Unknown

Dataset Information

0

Broad-Spectrum Antiviral Natural Products from the Marine-Derived Penicillium sp. IMB17-046.


ABSTRACT: A new pyrazine derivative, trypilepyrazinol (1), a new ?-pyrone polyketide, (+)-neocitreoviridin (2), and a new ergostane analogue, 3?-hydroxyergosta-8,14,24(28)-trien-7-one (3), were isolated and characterized along with five known compounds from the marine-derived fungus Penicillium sp. IMB17-046. The structures of these new compounds were determined using spectroscopic data analyses (HRESIMS, 1D- and 2D-NMR), X-ray crystallography analysis, and TDDFT ECD calculation. Compounds 1 and 3 exhibited broad-spectrum antiviral activities against different types of viruses, including human immunodeficiency virus (HIV), hepatitis C virus (HCV), and influenza A virus (IAV), with IC50 values ranging from 0.5 to 7.7 ?M. Compounds 1 and 2 showed antibacterial activities against Helicobacter pylori, a causative pathogen of various gastric diseases, with minimum inhibitory concentration (MIC) values of 1-16 ?g/mL.

SUBMITTER: Li J 

PROVIDER: S-EPMC6696147 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Broad-Spectrum Antiviral Natural Products from the Marine-Derived <i>Penicillium</i> sp. IMB17-046.

Li Jiao J   Wang Yujia Y   Hao Xiaomeng X   Li Shasha S   Jia Jia J   Guan Yan Y   Peng Zonggen Z   Bi Hongkai H   Xiao Chunling C   Cen Shan S   Gan Maoluo M  

Molecules (Basel, Switzerland) 20190802 15


A new pyrazine derivative, trypilepyrazinol (<b>1</b>), a new α-pyrone polyketide, (+)-neocitreoviridin (<b>2</b>), and a new ergostane analogue, 3β-hydroxyergosta-8,14,24(28)-trien-7-one (<b>3</b>), were isolated and characterized along with five known compounds from the marine-derived fungus <i>Penicillium</i> sp. IMB17-046. The structures of these new compounds were determined using spectroscopic data analyses (HRESIMS, 1D- and 2D-NMR), X-ray crystallography analysis, and TDDFT ECD calculatio  ...[more]

Similar Datasets

| S-EPMC7680217 | biostudies-literature
| S-EPMC9611354 | biostudies-literature
| S-EPMC6470642 | biostudies-literature
| S-EPMC6950740 | biostudies-literature
| S-EPMC8066695 | biostudies-literature
| S-EPMC3144912 | biostudies-literature
| S-EPMC4883660 | biostudies-literature
| S-EPMC6270126 | biostudies-literature
| S-EPMC3857800 | biostudies-literature
| S-EPMC9057218 | biostudies-literature