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Quan-Hoang Vuong,Viet-Phuong La,Manh-Tung Ho,Thu-Trang Vuong,Manh-Toan Ho 한국과학학술지편집인협의회 2020 Science Editing Vol.7 No.1
Purpose: Although retractions are commonly considered to be negative, the fact remains that they play a positive role in the academic community. For instance, retractions help scientific enterprise perform its self-correcting function and provide lessons for future researchers; furthermore, they represent the fulfillment of social responsibilities, and they enable scientific communities to offer better monitoring services to keep problematic studies in check. This study aims to provide a thorough overview of the practice of retraction in scientific publishing from the first incident to the present. Methods: We built a database using SQL Server 2016 and homemade artificial intelligence tools to extract and classify data sources including RetractionWatch, official publishers’ archives, and online communities into ready-to-analyze groups and to scan them for new data. After data cleaning, a dataset of 18,603 retractions from 1,753 (when the first retracted paper was published) to February 2019, covering 127 research fields, was established. Results: Notable retraction events include the rise in retracted articles starting in 1999 and the unusual number of retractions in 2010. The Institute of Electrical and Electronics Engineers, Elsevier, and Springer account for nearly 60% of all retracted papers globally, with Institute of Electrical and Electronics Engineers contributing the most retractions, even though it is not the organization that publishes the most journals. Finally, reasons for retraction are diverse but the most common is “fake peer review”. Conclusion: This study suggests that the frequency of retraction has boomed in the past 20 years, and it underscores the importance of understanding and learning from the practice of retracting scientific articles.
Compounds from the Seeds of Myristica fragrans and Their Cytotoxic Activity
TODAO CUONG,Chae Jin Lim,Tran Thi Thu Trang,Yoon Ho Bae,NGUYENVAN THU,Nguyen The Tung,Tran Manh Hung,우미희,최재수,민병선 한국생약학회 2012 Natural Product Sciences Vol.18 No.2
Six lignan compounds, 1-(17,21-dihydroxyphenyl)-9-(12,13-dihydroxyphenyl)-1-nonanone (malabaricone C) (1), 7'-(3',4'-methylenedioxyphenyl)-8,8'-dimethyl-7-(3,4-dihydroxyphenyl)-butane (2), 7'-(3',4'-dimethoxyphenyl)-8,8'-dimethyl-7-(3-methoxy-4-hydroxyphenyl)-butane (3), 7-(4-hydroxy-3-methoxyphenyl)-7′-(3′,4′-methylenedioxyphenyl)-8,8′-lignan-7-methyl ether (4), (+)-erythro-(7S,8R)-Δ8′-7-hydroxy-3,4,3′,5′-tetramethoxy-8-O-4′-neolignan (5), and (+)-erythro-(7S,8R)-Δ8′-7-acetoxy-3,4,3′,5′-tetramethoxy-8-O-4′-neolignan (6), were isolated from the seeds of Myristica fragrans. The chemical structures of these compounds were determined on the basis of spectroscopic analyses including 2D NMR. Compounds 1 - 6 were evaluated for their cytotoxic activity against the HL-60, MCF-7, and A549 cancer cell lines in in vitro.
Tai, Bui Huu,Jung, Bong Yong,Cuong, Nguyen Manh,Linh, Pham Thuy,Tung, Nguyen Huu,Nhiem, Nguyen Xuan,Huong, Tran Thu,Anh, Ngo Thi,Kim, Jeong Ah,Kim, Sang Kyum,Kim, Young Ho Pharmaceutical Society of Japan 2009 Biological & pharmaceutical bulletin Vol.32 No.12
<P>Nine compounds, including six phenylethanoid glycosides: acteoside (1); bioside (2); echinacoside (3); poliumoside (4); phenylethyl glycoside (5); salidroside (6) and three flavonoids; linarin (7); apigenin (8); isorhoifolin (9), were isolated from the flowers of <I>Buddleja officinalis</I> M<SMALL>AXIM</SMALL>. (Buddlejaceae). Chemical structures were confirmed by <SUP>1</SUP>H-, and <SUP>13</SUP>C-NMR, and MS spectral methods and compared with those reported in the literature. Antioxidant activities of the methanol and water extracts, and all isolated compounds were evaluated using the total oxidant scavenging capacity (TOSC) assay against peroxynitrite. Results of the assay showed that the phenylethanoid glycosides, a major class of compounds of the flowers of <I>B. officinalis</I>, possess strong antioxidant activity. Of these, acteoside, echinacoside and poliumoside have 9.9-, 9.8- and 9.5-fold TOSC value, respectively, compared with the positive control, Trolox.</P>