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Chemical constituents from the medicinal herb-derived fungus Chaetomium globosum Km1226.
Chang, Chia-Hao; Hsiao, George; Wang, Shih-Wei; Yen, Juei-Yu; Huang, Shu-Jung; Chi, Wei-Chiung; Lee, Tzong-Huei.
Affiliation
  • Chang CH; Institute of Fisheries Science, College of Life Science, National Taiwan University, Taipei, 10617, Taiwan.
  • Hsiao G; Department of Pharmacology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, 11031, Taiwan.
  • Wang SW; Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, 11031, Taiwan.
  • Yen JY; Department of Medicine, MacKay Medical College, New Taipei City, 25245, Taiwan.
  • Huang SJ; Institute of Biomedical Sciences, Mackay Medical College, New Taipei City, 25245, Taiwan.
  • Chi WC; School of Pharmacy, College of Pharmacy, Kaohsiung, 807378, Taiwan.
  • Lee TH; Department of Chinese Medicine, MacKay Memorial Hospital, Taipei, 10449, Taiwan.
Bot Stud ; 64(1): 34, 2023 Nov 30.
Article in En | MEDLINE | ID: mdl-38030829
ABSTRACT

BACKGROUND:

Endophytic fungi have proven to be a rich source of novel natural products with a wide-array of biological activities and higher levels of structural diversity.

RESULTS:

Chemical investigation on the liquid- and solid-state fermented products of Chaetomium globosum Km1226 isolated from the littoral medicinal herb Atriplex maximowicziana Makino resulted in the isolation of compounds 1-14. Their structures were determined by spectroscopic analysis as three previously undescribed C13-polyketides, namely aureonitol C (1), mollipilins G (2), and H (3), along with eleven known compounds 4-14. Among these, mollipilin A (5) exhibited significant nitric oxide production inhibitory activity in LPS-induced BV-2 microglial cells with an IC50 value of 0.7 ± 0.1 µM, and chaetoglobosin D (10) displayed potent anti-angiogenesis property in human endothelial progenitor cells (EPCs) with an IC50 value of 0.8 ± 0.3 µM.

CONCLUSIONS:

Three previously unreported compounds 1-3 were isolated and identified. Mollipilin A (5) and chaetoglobosin D (10) could possibly be developed as anti-inflammatory and anti-angiogenic lead drugs, respectively.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bot Stud Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bot Stud Year: 2023 Document type: Article Affiliation country: