2019
DOI: 10.1016/j.fitote.2019.104260
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Four new metabolites from the endophytic fungus Diaporthe lithocarpus A740

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Cited by 19 publications
(19 citation statements)
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“…(Pleosporaceae) isolated from medicinal plant M. officinalis produced two new metabolites, isobenzofuranone A 61 Their structures contain a 12-carbon atoms polyketide skeleton unit-linked, through an amide bond, with a derivative of L-isoleucine, a rare compound class [116]. The endophytic fungus D. pseudomangiferae retrieved from leaves of Sabicea cinerea species found along forest edges in the French Guiana, produces four metabolites: mycoepoxydiene (114) and altiloxin A (115), as well as enamidin (116) and eremofortin F (117) [117]. A filamentous fungus of the genus Diaporthe associated with the seeds of Cinchona ledgeriana, from West Java-Indonesia, produces cinchona alkaloids: quinine (118), quinidine (119), cinchonidine (120) and cinchonine (121), upon cultivation in a synthetic liquid medium [118][119][120][121][122].…”
Section: J Fungi 2020 6 X For Peer Review 3 Of 31mentioning
confidence: 99%
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“…(Pleosporaceae) isolated from medicinal plant M. officinalis produced two new metabolites, isobenzofuranone A 61 Their structures contain a 12-carbon atoms polyketide skeleton unit-linked, through an amide bond, with a derivative of L-isoleucine, a rare compound class [116]. The endophytic fungus D. pseudomangiferae retrieved from leaves of Sabicea cinerea species found along forest edges in the French Guiana, produces four metabolites: mycoepoxydiene (114) and altiloxin A (115), as well as enamidin (116) and eremofortin F (117) [117]. A filamentous fungus of the genus Diaporthe associated with the seeds of Cinchona ledgeriana, from West Java-Indonesia, produces cinchona alkaloids: quinine (118), quinidine (119), cinchonidine (120) and cinchonine (121), upon cultivation in a synthetic liquid medium [118][119][120][121][122].…”
Section: J Fungi 2020 6 X For Peer Review 3 Of 31mentioning
confidence: 99%
“…Bioassay-guided fractionation of ethyl acetate extract from D. pseudomangifera, by cytotoxic effects against mammalian cancer cells allowed the isolation of the mycoepoxydien (114), which showed cytotoxic activity with IC 50 values of 7.5, 17.7, and 15.8 µM against against human uterine cervical carcinoma KB and MDA-MB-435 cells, respectively. The compound eremofortin F (117) was cytotoxic on KB (IC 50 = 13.9 µM) and MRC5 (IC 50 = 12.2 µM) cells [117].…”
Section: Cytotoxic Activitymentioning
confidence: 99%
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