Unknown

Dataset Information

0

Indole Diterpene Derivatives from the Aspergillus flavus GZWMJZ-288, an Endophytic Fungus from Garcinia multiflora.


ABSTRACT: A new indole diterpene, 26-dihydroxyaflavininyl acetate (1), along with five known analogs (2-6) were isolated from the liquid fermentation of Aspergillus flavus GZWMJZ-288, an endophyte from Garcinia multiflora. The structures of these compounds were identified through NMR, MS, chemical reaction, and X-ray diffraction experiments. Enzyme inhibition activity screening found that compounds 1, 4, and 6 have a good binding affinity with NPC1L1, among which compound 6 exhibited a stronger binding ability than ezetimibe at a concentration of 10 µM. Moreover, compound 5 showed inhibitory activity against α-glucosidase with an IC50 value of 29.22 ± 0.83 µM, which is 13 times stronger than that of acarbose. The results suggest that these aflavinine analogs may serve as lead compounds for the development of drugs targeting NPC1L1 and α-glucosidase. The binding modes of the bioactive compounds with NPC1L1 and α-glucosidase were also performed through in silico docking studies.

SUBMITTER: Wang D 

PROVIDER: S-EPMC10707737 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Indole Diterpene Derivatives from the <i>Aspergillus flavus</i> GZWMJZ-288, an Endophytic Fungus from <i>Garcinia multiflora</i>.

Wang Dongyang D   Zhuang Xiaohong X   Yin Ying Y   Wu Dan D   He Wenwen W   Zhu Weiming W   Xu Yanchao Y   Zuo Mingxing M   Wang Liping L  

Molecules (Basel, Switzerland) 20231204 23


A new indole diterpene, 26-dihydroxyaflavininyl acetate (<b>1</b>), along with five known analogs (<b>2</b>-<b>6</b>) were isolated from the liquid fermentation of <i>Aspergillus flavus</i> GZWMJZ-288, an endophyte from <i>Garcinia multiflora</i>. The structures of these compounds were identified through NMR, MS, chemical reaction, and X-ray diffraction experiments. Enzyme inhibition activity screening found that compounds <b>1</b>, <b>4</b>, and <b>6</b> have a good binding affinity with NPC1L1  ...[more]

Similar Datasets

| S-EPMC525135 | biostudies-literature
| S-EPMC9063546 | biostudies-literature
| S-EPMC8002477 | biostudies-literature
| S-EPMC4113809 | biostudies-literature
| S-EPMC9103106 | biostudies-literature
| S-EPMC6222856 | biostudies-literature
| S-EPMC6165285 | biostudies-literature
| S-EPMC9694122 | biostudies-literature
| S-EPMC6100428 | biostudies-literature
| S-EPMC4306942 | biostudies-literature