Jae Sang Han

Dr. Jae Sang Han

orcid

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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30 November 2021 in Molecules
Verified
Journal Article
Open access
PDF file
JLJin Woo Lee
Jin Woo Lee
JKJun Gu Kim
Jun Gu Kim
JHJae Sang Han
Jae Sang Han
YCYong Beom Cho
Yong Beom Cho
YLYu Jin Lee
Yu Jin Lee
Bang Yeon HwangBang Yeon Hwang
Bang Yeon Hwang
Orbitides are plant-derived small cyclic peptides with a wide range of biological activities. Phytochemical investigation of the whole plants of Dianthus chinensis was performed with the aim to discover new bioactive orbitides. Five undescribed proline-containing orbitides, dianthiamides A–E (1–5), were isolated from a methanolic extract of Dianthus chinensis. Their structures were elucidated by extensive analysis of 1D and 2D NMR and HRESI–TOF–MS as well as ESI–MS/MS fragmentation data. The absolute configuration of the amino acid residues of compounds 1–5 was determined by Marfey’s method. All compounds were tested for their cytotoxic activity, and dianthiamide A (1) exhibited weak activity against A549 cell line with IC50 value of 47.9 μM.

22 October 2024 in Phytochemistry
Verified
Journal Article
Closed access
JKJun Gu Kim
Jun Gu Kim
JHJae Sang Han
Jae Sang Han
YCYong Beom Cho
Yong Beom Cho
BABeom Kyun An
Beom Kyun An
DLDongho Lee
Dongho Lee
Bang Yeon HwangBang Yeon Hwang
Bang Yeon Hwang

19 August 2025 in Molecules
Verified
Journal Article
Open access
PDF file
JKJun Gu Kim
Jun Gu Kim
JHJae Sang Han
Jae Sang Han
DLDahyeon Lee
Dahyeon Lee
MLMi Kyeong Lee
Mi Kyeong Lee
Bang Yeon HwangBang Yeon Hwang
Bang Yeon Hwang
JLJin Woo Lee
Jin Woo Lee
Twelve undescribed peptidic compounds, bukhansantaibols A–K (1–10) and bukhansantaibals A–B (11–12), were isolated from the soil fungus Trichoderma atroviride through LC-MS and bioactivity-guided purification. Their structures were elucidated by the analysis of 1D and 2D NMR spectra, HRESIMS, and acid hydrolysis using modified Marfey’s method. All compounds were evaluated for their cytotoxic activity against HCT-8 (colon cancer) and SK-OV-3 (ovarian cancer) cells. Among them, compounds 1–5 exhibited significant inhibitory effects, with IC50 values ranging from 2.1 to 19.6 μM.

17 August 2026 in Antioxidants
Verified
Journal Article
Open access
PDF file
KLKyeong Seon Lee
Kyeong Seon Lee
SKSuzy Kim
Suzy Kim
VBVinh Le Ba
Vinh Le Ba
JHJae Sang Han
Jae Sang Han
Bang Yeon HwangBang Yeon Hwang
Bang Yeon Hwang
KLKi Yong Lee
Ki Yong Lee
Neoshirakia japonica, a small deciduous tree belonging to the family Euphorbiaceae, has traditionally been used to relieve pain and fatigue in ancient Asia. To date, there have been no attempts to investigate the overall metabolite profiles of N. japonica. To obtain the phytochemical profiles of its aerial part and root, the extracts were analyzed by UHPLC Orbitrap mass spectrometry, and the metabolites were clustered using feature-based molecular networking (FBMN). The common major constituents of the two different parts were annotated as ellagitannins and ellagic acid derivatives using the GNPS database and SIRIUS software, and a total of 20 compounds were isolated. With FBMN guidance, five minor ginsenosides (10–14) were isolated from the BuOH fraction of the aerial part and first identified in this plant. Also, one new xanthoxylin derivative (16) was discovered from the root, and its antioxidant activity and binding potential to NOX family proteins were evaluated by in silico studies. Consequently, this research aims to provide a comprehensive understanding of the major and minor components of N. japonica by part and suggests its potential as a drug candidate for antioxidant-related diseases.