In the course of our characterization studies on the bioactive saponin constituents from Camellia (C.) sinensis (Theaceae), we have reported the isolation and structure elucidation of theasaponins A 1 -A 5 , C 1 , E 1 -E 13 , F 1 -F 3 , G 1 , G 2 , and H 1 , 2-6) assamsaponins A-I, 7,8) and camelliasaponins B 1 and C 1 9) from the seeds of Japanese C. sinensis (L.) O. KUNTZE and Sri Lankan C. sinensis L. var. assamica PERRE, and foliatheasaponins I-V 10) from the leaves of Japanese C. sinensis. Among the saponin constituents, theasaponin E 1 showed antisweet activity, 2) while theasaponins A 2 , E 1 , E 2 , and E 5 and assamsaponins A, C, and D were found to exhibit potent inhibitory effects on gastric lesions in rats. 4,5) In addition, floratheasaponins A-C (1-3) were isolated from the flower buds of Japanese C. sinensis and these acylated polyhydroxyoleanane-type triterpene oligoglycosides showed inhibitory effects on serum triglyceride elevation in olive oil-treated mice.11) As a continuation of our studies on bioactive constituents of medicinal flowers, 1,11-13) the methanolic extract of the flower buds of Chinese C. sinensis was found to inhibit an immediate allergic reaction by monitoring the release of b-hexosaminidase from rat basophilic leukemia (RBL-2H3) cells. From the methanolic extract, we have isolated six new acylated oleanane-type triterpene oligoglycosides, floratheasaponins D (4), E (5), F (6), G (7), H (8), and I (9), together with 21 known compounds including floratheasaponins A-C (1-3). Furthermore, we examined the inhibitory effects of principal floratheasaponins (1-6) on the release of b-hexosaminidase from RBL-2H3 cells. In this paper, we describe the isolation and structure elucidation of the new constituents (4-9) and the inhibitory effect of major floratheasaponins (1-6) from the flower buds of Chinese C. sinensis on the release of b-hexosaminidase from RBL-2H3 cells.14)The methanolic extract (38.5% from the dried flower buds of C. sinensis cultivated in Anhui province of China) with the inhibitory effect on the release of b-hexosaminidase from