Jong Eel Park
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Jong Eel Park has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Kang Ro Lee
Natural Products Laboratory, School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea
3 shared publications Je Hyun Lee
Department of Korean Medicine, Dongguk University, Gyeongju-si, Gyeongbuk 780-714, Korea
2 shared publicationsKyeong Wan Woo
Natural Products Laboratory, School of Pharmacy, Sungkyunkwan University, Suwon 440-746, Korea, (phone: +82-31-2907710; fax: +82-31-2907730)
2 shared publications- Chung Sub Kim
Sungkyunkwan University
1 shared publication - Lalita Subedi
College of Pharmacy and Gachon Institute of Pharmaceutical Sciences, Gachon University, Incheon 21936, Republic of Korea
1 shared publication Sang Un Choi
Korea Research Institute of Chemical Technology, Teajeon 305-600, Korea
1 shared publication
Latest Publications
- Open Access
- 28 February 2022
- Published by MDPI AG in Antioxidants
- Vol. 11 (3) , 482
Anticancer and Anti-Neuroinflammatory Constituents Isolated from the Roots of Wasabia japonica
Wasabi (Wasabia japonica (Miq.) Matsum.) is a pungent spice commonly consumed with sushi and sashimi. From the roots of this plant, a new 2-butenolide derivative (1) and 17 previously reported compounds (2–18) were isolated and structurally characterized. Their chemical structures were characterized based on the conventional NMR (1H and 13C, COSY, HSQC, and HMBC) and HRESIMS data analysis. All of these phytochemicals (1–18) were evaluated for their antiproliferative effects on the four human tumor cell lines (A549, SK-OV-3, SK-MEL-2, and MKN-1), for their inhibitory activity on nitric oxide (NO) production in lipopolysaccharide (LPS)-activated BV-2 microglia cells, and for their nerve growth factor (NGF)-releasing effect from C6 glioma cells. Among the isolated compounds, compound 15 showed powerful antiproliferative activities against A549 and SK-MEL-2 cell lines with IC50 values of 2.10 and 9.08 μM, respectively. Moreover, the new compound 1 exhibited moderate NO inhibition activity with IC50 value of 45.3 μM.
- 28 February 2022
- Published by MDPI AG in Antioxidants
- Vol. 11 (3) , 482
Open AccessAnticancer and Anti-Neuroinflammatory Constituents Isolated from the Roots of Wasabia japonica
Wasabi (Wasabia japonica (Miq.) Matsum.) is a pungent spice commonly consumed with sushi and sashimi. From the roots of this plant, a new 2-butenolide derivative (1) and 17 previously reported compounds (2–18) were isolated and structurally characterized. Their chemical structures were characterized based on the conventional NMR (1H and 13C, COSY, HSQC, and HMBC) and HRESIMS data analysis. All of these phytochemicals (1–18) were evaluated for their antiproliferative effects on the four human tumor cell lines (A549, SK-OV-3, SK-MEL-2, and MKN-1), for their inhibitory activity on nitric oxide (NO) production in lipopolysaccharide (LPS)-activated BV-2 microglia cells, and for their nerve growth factor (NGF)-releasing effect from C6 glioma cells. Among the isolated compounds, compound 15 showed powerful antiproliferative activities against A549 and SK-MEL-2 cell lines with IC50 values of 2.10 and 9.08 μM, respectively. Moreover, the new compound 1 exhibited moderate NO inhibition activity with IC50 value of 45.3 μM.
- 17 January 2014
- Published by Wiley in Helvetica Chimica Acta
- Vol. 97 (1) , 56-63
Two New Cytotoxic Spirostane‐Steroidal Saponins from the Roots of Bletilla striata
Two new spirostane‐steroidal saponins, bletilnoside A (1) and bletilnoside B (2), together with five known compounds, 3–7, were isolated from the roots of Bletilla striata (Thunb.) Reichb. F. The structures of the new compounds were determined based on their 1D‐ and 2D‐NMR spectral data. The isolated compounds 1–7 were tested for cytotoxicity against four human tumor cells (A549, SK‐OV‐3, SK‐MEL‐2, and HCT15) in vitro using a sulforhodamin B bioassay, and compounds 1, 2, and 5 showed significant cytotoxicities against all tested tumor cell lines with IC50 values ranging from 3.98±0.16 to 12.10±0.40 μM.
- 17 January 2014
- Published by Wiley in Helvetica Chimica Acta
- Vol. 97 (1) , 56-63
Two New Cytotoxic Spirostane‐Steroidal Saponins from the Roots of Bletilla striata
Two new spirostane‐steroidal saponins, bletilnoside A (1) and bletilnoside B (2), together with five known compounds, 3–7, were isolated from the roots of Bletilla striata (Thunb.) Reichb. F. The structures of the new compounds were determined based on their 1D‐ and 2D‐NMR spectral data. The isolated compounds 1–7 were tested for cytotoxicity against four human tumor cells (A549, SK‐OV‐3, SK‐MEL‐2, and HCT15) in vitro using a sulforhodamin B bioassay, and compounds 1, 2, and 5 showed significant cytotoxicities against all tested tumor cell lines with IC50 values ranging from 3.98±0.16 to 12.10±0.40 μM.
- 20 May 2013
- Published by Korean Chemical Society in Bulletin of the Korean Chemical Society
- Vol. 34 (5) , 1589-1591
Two New ent-Kaurane Diterpenoids from the Roots of Fritillaria thunbergii
- 20 May 2013
- Published by Korean Chemical Society in Bulletin of the Korean Chemical Society
- Vol. 34 (5) , 1589-1591
Two New ent-Kaurane Diterpenoids from the Roots of Fritillaria thunbergii