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Myrmenaphthol A, Isolated from a Hawaiian Sponge of the Genus Myrmekioderma.


ABSTRACT: Four compounds (1-4) were isolated from a Hawaiian sponge of the genus Myrmekioderma. Myrmenaphthol A (1) incorporates two unusual elements into an oxidized steroidal core: a naphthyl AB-ring system and a hydroxy group at C-2. A comparison of the experimental and predicted electronic circular dichroism (ECD) spectra of 1 assigned an S configuration to the lone stereocenter (?ESI = 0.75; similarity factor 0.8137). Known compounds, cinanthrenol A (2), 3,4-dihydroxypregna-5,17-diene-10,2-carbolactone (3), and 3,4-dihydroxypregna-5,20-diene-10,2-carbolactone (4), were also isolated. Despite literature reports of competitive inhibition at nanomolar levels for 2, neither 2 nor the structurally related 1 showed any activity against estrogen receptors at the concentrations tested.

SUBMITTER: Parrish SM 

PROVIDER: S-EPMC6919962 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature

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Myrmenaphthol A, Isolated from a Hawaiian Sponge of the Genus <i>Myrmekioderma</i>.

Parrish Stephen M SM   Neupane Ram P RP   Harper Mary Kay MK   Head John J   Williams Philip G PG  

Journal of natural products 20190828 9


Four compounds (<b>1</b>-<b>4</b>) were isolated from a Hawaiian sponge of the genus <i>Myrmekioderma</i>. Myrmenaphthol A (<b>1</b>) incorporates two unusual elements into an oxidized steroidal core: a naphthyl AB-ring system and a hydroxy group at C-2. A comparison of the experimental and predicted electronic circular dichroism (ECD) spectra of <b>1</b> assigned an <i>S</i> configuration to the lone stereocenter (Δ<sub>ESI</sub> = 0.75; similarity factor 0.8137). Known compounds, cinanthrenol  ...[more]

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