Synthesis and biological activities of flavolipids
摘要:
Syntheses of the bacterial surfactants 6S 6S- 9S 9S- and 9U 9U-flavolipids confirmed the structures proposed for them from spectroscopic analysis of a flavolipid mixture and made pure flavolipids available for the first time All three synthetic flavolipids and a straight chain analogue were found to be weakly cytotoxic and to inhibit metastatic cancer cell migration with 9U 9U-fiavolipid (the most abundant natural flavolipid) having the most activity Biosynthetic routes to the branched side-chains of the flavolipids are suggested and it is proposed that branched chains are employed to hinder biodegradation (C) 2010 Elsevier Ltd All rights reserved
[EN] HYDROCAPSULES AND METHOD OF PREPARATION<br/>[FR] HYDROCAPSULES ET LEUR PROCEDE DE PREPARATION
申请人:ANALYTICAL RES SYSTEMS
公开号:WO2003059503A1
公开(公告)日:2003-07-24
A method is described for the formation of microcapsules which contain a liquid composition in the core, which is surrounded by a polymeric shell, membrane, or coating. The microcapsules are produced by simultaneously extruding the liquid core material along with a polymerizable liquid through concentrically-aligned nozzles to form spherically-layered biliqued droplets, followed by energy input in the form of heat or light which causes polymerization of the outer layer. The capsules formed by this method are capable of containing a variety of liquid materials having a composit ion ranging from completely aqueous to completely non-aqueous.
Characterization of FabG and FabI of the<i>Streptomyces coelicolor</i>Dissociated Fatty Acid Synthase
作者:Renu Singh、Kevin A. Reynolds
DOI:10.1002/cbic.201402670
日期:2015.3.2
Functional crosstalk: β‐Ketoacyl‐acyl carrier protein (ACP; FabG) and enoyl‐ACP reductase (FabI) from Streptomyces coelicolor were identified and characterized. Kinetic analysis demonstrated that these enzymes process straight and branched‐chain substrates along with the ACPs from both fattyacid and undecylprodiginine biosynthetic pathways. This relaxed substrate specificity allow these enzymes to
Synthesis and biological activities of flavolipids
作者:Samiul M. Ahad、Alison L. Ange、Robert B. Bates、Bonnie L. Bell、Adria A. Bodour、Bryan R. Bourne、Cristina G. Contreras、Emily L. Goldberg、A.A. Leslie Gunatilaka、Sheryl King、Albert K. Lee、Rebecca L. Low、Raina M. Maier、Kathryn M. Marlor、Marilyn T. Marron、Ryan C. Scolnik、Matthew J. Streeter、Malgorzata Strelczuk、Long N. Trinh、Vu K. Truong、Sage P. Vissering、Megan C. Weick、Maria T. Williams
DOI:10.1016/j.tet.2010.09.088
日期:2010.11
Syntheses of the bacterial surfactants 6S 6S- 9S 9S- and 9U 9U-flavolipids confirmed the structures proposed for them from spectroscopic analysis of a flavolipid mixture and made pure flavolipids available for the first time All three synthetic flavolipids and a straight chain analogue were found to be weakly cytotoxic and to inhibit metastatic cancer cell migration with 9U 9U-fiavolipid (the most abundant natural flavolipid) having the most activity Biosynthetic routes to the branched side-chains of the flavolipids are suggested and it is proposed that branched chains are employed to hinder biodegradation (C) 2010 Elsevier Ltd All rights reserved