Su Hyun Kim
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Su Hyun Kim has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Hee Jae Shin
Marine Natural Products Chemistry Laboratory, Korea Institute of Ocean Science and Technology, 385 Haeyang-ro, Yeongdo-gu, Busan 49111, Republic of Korea
1 shared publication - Hyi-Seung Lee
Marine Natural Products Chemistry Laboratory, Korea Institute of Ocean Science and Technology, Busan, 49111, Republic of Korea
1 shared publication - Jihoon Lee
Korea Institute of Ocean Science & Technology (KIOST), Busan 49111, Republic of Korea
1 shared publication - Jong Seok Lee
Korea Institute of Ocean Science & Technology
1 shared publication - Saem Han
Marine Nautral Product Chemistry Laboratory, Korea Institute of Ocean Science and Technology, Ansan 15627, Korea
1 shared publication - Yeon-Ju Lee
Korea Institute of Ocean Science and Technology
1 shared publication
Latest Publications
- Open Access
- 4 December 2017
- Published by MDPI AG in Marine Drugs
- Vol. 15 (12) , 379
Three New Cytotoxic Steroidal Glycosides Isolated from Conus pulicarius Collected in Kosrae, Micronesia
Three new sulfated steroidal glycosides (3–5), along with known cholesterol derivatives (1,2), were isolated from the visceral extract of the cone snail Conus pulicarius. The structure of each new compound was elucidated by nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. The three new compounds exhibited significant in vitro cytotoxicity (GI50 values down to 0.49 μM) against the K562 human leukemia cell line.
- 4 December 2017
- Published by MDPI AG in Marine Drugs
- Vol. 15 (12) , 379
Open AccessThree New Cytotoxic Steroidal Glycosides Isolated from Conus pulicarius Collected in Kosrae, Micronesia
Three new sulfated steroidal glycosides (3–5), along with known cholesterol derivatives (1,2), were isolated from the visceral extract of the cone snail Conus pulicarius. The structure of each new compound was elucidated by nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. The three new compounds exhibited significant in vitro cytotoxicity (GI50 values down to 0.49 μM) against the K562 human leukemia cell line.