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Chemical constituents with senolytic activity from the stems of Limacia scandens.
Lee, Hee Ju; Zhang, Mi; Doan, Thi Phuong; Park, Eun-Jin; Nghiem, Duc-Trong; Pham, Ha-Thanh-Tung; Pan, Cheol-Ho; Oh, Won-Keun.
Affiliation
  • Lee HJ; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 08826, Republic of Korea; Natural Product Informatics Research Center, Korea Institute of Science and Technology, Gangneung, 25451, Republic of Korea.
  • Zhang M; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 08826, Republic of Korea.
  • Doan TP; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 08826, Republic of Korea.
  • Park EJ; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 08826, Republic of Korea.
  • Nghiem DT; Department of Botany, Hanoi University of Pharmacy, 000084, Hanoi, Viet Nam.
  • Pham HT; Faculty of Pharmacy, PHENIKAA University, Hanoi, 12116, Viet Nam.
  • Pan CH; Natural Product Informatics Research Center, Korea Institute of Science and Technology, Gangneung, 25451, Republic of Korea.
  • Oh WK; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 08826, Republic of Korea. Electronic address: wkoh1@snu.ac.kr.
Phytochemistry ; 212: 113740, 2023 Aug.
Article in En | MEDLINE | ID: mdl-37236331
While screening senotherapeutics from natural products, seven undescribed chemicals, two syringylglycerol derivatives, two cyclopeptides, one tigliane analogue, and two chromone derivatives, as well as six known compounds were isolated from the stems of Limacia scandens. The structures of compounds were elucidated through spectroscopic data analysis, including 1D and 2D NMR, HRESIMS, and CD data. All compounds were tested in replicative senescent human dermal fibroblasts (HDFs) to determine their potential as senotherapeutic agents to specifically target senescent cells. One tigliane and two chromones derivatives showed senolytic activity, indicating that senescent cells were selectively removed. Especially, 2-{2-[(3'-O-ß-d-glucopyranosyl)phenyl]ethyl}chromone is expected to be a potential senotherapeutics by inducing HDF death, inhibiting the activity of senescence-associated ß-galactosidase (SA-ß-gal) and expressing senescence-associated secretory phenotype (SASP) factors.
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Full text: 1 Database: MEDLINE Main subject: Cellular Senescence / Senotherapeutics Limits: Humans Language: En Journal: Phytochemistry Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Cellular Senescence / Senotherapeutics Limits: Humans Language: En Journal: Phytochemistry Year: 2023 Type: Article