane type sesquiterpenoids hybridizing with other class of natural products, and this is also the first record of linear sesquiterpenyl constituents (36 & 8) from the title species. All the isolates were evaluated for their inhibitory effect on NO production induced by LPS in murine RAW264.7 macrophage cells, and 1, 7, 10 and 11 exhibited moderate activity with IC50 values in the range of 24.443.5 M.