An Oxazole Alkaloid, Terpenoids, and Cyclodipeptides with Cytotoxic and NO Inhibitory Effects from a Mangrove-Derived Fungus Trichoderma sp. GXT-22.1.

Autor: Anh DV; Vietnam Academy of Science and Technology, Institute of Marine Biochemistry, 18 Hoang Quoc Viet, 10072, Hanoi, VIET NAM., Anh DH; Vietnam Academy of Science and Technology, Institute of Marine Biochemistry, 18 Hoang Quoc Viet, Cau Giay, 10072, Hanoi, VIET NAM., Vien LT; Vietnam Academy of Science and Technology, Institute of Marine Biochemistry, 18 Hoang Quoc Viet, Cau Giay, 10072, Hanoi, VIET NAM., Huong PTM; Vietnam Academy of Science and Technology, Institute of Marine Biochemistry, 18 Hoang Quoc Viet, Cau Giay, 10072, Hanoi, VIET NAM., Cuong NX; Vietnam Academy of Science and Technology, Institute of Marine Biochemistry, 18 Hoang Quoc Viet, Cau Giay, 10072, Hanoi, VIET NAM., Ngan NTT; Vietnam Academy of Science and Technology, Institute of Genome Research, 18 Hoang Quoc Viet, Cau Giay, 10072, Hanoi, VIET NAM., Tung NN; Vietnam Academy of Science and Technology, Center for High Technology Research and Development, 18 Hoang Quoc Viet, Cau Giay, 10072, Hanoi, VIET NAM., Quang TH; Vietnam Academy of Science and Technology, Institute of Marine Biochemistry, 18 Hoang Quoc Viet, 10072, Hanoi, VIET NAM.
Jazyk: angličtina
Zdroj: Chemistry & biodiversity [Chem Biodivers] 2024 Dec 13, pp. e202402986. Date of Electronic Publication: 2024 Dec 13.
DOI: 10.1002/cbdv.202402986
Abstrakt: Chemical investigation of the mangrove-derived fungus Trichoderma sp. GXT-22.1 led to isolation and identification of 10 secondary metabolites, including one new compound, 5'-(4-methoxyphenyl)-1',3'-oxazole (1), one new natural compound, (E)-6,10-dimethyl-5-undecene-2,9,10-triol (2), along with eight known compounds, tricholumin A (3), harzianol J (4), cyclonerodiol (5), 10,11-dihydro-11-hydroxycyclonerodiol (6), cyclonerodiol B (7), epicyclonerodiol oxide (8), cyclo(Val-Pro) (9), and cyclo-(4-hydroxyprolinyl-leucine) (10). The structural feature of oxazole in 1 was unusually found among the fungal metabolites. Compounds 1 and 4 exhibited weak cytotoxicity toward HepG2 and MCF-7 human carcinoma cell lines at the concentration of 100 μM, with induction of 41.5 ± 3.0 and 39.3 ± 2.3% cell death, respectively. Compounds 1-5, 8 and 10 showed their inhibitory effect against NO overproduction in LPS-stimulated RAW264.7 cells, with IC50 values ranging from 37.5 ± 2.6 to 86.5 ± 5.1 μM. Molecular docking simulation suggested that 1 inhibit NO overproduction via modulating the action of iNOS protein.
(© 2024 Wiley‐VCH GmbH.)
Databáze: MEDLINE
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