Su-Ying Chien

Dr. Su-Ying Chien

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Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 February 2021 in Marine Drugs
Verified
Journal Article
Open access
PDF file
THThanh-Hao Huynh
Thanh-Hao Huynh
SCSu-Ying Chien
Su-Ying Chien
JTJunichi Tanaka
Junichi Tanaka
ZWZhi-Hong Wen
Zhi-Hong Wen
Yang-Chang WuYang-Chang Wu
Yang-Chang Wu
Ping-Jyun SungPing-Jyun Sung
Ping-Jyun Sung
Chemical investigation of the octocoral Briareum stechei, collected in the Ie Island, Okinawa, Japan, resulted in the isolation of a new briarane-type diterpenoid, briastecholide A (1), as well as the previously reported metabolites, solenolide C (2) and briarenolide S (3). The structures of briaranes 1–3 were characterized through spectroscopic analysis, and the absolute configuration of 2 was corroborated by a single-crystal X-ray diffraction analysis. Briarane 3 exhibited bioactivity against the protein expression of inducible nitric oxide synthase (iNOS).

14 February 2023 in Marine Drugs
Verified
Journal Article
Open access
PDF file
THThanh-Hao Huynh
Thanh-Hao Huynh
CLChia-Jung Liu
Chia-Jung Liu
YLYi-Hung Liu
Yi-Hung Liu
SCSu-Ying Chien
Su-Ying Chien
ZWZhi-Hong Wen
Zhi-Hong Wen
Ping-Jyun SungPing-Jyun Sung
Ping-Jyun Sung
The chemical screening of a cultured soft coral, Briareum violaceum, led to the isolation of eight natural, briarane-related diterpenoids, including three unreported metabolites, briavioids E–G (1–3), and five known briaranes, briacavatolides B (4) and C (5), briaexcavatin L (6), briaexcavatolide U (7) and briarenol K (8). The structures of briaranes 1–8 were established using spectroscopic methods. The absolute configuration of briavioid A (9), obtained in a previous study, was reported for the first time in this study by a single-crystal X-ray diffraction analysis using a copper radiation source. The anti-inflammatory activity of briaranes 1 and 2 and briaranes 4–8 was evaluated by screening their inhibitory ability against the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) proteins in lipopolysaccharide (LPS)-induced RAW 264.7 macrophage cells.