Six New Polyketide Decalin Compounds from Mangrove Endophytic Fungus Penicillium aurantiogriseum 328#

Six new compounds with polyketide decalin ring, peaurantiogriseols A–F (1–6), along with two known compounds, aspermytin A (7), 1-propanone,3-hydroxy-1- (1,2,4a,5,6,7,8,8a-octahydro-2,5-dihydroxy-1,2,6-trimethyl-1-naphthalenyl) (8), were isolated from the fermentation products of mangrove endophytic...

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Main Authors: Yanhong Ma, Jing Li, Meixiang Huang, Lan Liu, Jun Wang, Yongcheng Lin
Format: Article
Language:English
Published: MDPI AG 2015-10-01
Series:Marine Drugs
Subjects:
Online Access:http://www.mdpi.com/1660-3397/13/10/6306
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spelling doaj-2c1c44c010a945f686e2e65d77cd261c2020-11-24T23:28:51ZengMDPI AGMarine Drugs1660-33972015-10-0113106306631810.3390/md13106306md13106306Six New Polyketide Decalin Compounds from Mangrove Endophytic Fungus Penicillium aurantiogriseum 328#Yanhong Ma0Jing Li1Meixiang Huang2Lan Liu3Jun Wang4Yongcheng Lin5School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, ChinaSchool of Marine Sciences, Sun Yat-sen University, Guangzhou 510006, ChinaSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, ChinaSchool of Marine Sciences, Sun Yat-sen University, Guangzhou 510006, ChinaSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, ChinaKey Laboratory of Functional Molecules from Oceanic Microorganisms (Sun Yat-sen University), Department of Education of Guangdong Province, Guangzhou 510080, ChinaSix new compounds with polyketide decalin ring, peaurantiogriseols A–F (1–6), along with two known compounds, aspermytin A (7), 1-propanone,3-hydroxy-1- (1,2,4a,5,6,7,8,8a-octahydro-2,5-dihydroxy-1,2,6-trimethyl-1-naphthalenyl) (8), were isolated from the fermentation products of mangrove endophytic fungus Penicillium aurantiogriseum 328#. Their structures were elucidated based on their structure analysis. The absolute configurations of compounds 1 and 2 were determined by 1H NMR analysis of their Mosher esters; the absolute configurations of 3–6 were determined by using theoretical calculations of electronic circular dichroism (ECD). Compounds 1–8 showed low inhibitory activity against human aldose reductase, no activity of inducing neurite outgrowth, nor antimicrobial activity.http://www.mdpi.com/1660-3397/13/10/6306mangrove endophytic fungiPenicillium aurantiogriseumsecondary metabolitespolyketide decalin derivative
collection DOAJ
language English
format Article
sources DOAJ
author Yanhong Ma
Jing Li
Meixiang Huang
Lan Liu
Jun Wang
Yongcheng Lin
spellingShingle Yanhong Ma
Jing Li
Meixiang Huang
Lan Liu
Jun Wang
Yongcheng Lin
Six New Polyketide Decalin Compounds from Mangrove Endophytic Fungus Penicillium aurantiogriseum 328#
Marine Drugs
mangrove endophytic fungi
Penicillium aurantiogriseum
secondary metabolites
polyketide decalin derivative
author_facet Yanhong Ma
Jing Li
Meixiang Huang
Lan Liu
Jun Wang
Yongcheng Lin
author_sort Yanhong Ma
title Six New Polyketide Decalin Compounds from Mangrove Endophytic Fungus Penicillium aurantiogriseum 328#
title_short Six New Polyketide Decalin Compounds from Mangrove Endophytic Fungus Penicillium aurantiogriseum 328#
title_full Six New Polyketide Decalin Compounds from Mangrove Endophytic Fungus Penicillium aurantiogriseum 328#
title_fullStr Six New Polyketide Decalin Compounds from Mangrove Endophytic Fungus Penicillium aurantiogriseum 328#
title_full_unstemmed Six New Polyketide Decalin Compounds from Mangrove Endophytic Fungus Penicillium aurantiogriseum 328#
title_sort six new polyketide decalin compounds from mangrove endophytic fungus penicillium aurantiogriseum 328#
publisher MDPI AG
series Marine Drugs
issn 1660-3397
publishDate 2015-10-01
description Six new compounds with polyketide decalin ring, peaurantiogriseols A–F (1–6), along with two known compounds, aspermytin A (7), 1-propanone,3-hydroxy-1- (1,2,4a,5,6,7,8,8a-octahydro-2,5-dihydroxy-1,2,6-trimethyl-1-naphthalenyl) (8), were isolated from the fermentation products of mangrove endophytic fungus Penicillium aurantiogriseum 328#. Their structures were elucidated based on their structure analysis. The absolute configurations of compounds 1 and 2 were determined by 1H NMR analysis of their Mosher esters; the absolute configurations of 3–6 were determined by using theoretical calculations of electronic circular dichroism (ECD). Compounds 1–8 showed low inhibitory activity against human aldose reductase, no activity of inducing neurite outgrowth, nor antimicrobial activity.
topic mangrove endophytic fungi
Penicillium aurantiogriseum
secondary metabolites
polyketide decalin derivative
url http://www.mdpi.com/1660-3397/13/10/6306
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