Cynanchum viminale subsp. australe, more commonly known as caustic vine, is a leafless succulent that grows in the northern arid zone of Australia. Toxicity toward livestock has been reported for this species, along with use in traditional medicine and its potential anticancer activity. Disclosed herein are novel seco-pregnane aglycones cynavimigenin A (5) and cynaviminoside A ( 6), together with new pregnane glycosides cynaviminoside B (7) and cynavimigenin B (8). Cynavimigenin B (8) contains an unprecedented 7-oxobicyclo[2.2.1]heptane moiety in the seco-pregnane series, likely arising from a pinacol-type rearrangement. Interestingly, these isolates displayed only limited cytotoxicity in cancer and normal human cell lines, in addition to low activity against acetylcholinesterase and Sarcoptes scabiei bioassays, suggesting that 5−8 are not associated with the reported toxicity of this plant species.Cynanchum is a large genus of plants belonging to the Apocynaceae family (milkweed family, formerly Sarcostemma 1,2 ), consisting of over 200 species distributed worldwide. 3 Cynanchum species have long been used in Asia as traditional medicine for the treatment of common and chronic diseases. 3 Australia is home to around 13 native species of Cynanchum, occurring most commonly in northern Australia, 1,2,4 and certain species, in particular C. viminale subsp. australe (R.Br.) Mere & Liede, are known to have been used by Aboriginal peoples for the treatment of several conditions, including the topical treatment of wounds, cuts, and sores. 5 In addition, crude extracts of C. viminale subsp. australe have been reported to display cancer cell line cytotoxicity activity 6 and are especially active against skin cancer. 7 Interestingly, C. viminale subsp. australe has been reported to display toxicity toward livestock to varying extents all depending on location and/or drought, 8 which is also the case for a closely related Australian species, C. brevipedicellatum. 1 Livestock toxicity has also been observed in South Africa arising from other Cynanchum species and subspecies of C. viminale and was attributed to an abundance of pregnane glycosides 9,10 in the plant latex, such as sarcovimisides A−C (1−3) from C. viminale 11 and cynafoside A (4) from C. af ricanum 12 (Figure 1). Structurally, pregnane glycosides consist of a C 21 pregnane aglycone with a hydroxy group at C-3 and a substituent at C-17 and typically also contain an additional O-linked substituent at C-12. 9,10 The glycoside unit is typically comprised of a linear chain of mixed sugars, commonly glucose, rhamnose, and dideoxy sugars such as oleandrose, cymarose, or digitoxose. 9,10 While the most common aglycone motif within this family is 14β-hydroxypregnane, an increasing number of 14,15-and 8,14-seco-pregnane aglycones have been reported, along with a wider range of pharmacological effects. 13 Considering that very early attempts were unable to fully elucidate saponins from C. viminale subsp. australe, 14 and the Cynanchum genus aligns with our continued effort...