| Literature DB >> 27983842 |
Yulin Ren, Wei-Lun Chen1, Daniel D Lantvit1, Ellen J Sass, Pratik Shriwas, Tran Ngoc Ninh2, Hee-Byung Chai, Xiaoli Zhang, Djaja D Soejarto1,3, Xiaozhuo Chen, David M Lucas, Steven M Swanson1,4, Joanna E Burdette1, A Douglas Kinghorn.
Abstract
Three new (1-3) and two known (4 and 5) cytotoxic cardiac glycosides were isolated and characterized from a medicinal plant, Streblus asper Lour. (Moraceae), collected in Vietnam, with six new analogues and one known derivative (5a-g) synthesized from (+)-strebloside (5). A preliminary structure-activity relationship study indicated that the C-10 formyl and C-5 and C-14 hydroxy groups and C-3 sugar unit play important roles in the mediation of the cytotoxicity of (+)-strebloside (5) against HT-29 human colon cancer cells. When evaluated in NCr nu/nu mice implanted intraperitoneally with hollow fibers facilitated with either MDA-MB-231 human breast or OVCAR3 human ovarian cancer cells, (+)-strebloside (5) showed significant cell growth inhibitory activity in both cases, in the dose range 5-30 mg/kg.Entities:
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Year: 2016 PMID: 27983842 PMCID: PMC5365359 DOI: 10.1021/acs.jnatprod.6b00924
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050