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Prenylated Phenol and Benzofuran Derivatives from Aspergillus terreus EN-539, an Endophytic Fungus Derived from Marine Red Alga Laurencia okamurai
by
Li, Hong-Lei
, Wang, Bin-Gui
, Li, Xiao-Ming
, Meng, Ling-Hong
, Li, Xin
, Yang, Sui-Qun
in
Absolute configuration
/ Acids
/ Algae
/ Anti-Bacterial Agents - pharmacology
/ antibacterial activity
/ Aquatic bacteria
/ Aspergillus - chemistry
/ Aspergillus terreus
/ Bacteria
/ Bacteria - drug effects
/ Benzofuran
/ Benzofurans - chemistry
/ Benzofurans - pharmacology
/ Chemical synthesis
/ Configurations
/ Endophytes
/ endophytic fungus
/ Fungi
/ Hydrocarbons
/ Laurencia
/ laurencia okamurai
/ Magnetic Resonance Spectroscopy
/ Metabolites
/ Minimum inhibitory concentration
/ Molecular Structure
/ Natural products
/ NMR
/ Nuclear magnetic resonance
/ Optical properties
/ Optical rotation
/ Phenol - chemistry
/ Phenol - pharmacology
/ Phenols
/ Phenols - chemistry
/ Phenols - pharmacology
/ prenylated phenol
/ Rotation
/ Spectrometry
/ Time dependence
/ Two dimensional analysis
2019
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Prenylated Phenol and Benzofuran Derivatives from Aspergillus terreus EN-539, an Endophytic Fungus Derived from Marine Red Alga Laurencia okamurai
by
Li, Hong-Lei
, Wang, Bin-Gui
, Li, Xiao-Ming
, Meng, Ling-Hong
, Li, Xin
, Yang, Sui-Qun
in
Absolute configuration
/ Acids
/ Algae
/ Anti-Bacterial Agents - pharmacology
/ antibacterial activity
/ Aquatic bacteria
/ Aspergillus - chemistry
/ Aspergillus terreus
/ Bacteria
/ Bacteria - drug effects
/ Benzofuran
/ Benzofurans - chemistry
/ Benzofurans - pharmacology
/ Chemical synthesis
/ Configurations
/ Endophytes
/ endophytic fungus
/ Fungi
/ Hydrocarbons
/ Laurencia
/ laurencia okamurai
/ Magnetic Resonance Spectroscopy
/ Metabolites
/ Minimum inhibitory concentration
/ Molecular Structure
/ Natural products
/ NMR
/ Nuclear magnetic resonance
/ Optical properties
/ Optical rotation
/ Phenol - chemistry
/ Phenol - pharmacology
/ Phenols
/ Phenols - chemistry
/ Phenols - pharmacology
/ prenylated phenol
/ Rotation
/ Spectrometry
/ Time dependence
/ Two dimensional analysis
2019
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Prenylated Phenol and Benzofuran Derivatives from Aspergillus terreus EN-539, an Endophytic Fungus Derived from Marine Red Alga Laurencia okamurai
by
Li, Hong-Lei
, Wang, Bin-Gui
, Li, Xiao-Ming
, Meng, Ling-Hong
, Li, Xin
, Yang, Sui-Qun
in
Absolute configuration
/ Acids
/ Algae
/ Anti-Bacterial Agents - pharmacology
/ antibacterial activity
/ Aquatic bacteria
/ Aspergillus - chemistry
/ Aspergillus terreus
/ Bacteria
/ Bacteria - drug effects
/ Benzofuran
/ Benzofurans - chemistry
/ Benzofurans - pharmacology
/ Chemical synthesis
/ Configurations
/ Endophytes
/ endophytic fungus
/ Fungi
/ Hydrocarbons
/ Laurencia
/ laurencia okamurai
/ Magnetic Resonance Spectroscopy
/ Metabolites
/ Minimum inhibitory concentration
/ Molecular Structure
/ Natural products
/ NMR
/ Nuclear magnetic resonance
/ Optical properties
/ Optical rotation
/ Phenol - chemistry
/ Phenol - pharmacology
/ Phenols
/ Phenols - chemistry
/ Phenols - pharmacology
/ prenylated phenol
/ Rotation
/ Spectrometry
/ Time dependence
/ Two dimensional analysis
2019
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Prenylated Phenol and Benzofuran Derivatives from Aspergillus terreus EN-539, an Endophytic Fungus Derived from Marine Red Alga Laurencia okamurai
Journal Article
Prenylated Phenol and Benzofuran Derivatives from Aspergillus terreus EN-539, an Endophytic Fungus Derived from Marine Red Alga Laurencia okamurai
2019
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Overview
Three new prenylated phenol derivatives, terreprenphenols A-C (
-3), along with four known related compounds (
-
), were isolated from
EN-539, an endophytic fungus obtained from the marine red alga
. The structures of these compounds were established by extensive analysis of 1D/2D NMR data, mass spectrometric data, and optical rotation (OR). The corresponding relationship between absolute configuration and optical rotation for known compounds anodendroic acid (
) and asperterreusine C (
) was ambiguous in literature, and their absolute configurations were therefore discussed and confirmed for the first time by time-dependent density functional (TDDFT) ECD and OR calculations. Compounds
-
inhibited some common aquatic bacteria with MIC values ranging from 2 to 64 μg/mL.
Publisher
MDPI AG,MDPI
Subject
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