Two new tridesmosidic glycosides of (3b,6a,16b,20R,24S)-20,24-epoxycycloartane-3,6,16,25-tetrol (¼ cycloastragenol), armatosides I and II (1 and 2, resp.), were isolated from the roots of Astragalus armatus (Fabaceae) as well as the known bidesmosidic glycosides of cycloastragenol, trigonoside II (3) and trojanoside H (4). Their structures were elucidated as (3b,6a,16b,20R,24S) -3,6,16,25-tetrol (1), and (3b,6a,16b,20R,24S) 6,16,25-tetrol (2). These structures were established by extensive NMR and MS analyses and by comparison with literature data.Introduction. -Astragalus is a great legume genus including more than 2200 species growing worldwide [1]. Saponins with aglycones of the cycloartane-, lanostane-and oleanane-type were isolated from many Astragalus species, but the cycloartane glycosides dominate the triterpenoids of this genus [2] [3] (cycloartane ¼ 9,19-cyclolanostane). Among the cycloartane-type skeletons, cycloastragenol (also known as cyclosiversigenin and astramembrangenin) is the most widely distributed genin of the glycosides in Astragalus genus [2]. The identified saponins were found to be diversified by their glycosylation types, degrees, and attachment points at the genin; moreover, several of them were acetylated. These different structural characteristics lead to specific chemical traits which could be used as fingerprints to distinguish different Astragalus species from each other. Astragalus armatus Willd. (Fabaceae) is an endemic shrub species in the region of Maghreb. It mainly grows in arid regions where pastoral activity is important because of its low palatability [4] [5]. To the best of our knowledge, there are no phytochemical studies on this species to date. In this article, we describe the isolation and structural elucidation of two new acylated tridesmosides of a 20,24-epoxycycloartane-type aglycone from the roots of A. armatus, named armatosides I (1) and II (2), together with two known cycloartane-type glycosides, trigonoside II (3) [6] and trojanoside H (4) [7]. The new compounds showed unique chemical substitutions which are not frequently found in the genus Astragalus.