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Talaromarins A-F: Six New Isocoumarins from Mangrove-Derived Fungus Talaromyces flavus TGGP35.


ABSTRACT: Six new isocoumarin derivative talaromarins A-F (1-6), along with 17 known analogues (7-23), were isolated from the mangrove-derived fungus Talaromyces flavus (Eurotiales: Trichocomaceae) TGGP35. Their structures were identified by detailed IR, UV, 1D/2D NMR and HR-ESI-MS spectra. The absolute configurations of new compounds were determined by the modified Mosher's method and a comparison of their CD spectra with dihydroisocoumarins described in the literature. The antioxidant, antibacterial, anti-phytopathogenic and inhibitory activity against α-glucosidase of all the isolated compounds were tested. Compounds 6-11, 17-19 and 21-22 showed similar or better antioxidant activity than the IC50 values ranging from 0.009 to 0.27 mM, compared with the positive control trolox (IC50 = 0.29 mM). Compounds 10, 18, 21 and 23 exhibited strong inhibitory activities against α-glucosidase with IC50 values ranging from 0.10 to 0.62 mM, while the positive control acarbose had an IC50 value of 0.5 mM. All compounds showed no antibacterial or anti-phytopathogenic activity at the concentrations of 50 μg/mL and 1 mg/mL, respectively. These results indicated that isocoumarins will be useful to developing antioxidants and as diabetes control agents.

SUBMITTER: Cai J 

PROVIDER: S-EPMC9229493 | biostudies-literature | 2022 May

REPOSITORIES: biostudies-literature

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Talaromarins A-F: Six New Isocoumarins from Mangrove-Derived Fungus <i>Talaromyces flavus</i> TGGP35.

Cai Jin J   Zhu Xiao-Chen XC   Zeng Wei-Nv WN   Wang Bin B   Luo You-Ping YP   Liu Jing J   Chen Min-Jing MJ   Li Gao-Yu GY   Huang Guo-Lei GL   Chen Guang-Ying GY   Xu Jing J   Zheng Cai-Juan CJ  

Marine drugs 20220527 6


Six new isocoumarin derivative talaromarins A-F (<b>1</b>-<b>6</b>), along with 17 known analogues (<b>7</b>-<b>23</b>), were isolated from the mangrove-derived fungus <i>Talaromyces flavus</i> (Eurotiales: Trichocomaceae) TGGP35. Their structures were identified by detailed IR, UV, 1D/2D NMR and HR-ESI-MS spectra. The absolute configurations of new compounds were determined by the modified Mosher's method and a comparison of their CD spectra with dihydroisocoumarins described in the literature.  ...[more]

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