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Anti-Inflammatory, Antiallergic and COVID-19 Main Protease (Mpro) Inhibitory Activities of Butenolides from a Marine-Derived Fungus Aspergillus costaricaensis.


ABSTRACT: Amid the current COVID-19 pandemic, the emergence of several variants in a relatively high mutation rate (twice per month) strengthened the importance of finding out a chemical entity that can be potential for developing an effective medicine. In this study, we explored ethyl acetate (EtOAc) extract of a marine-derived fungus Aspergillus cosatricaensis afforded three butenolide derivatives, butyrolactones I, VI and V (1-3), two naphtho-γ-pyrones, TMC-256 A1 (4) and rubrofusarin B (5) and methyl p-hydroxyphenyl acetate (6). Structure identification was unambiguously determined based on exhaustive spectral analyses including 1D/2D NMR and mass spectrometry. The isolated compounds (1-6) were assessed for their in vitro anti-inflammatory, antiallergic, elastase inhibitory activities and in silico SARS-CoV-2 main protease (Mpro). Results exhibited that only butenolides (1 and 2) revealed potent activities similar to or more than reference drugs unlike butyrolactone V (3) suggesting them as plausible chemical entities for developing lead molecules.

SUBMITTER: Uras IS 

PROVIDER: S-EPMC9111082 | biostudies-literature | 2022 Mar

REPOSITORIES: biostudies-literature

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Anti-Inflammatory, Antiallergic and COVID-19 Main Protease (M<sup>pro</sup>) Inhibitory Activities of Butenolides from a Marine-Derived Fungus <i>Aspergillus costaricaensis</i>.

Uras Ibrahim S IS   Korinek Michal M   Albohy Amgad A   Abdulrazik Basma S BS   Lin Wenhan W   Ebada Sherif S SS   Konuklugil Belma B  

ChemistrySelect 20220328 12


Amid the current COVID-19 pandemic, the emergence of several variants in a relatively high mutation rate (twice per month) strengthened the importance of finding out a chemical entity that can be potential for developing an effective medicine. In this study, we explored ethyl acetate (EtOAc) extract of a marine-derived fungus <i>Aspergillus cosatricaensis</i> afforded three butenolide derivatives, butyrolactones I, VI and V (<b>1</b>-<b>3</b>), two naphtho-<i>γ</i>-pyrones, TMC-256 A1 (<b>4</b>)  ...[more]

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