Synthesis of indomethacin analogues for evaluation as modulators of MRP activity

被引：43

作者：

Maguire, AR ^{[1
]}

Plunkett, SJ

Papot, S

Clynes, M

O'Connor, R

Touhey, S

机构：

[1] Natl Univ Ireland Univ Coll Cork, Dept Chem, Cork, Ireland

[2] Dublin City Univ, Natl Cell & Tissue Culture Ctr, Dublin 9, Ireland

来源：

BIOORGANIC & MEDICINAL CHEMISTRY | 2001年 / 9卷 / 03期

关键词：

D O I：

10.1016/S0968-0896(00)00292-3

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Synthesis of a range of indomethacin analogues, required for investigation in combination toxicity assays, bearing both N-benzyl and N-benzoyl groups, is described. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：745 / 762

页数：18

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