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Correction: Design, synthesis, and evaluation of semi-conservative mono-carbonyl analogs of curcumin as anti-inflammatory agents against lipopolysaccharide-induced acute lung injury
Lili
Dong
ab,
Suqing
Zheng
a,
Yali
Zhang
a,
Xin
Jiang
c,
Jianzhang
Wu
a,
Xiaoqin
Zhang
d,
Xiaoou
Shan
b,
Dandan
Liang
a,
Shilong
Ying
a,
Jianpeng
Feng
*a and
Guang
Liang
*a
aChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China. E-mail: chemime@163.com; Fax: +86 577 86699527; Tel: +86 577 86699524
bThe 2nd Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China
cThe Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310003, China
dSchool of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China
First published on 7th August 2015
Abstract
Correction for ‘Design, synthesis, and evaluation of semi-conservative mono-carbonyl analogs of curcumin as anti-inflammatory agents against lipopolysaccharide-induced acute lung injury’ by Lili Dong et al., Med. Chem. Commun., 2015, 6, 1544.
The authors regret the following errors in Fig. 1.
For 1: R = 3-indolyl should be changed to R = 1H-indol-2-yl.
For 3: R = 3-pyrrolopyrimidine should be changed to R = 1H-pyrrolo[2,3-b]pyridin-3-yl.
For 5 and 16: R = 6-bromo-1,3-dihydroisobenzofuran-5-yl should be changed to R = 6-bromobenzo[d][1,3]dioxol-5-yl.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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