Synthesis and in vivo biological activity of large-ringed calixarenes against Mycobacterium tuberculosis

被引:21
|
作者
Goodworth, Kerry J. [1 ]
Herve, Anne-Cecile [1 ]
Stavropoulos, Evangelos [2 ]
Herve, Gwenaelle [1 ]
Casades, Isabel [1 ,2 ]
Hill, Alison M. [3 ]
Weingarten, Gordon G. [4 ]
Tascon, Ricardo E. [2 ]
Colston, M. Joseph [2 ]
Hailes, Helen C. [1 ]
机构
[1] UCL, Dept Chem, London WC1H 0AJ, England
[2] Natl Inst Med Res, London NW7 1AA, England
[3] Univ Exeter, Hatherly Labs, Sch Biosci, Exeter EX4 4PS, Devon, England
[4] GlaxoSmithKline Inc, Med Res Ctr, Stevenage SG1 2NY, Herts, England
基金
英国生物技术与生命科学研究理事会;
关键词
Calixarenes; Tuberculosis; Anti-mycobacterial; p-Phenylcalixarene; Calixarene alkylation; Pegylation; POLYOXYETHYLENE ETHERS; TRANSFECTION; CONFORMATION; MACROPHAGES;
D O I
10.1016/j.tet.2010.11.034
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of large-ringed calix[6,7,8]arene analogues have been synthesised and their affect against Mycobacterium tuberculosis in vivo established. In general, when p-phenylcalixarenes and tert-butylcalixarenes were not functionalised at the lower rim, low biological activities were observed. However on going from partially to fully lower rim pegylated calixarenes the anti-mycobacterial properties improved. The addition of cyanopropoxy groups at the lower rim gave rise to low activities, whereas the addition of acetate moieties interestingly had pro-TB effects. Two upper rim sulfonated calixarenes showed promising properties. In the course of this work, a high yielding procedure to synthesise p-phenylcalix[7]arene was also established. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:373 / 382
页数:10
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