Preparation and Activity of β-Substituted Acetylcholine Iodides
作者:George H. Cocolas、Ellen C. Robinson、William L. Dewey、Theodore C. Spaulding
DOI:10.1002/jps.2600601144
日期:1971.11
enantiometers of (—)- and (+)-acetyl β-ethylcholine iodide were prepared following the resolution of 1-dimethylamino-2-butanol from (+)-tartaric acid and (+)-bromocamphor-sulfonic acid for the (—)- and (+)-isomers, respectively. The absoluteconfiguration of the (—)-enantiomer was determined by the synthesis of (—)-acetyl β-ethylcholine iodide from R(—)-2-hydroxybutyric acid. The opticallyactive acetyl β-phenylcholine
[EN] PROCESSES FOR PREPARATION OF IDELALISIB AND INTERMEDIATES THEREOF<br/>[FR] PROCÉDÉS DE PRÉPARATION D'IDÉLALISIB ET DE SES INTERMÉDIAIRES
申请人:DR REDDY’S LABORATORIES LTD
公开号:WO2016108206A3
公开(公告)日:2016-08-18
New diterpene pyrone-type compounds, metarhizins A and B, isolated from entomopathogenic fungus, Metarhizium flavoviride and their inhibitory effects on cellular proliferation
To date, entomopathogenic fungi have not been extensively examined by natural product chemists. In this study, we isolated novel pyrone diterpene-type compounds, metarhizins A (1) and B (2), from methanol extracts of entomopathogenic fungus, Metarhizium flavoviride. They showed potent and selective antiproliferative activity against both insect and human cancer cell lines. These results indicate that metarhizins A (1) and B (2) can be used as novel lead compounds for anti-cancer agents and probes for cell cycle regulation. To further investigate the structural requirements for this inhibitory activity, we synthesized many metarhizin derivatives and evaluated their antiproliferative activities. (C) 2008 Elsevier Ltd. All rights reserved.
EP0168480A4
申请人:——
公开号:EP0168480A4
公开(公告)日:1987-10-08
PROCESS FOR PREPARING OPTICALLY-ACTIVE 4-AMINO-3-HYDROXYBUTYRIC ACID