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Correction: Synthesis and biological evaluation of hybrids from farnesylthiosalicylic acid and hydroxylcinnamic acid with dual inhibitory activities of Ras-related signaling and phosphorylated NF-κB

Yong Ling ab, Zhiqiang Wang ab, Xuemin Wang a, Ying Zhao a, Wei Zhang a, Xinyang Wang a, Li Chen bc, Zhangjian Huang *bc and Yihua Zhang *bc
aSchool of Pharmacy, Nantong University, Nantong, 226001, PR China
bState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, 210009, PR China. E-mail: zyhtgd@163.com; cpudahuang@163.com; Fax: +86-25-83271015; Tel: +86-25-83271015
cCenter of Drug Discovery, China Pharmaceutical University, Nanjing, 210009, PR China

Received 10th December 2020 , Accepted 10th December 2020

First published on 4th January 2021


Abstract

Correction for ‘Synthesis and biological evaluation of hybrids from farnesylthiosalicylic acid and hydroxylcinnamic acid with dual inhibitory activities of Ras-related signaling and phosphorylated NF-κB’ by Yong Ling et al., Org. Biomol. Chem., 2014, 12, 4517–4530, DOI: 10.1039/C4OB00023D.


The authors regret that there was an incorrect western blot image shown in Fig. 6A representing the Akt group. The correct Fig. 6 is shown below.
image file: d0ob90173c-f6.tif
Fig. 6 Immunoblot analysis of the expression and phosphorylation of the Ras-related signal events in vitro. (A) SMMC-7721 cells were treated with the vehicle (control), different doses of 5f or FTS were homogenized, and their lysates were subjected to immunoblot analysis using antiphospho-Raf (Ser259), antiphospho-ERK1/2 (Thr202/Tyr204), anti-Akt, antiphospho-Akt (Ser473), anti-phoshpo-NF-κB p65, anti-NF-κB and anti-β-actin antibodies, respectively. β-Actin was used as the control. (B) Quantitative analysis. The relative levels of each signaling event to the control β-actin were determined by densimetric scanning. The data are expressed as means ± SD from three duplicate experiments. *P < 0.01 vs. the control.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.


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