1346653-48-2Relevant academic research and scientific papers
Diastereoselective synthesis and bioactivity of long-chain anti-2-amino-3-alkanols
Chen, Bi-Shuang,Yang, Long-He,Ye, Jian-Liang,Huang, Tao,Ruan, Yuan-Ping,Fu, Jin,Huang, Pei-Qiang
, p. 5480 - 5486 (2011/12/14)
An improved four-step approach for the stereoselective synthesis of long-chain anti-2-amino-3-alkanols is described. Using this method, the syntheses of antiproliferative (antitumoral) compounds, spisulosine (ES-285, 2), clavaminols A and B (3 and 4), the deacetylated products of clavaminols H and N (7 and 8), as well as (2S,3R)-2-aminododecan-3-ol (9) and xestoaminol C (10), have been achieved in excellent diastereoselectivities. In vitro study showed that these compounds induced cell death and dose-dependently inhibited cell proliferation in human glioblastoma cell line SHG-44, indicating the anti-tumor property of this series of compounds.
