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Rhizovagine A, an unusual dibenzo-α-pyrone alkaloid from the endophytic fungus Rhizopycnis vagum Nitaf22.


ABSTRACT: Rhizovagine A (1), a novel dibenzo-α-pyrone alkaloid with an unprecedented 5/5/6/6/6 fused pentacyclic skeleton, was isolated from the endophytic fungus Rhizopycnis vagum Nitaf22. The structure was elucidated by comprehensive spectroscopic analysis, in combination with quantum chemical 13C NMR and electronic circular dichroism (ECD) calculations for configurational assignment. A plausible biosynthetic pathway for 1 was proposed. Compound 1 displayed acetylcholinesterase inhibitory activity.

SUBMITTER: Wang A 

PROVIDER: S-EPMC9055612 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

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Rhizovagine A, an unusual dibenzo-α-pyrone alkaloid from the endophytic fungus <i>Rhizopycnis vagum</i> Nitaf22.

Wang Ali A   Zhao Siji S   Gu Gan G   Xu Dan D   Zhang Xuping X   Lai Daowan D   Zhou Ligang L  

RSC advances 20200727 47


Rhizovagine A (1), a novel dibenzo-α-pyrone alkaloid with an unprecedented 5/5/6/6/6 fused pentacyclic skeleton, was isolated from the endophytic fungus <i>Rhizopycnis vagum</i> Nitaf22. The structure was elucidated by comprehensive spectroscopic analysis, in combination with quantum chemical <sup>13</sup>C NMR and electronic circular dichroism (ECD) calculations for configurational assignment. A plausible biosynthetic pathway for 1 was proposed. Compound 1 displayed acetylcholinesterase inhibit  ...[more]

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