TY - JOUR
T1 - Antibacterial activity, cytotoxicity and chemotaxonomic significance of chemical constituents from Alsophila manniana Hook R.M.Tryon (Cyatheaceae) rhizomes
AU - Tsepeupon Matchide, Marie G.
AU - Sonfack Fozeng, Herman D.
AU - Tchuente Tchuenmogne, Marthe A.
AU - Djadock Anensong, Claudelle S.
AU - Wembe Koagne, Wilfried
AU - Anthonissen, Stijn
AU - Mba Nguekeu, Yves M.
AU - Do, Kiep Minh
AU - Lee, Yuan E.
AU - Dehaen, Wim
AU - Morita, Hiroyuki
AU - Tene, Mathieu
AU - Ngouela, Silvère Augustin
AU - Awouafack, Maurice Ducret
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/6
Y1 - 2024/6
N2 - Phytochemical investigation of Alsophila manniana rhizomes led to the isolation of twelve known compounds, including two triterpenes (1 and 2), four steroids (3–6), one glycerol (7), three phenols (8–10), and two flavonoids (11 and 12). Their structures were elucidated by analyses of the NMR and MS data and by comparisons with those in the literature. Their antibacterial and cytotoxic activities were evaluated against Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus, and Bacillus subtilis; and on human lung A549, cervical HeLa, and breast MCF-7 cancer cell lines, respectively. Fractions FD and FF had significant activities against E. coli (MIC = 75 μg/mL) and K. pneumoniae (MICs = 75 and 37.5 μg/mL). Compounds 3 and 7–12 had moderate antibacterial activities with MIC values ranging from 75 to 150 μg/mL against the bacteria. All samples were inactive against all tested human cancer cell lines, even at 100 μg/mL. This is the first investigation of the chemical constituents of A. manniana, as well as the first report of compounds 3, 7, and 10–12 from the genus Alsophila. The chemotaxonomic significance of these compounds is discussed.
AB - Phytochemical investigation of Alsophila manniana rhizomes led to the isolation of twelve known compounds, including two triterpenes (1 and 2), four steroids (3–6), one glycerol (7), three phenols (8–10), and two flavonoids (11 and 12). Their structures were elucidated by analyses of the NMR and MS data and by comparisons with those in the literature. Their antibacterial and cytotoxic activities were evaluated against Escherichia coli, Klebsiella pneumoniae, Staphylococcus aureus, and Bacillus subtilis; and on human lung A549, cervical HeLa, and breast MCF-7 cancer cell lines, respectively. Fractions FD and FF had significant activities against E. coli (MIC = 75 μg/mL) and K. pneumoniae (MICs = 75 and 37.5 μg/mL). Compounds 3 and 7–12 had moderate antibacterial activities with MIC values ranging from 75 to 150 μg/mL against the bacteria. All samples were inactive against all tested human cancer cell lines, even at 100 μg/mL. This is the first investigation of the chemical constituents of A. manniana, as well as the first report of compounds 3, 7, and 10–12 from the genus Alsophila. The chemotaxonomic significance of these compounds is discussed.
KW - Alsophila manniana
KW - Biological activities
KW - Chemotaxonomic significance
KW - Cyatheaceae
KW - Secondary metabolites
UR - http://www.scopus.com/inward/record.url?scp=85191456484&partnerID=8YFLogxK
U2 - 10.1016/j.bse.2024.104834
DO - 10.1016/j.bse.2024.104834
M3 - 学術論文
AN - SCOPUS:85191456484
SN - 0305-1978
VL - 114
JO - Biochemical Systematics and Ecology
JF - Biochemical Systematics and Ecology
M1 - 104834
ER -