Four triterpenoids named (9b,31R)-9,25-cyclo-30-propylhopan-31-ol (1), (3b)-3-hydroxy-30-propylhopan-31-one (2), (3b)-oleanan-3-ol (3), and (3b,9b)-9,25-cycloolean-12-en-3-yl b-d-glucofuranoside (4), a steroid named (3b,9b,14b)-14-hydroxy-9,19-cyclocholan-3-yl b-d-glucopyranoside (5), and an anthraquinone named 6-hydroxy-5,7,8-trimethoxy-9,10-dioxo-9,10-dihydroanthracen-2-yl acetate (6) have been isolated from the fruits and bark of Celtis australis (Ulmaceae), along with apigenin, quercetin, and its glucoside. Their structures were elucidated by means of chemical and spectral analysis including COSY, NOESY, and HMBC experiments.Introduction. -Celtis australis L. of Ulmaceae is a deciduous tree distributed from montane to submontane Himalaya. The plant has been used as remedy for bone fracture, pimples, contusions, sprains, and joints pain in the traditional Indian medicine [1]. Previous studies on the plants of the genus Celtis led to the isolation of phenolic glycosides [2], steroids [3], terpenoids [4] [5], and tannins, saponins, and alkaloids [6]. From the leaves of C. australis, three phenol derivatives, acacetin 7-O-glucoside, isovitexin, and cytisoside were reported [7]. Recently, we have isolated a novel sulfonated phenolic celtisanin from the fruits [8] and a bacteriohopanoid, (3b)-33-ethyl-3-hydroxy-34-methyl-35-(3-propanoylcyclohex-1-yl)bacteriohopane from the stem bark [9] of this plant. Here, we describe the isolation and structure elucidation of four triterpenoids, 1 -4, one steroid, 5, and one anthraquinone, 6, for the first time from this source.