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Journal of Asian Natural Products Research Volume 23, 2021 - Issue 11
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Research Article

Antimicrobial and antioxidant chlorinated azaphilones from mangrove Diaporthe perseae sp. isolated from the stem of Chinese mangrove Pongamia pinnata

Shah Iram Niaza Institute of Chemical Sciences, Gomal University, Dera Ismail Khan 20950, Pakistan;f School of Marine Sciences, Sun Yat-sen University, Guangzhou 510006, ChinaCorrespondence[email protected] [email protected]
,
Dilfaraz Khana Institute of Chemical Sciences, Gomal University, Dera Ismail Khan 20950, PakistanCorrespondence[email protected] [email protected]
,
Rubina Naza Institute of Chemical Sciences, Gomal University, Dera Ismail Khan 20950, Pakistan
,
Kamran Safdara Institute of Chemical Sciences, Gomal University, Dera Ismail Khan 20950, Pakistan
,
Sheikh Zain Ul Abidinb Institute of Biological Sciences, Gomal University, Dera Ismail Khan 20950, Pakistan
,
Inam Ullah Khanc Faculty of Veternary Sciences, Institute of Microbiology, Gomal University, Dera Ismail Khan 29050, Pakistan
,
Rukhsan Guld Department of Chemistry, Kohat University of Science and Technology, Kohat 26000, Pakistan
,
Wasim Ullah Khane State Key Laboratory of Optoelectronic Materials and Technologies, School of Materials, Science and Engineering, Sun Yat-sen University, Guangzhou 510275, P.R. China
,
Malik Aman Ullah Khana Institute of Chemical Sciences, Gomal University, Dera Ismail Khan 20950, Pakistan
&
Liu Lanf School of Marine Sciences, Sun Yat-sen University, Guangzhou 510006, China
 show all
Pages 1077-1084 | Received 19 Jul 2020, Accepted 09 Oct 2020, Published online: 03 Nov 2020
 
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Abstract

Many plants remain unexplored for their endophytic fungi that may possess potentially important phytochemicals. Consequently, we have focused to discover new natural products from endophytic fungus Diaporthe perseae sp. isolated from the stem of the Chinese mangrove Pongamia pinnata (L.) Pierre plant that led to the isolation of one new chlorinated isochromophilone G (1) along with six known azaphilones (2–7). The structures of the isolated compounds were elucidated by UV, NMR and Mass spectroscopic analysis. All the isolated compounds were screened for their antimicrobial and anti-oxidant activities.

Graphical Abstract

Disclosure statement

No potential conflict of interest was reported by the authors.

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