| Literature DB >> 26001122 |
Bui Thi Ngoan1, Tran Thi Hong Hanh1, Le Thi Vien1, Chau Ngoc Diep1, Nguyen Phuong Thao1, Do Thi Thao2, Nguyen Van Thanh1, Nguyen Xuan Cuong1, Nguyen Hoai Nam1, Do Cong Thung3, Phan Van Kiem1, Young Ho Kim4, Chau Van Minh1.
Abstract
Using combined chromatographic methods, two asterosaponins (compounds 1 and 2), including a new compound novaeguinoside E (compound 1), and six glycosylated polyhydroxysteroids (compounds 3-8) were isolated from a methanol extract of the starfish Culcita novaeguineae. Their structures were determined on the basis of spectroscopic data ((1)H and (13)C NMR, HSQC, HMBC, (1)H-(1)H COSY, ROESY, and HRESI-MS) and by comparison with the literature values. The new compound 1 represents the third example of asterosaponins containing the 5α-cholesta-9(1l)-en-3β,6α,20,22-tetraol aglycone. Among isolated compounds, 4-7 exhibited moderate to weak cytotoxic activities against five human cancer cell lines such as Hep-G2 (hepatoma), KB (epidermoid carcinoma), LNCaP (prostate cancer), MCF7 (breast cancer), and SK-Mel2 (melanoma).Entities:
Keywords: Culcita novaeguineae; Oreasteridae; cytotoxic activity; novaeguinoside E; starfish
Mesh:
Substances:
Year: 2015 PMID: 26001122 DOI: 10.1080/10286020.2015.1041930
Source DB: PubMed Journal: J Asian Nat Prod Res ISSN: 1028-6020 Impact factor: 1.569