Lichens, a natural source producing a number of valuable compounds is economically not feasible and profitable due to its slow growth. Mycobiont cultures are alternative sources which have become highly attractive for chemists recently. Mycobiont of sp., a native lichens in Vietnam was separated then cultivated in test tubes. The present study aimed to identify chemical constituents of the cultured mycobiont of sp. Multiple chromatographic methods were applied to isolate three eremophilane sesquiterpenes including one new compound, graphilane () and two known compounds sporogen-AO-1 () and dihydrosporogen-AO-1 (). Their chemical structures was elucidated by extensive 1 D and 2 D NMR analysis and high resolution mass spectroscopy as well as comparisons in literature. Compound was evaluated for the cytotoxic activity against K562 cancer cell line and revealed moderate activity with IC value of 87.20 ± 0.76 µM.
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http://dx.doi.org/10.1080/14786419.2020.1779717 | DOI Listing |
Nat Prod Res
February 2024
Center of Excellence for Innovation in Chemistry (PERCH-CIC), Department of Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, Thailand.
A new eremophilane sesquiterpene, named engleromophilane () together with known eremoxylarin E () and steroids (-) were isolated from the fungus culture. The structures were deduced by the analysis of spectroscopic and MS data, together with the comparison of calculated C NMR chemical shifts and Electronic Circular Dichroism (ECD) spectra. Compound showed cytotoxic effects against Hela, PC-3, HT29 and A549 cell lines with IC in the ranges of 4.
View Article and Find Full Text PDFNat Prod Res
January 2022
Department of Chemistry, Ho Chi Minh City University of Education Ho Chi Minh City Vietname.
Lichens, a natural source producing a number of valuable compounds is economically not feasible and profitable due to its slow growth. Mycobiont cultures are alternative sources which have become highly attractive for chemists recently. Mycobiont of sp.
View Article and Find Full Text PDFFitoterapia
September 2019
School of Pharmaceutical Sciences, South-Central University for Nationalities, Wuhan 430074, China. Electronic address:
Two new sesquiterpenoids, leptosphins A (1) and B (2), and a new cyclopiane diterpene, leptosphin C (3), along with four known diterpenes (4-7) were isolated from the solid fermentation cultures of an endophytic fungus Leptosphaeria sp. XL026 isolated from the leaves of Panax notoginseng. Their structures were elucidated by extensive spectroscopic methods and single-crystal X-ray diffraction (data).
View Article and Find Full Text PDFNat Prod Res
May 2019
a State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, College of Chemistry and Pharmaceutical Sciences , Guangxi Normal University, Guilin , P.R. China.
A new eremophilane sesquiterpene, xylareremophil (1), together with five known eremophilanes, 1α,10α-epoxy-3α-hydroxyeremophil-7(11)-en-12,8β-olide (2), 1,10α,13-trihydroxyeremophil-7(11)-en-12,8-olide (3), 1α,10α-epoxy-13-hydroxyeremophil-7(11)-en-12,8β-olide (4), mairetolides B (5) and G (6) were isolated from the endophytic fungus Xylaria sp. GDG-102 cultured from Sophora tonkinensis. Their structures were elucidated on the basis of spectroscopic data analysis.
View Article and Find Full Text PDFJ Nat Prod
September 2004
Wyeth-Research, 401 North Middletown Road, Pearl River, New York 10965, USA.
07H239-A (1), a new eremophilane sesquiterpene from a marine-derived xylariaceous fungus, was isolated, characterized, and shown to be cytotoxic toward a variety of cancer cell lines, with some selectivity for a CCRFCEM leukemia line (IC(50) = 0.9 microg/mL).
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