Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 2020 Jan 22;177(1):235. doi: 10.1111/bph.14944

CORRECTION

PMCID: PMC6976875  PMID: 31970763

The authors of Murillo‐Carretero et al. (2017) have supplied the following correction to their article.

There is an error that affects the structure of one of the non‐active products described in the article, the so‐called EOF2, which we described as 7,8,12‐tri‐O‐acetyl‐3‐O‐(4‐methoxyphenyl)acetylingol (CAS number: 944799‐47‐7). Chemical transformations on the compound used for the work led us to conclude that the compound described as EOF2 is actually 3,8,12‐tri‐O‐acetyl‐7‐O‐(4‐methoxyphenyl)acetylingol (CAS number: 2230806‐06‐9). This error does not affect the results and conclusions presented in the article.

The corrected structure from Figure 1 is shown below.

chemical structure image

The authors apologize for the errors and any inconvenience it may have caused.

CORRECTION. Br J Pharmacol. 2020;177:235–235. 10.1111/bph.14944

REFERENCE

  1. Murillo‐Carretero, M. , Geribaldi‐Doldán, N. , Flores‐Giubi, E. , García‐Bernal, F. , Navarro‐Quiroz, E. A. , Carrasco, M. , … Castro, C. (2017). ELAC (3,12‐di‐O‐acetyl‐8‐O‐tigloilingol), a plant‐derived lathyrane diterpene, induces subventricular zone neural progenitor cell proliferation through PKCβ activation. British Journal of Pharmacology, 174(14), 2373–2392. 10.1111/bph.13846 [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES