Angelica tenuissima Nakai (=Ligusticum tenuissimum Kitagawa, Umbelliferae) is widely used to treat headache, diarrhea, epilepsy, and rheumatic arthralgias in oriental traditional medicine [1]. There have been phytochemical reports on various types of compounds from this plant, including phthalides, coumarins, terpenoids, and phenylpropanoids [2, 3]. Some of these compounds were found to have diverse biological activities such as antioxidative [3], anticancer [4], angiotensin converting enzyme (ACE) inhibitory [5], and antifungal [6] effects. In the present study, eight compounds, 3-butylidene-4-hydroxyphthalide (1) [7], senkyunolide B (2) [8], senkyunolide C (3) [8], wallichilide (4) [9], calycanthoside (5) [10], 2-methoxy-2-(4c-hydroxyphenyl)ethanol (6) [11], succinic acid (7) [12], and docosanoic acid (8) [13] were isolated from A. tenuissima by various chromatographic techniques. The structures of 1-8 were identified by interpretation of their 1D and 2D NMR spectroscopic data as well as by comparison with the published values. To the best of our knowledge, this is the first report on the isolation of compounds 1-8 from A. tenuissima.The dried radices of A. tenuissima (13 kg) were extracted with MeOH (3 u 18 L) overnight at room temperature. The extracts were concentrated in vacuo at 40qC to afford a MeOH-soluble residue (2.7 kg) which was dissolved in water and continuously partitioned with solvents and then concentrated to give extracts of hexanes (604 g), EtOAc (30 g), n-BuOH (116 g), and water (445 g) layer, respectively. The hexane extracts (604 g) were separated by vacuum liquid column chromatography ( 18 u 20 cm; silica gel 230-400 mesh) using gradient mixtures of EtOAc in hexanes (0.5o100%) as mobile phases, affording eight fractions (HF-01-HF-08). Compounds 8 (100 mg) and 7 (25 mg) were obtained from HF-04