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Phomopsichin A-D; Four New Chromone Derivatives from Mangrove Endophytic Fungus Phomopsis sp. 33.


ABSTRACT: Four new chromone derivatives, phomopsichins A-D (1-4), along with a known compound, phomoxanthone A (5), were isolated from the fermentation products of mangrove endophytic fungus Phomopsis sp. 33#. Their structures were elucidated based on comprehensive spectroscopic analysis coupled with single-crystal X-ray diffraction or theoretical calculations of electronic circular dichroism (ECD). They feature a tricyclic framework, in which a dihydropyran ring is fused with the chromone ring. Compounds 1-5 showed weak inhibitory activities on acetylcholinesterase as well as ?-glucosidase, weak radical scavenging effects on 1,1-diphenyl-2-picrylhydrazyl (DPPH) as well as OH, and weak antimicrobial activities. Compounds 1-4 showed no cytotoxic activity against MDA-MB-435 breast cancer cells. Their other bioactivities are worthy of further study, considering their unique molecular structures.

SUBMITTER: Huang M 

PROVIDER: S-EPMC5128758 | biostudies-literature | 2016 Nov

REPOSITORIES: biostudies-literature

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Phomopsichin A-D; Four New Chromone Derivatives from Mangrove Endophytic Fungus Phomopsis sp. 33.

Huang Meixiang M   Li Jing J   Liu Lan L   Yin Sheng S   Wang Jun J   Lin Yongcheng Y  

Marine drugs 20161122 11


Four new chromone derivatives, phomopsichins A-D (<b>1</b>-<b>4</b>), along with a known compound, phomoxanthone A (<b>5</b>), were isolated from the fermentation products of mangrove endophytic fungus <i>Phomopsis</i> sp. 33#. Their structures were elucidated based on comprehensive spectroscopic analysis coupled with single-crystal X-ray diffraction or theoretical calculations of electronic circular dichroism (ECD). They feature a tricyclic framework, in which a dihydropyran ring is fused with  ...[more]

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