Unknown

Dataset Information

0

Embellicines C-E: Macrocyclic Alkaloids with a Cyclopenta[b]fluorene Ring System from the Fungus Sarocladium sp.


ABSTRACT: Macrocyclic alkaloids with a cyclopenta[b]fluorene ring system are a relatively young structural class of fungal metabolites, with the first members reported in 2013. Bioassay-guided fractionation of a Sarocladium sp. (fungal strain MSX6737) led to a series of both known and new members of this structural class (1-5), including the known embellicine A (1), three new embellicine analogues (2, 4, and 5), and a semisynthetic acetylated analogue (3). The structures were identified by examining both high-resolution electrospray ionization mass spectrometry data and one-dimensional and two-dimensional NMR spectra. The relative configurations of these molecules were established via 1H-1H coupling constants and nuclear Overhauser effect spectroscopy, while comparisons of the experimental electronic circular dichroism (ECD) spectra with the time-dependent density functional theory ECD calculations were utilized to assign their absolute configurations, which were in good agreement with the literature. These alkaloids (1-5) showed cytotoxic activity against a human breast cancer cell line (MDA-MB-231) that ranged from 0.4 to 4.8 μM. Compounds 1 and 5 were also cytotoxic against human ovarian (OVCAR3) and melanoma (MDA-MB-435) cancer cell lines.

SUBMITTER: Al Subeh ZY 

PROVIDER: S-EPMC10043936 | biostudies-literature | 2023 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Embellicines C-E: Macrocyclic Alkaloids with a Cyclopenta[b]fluorene Ring System from the Fungus <i>Sarocladium</i> sp.

Al Subeh Zeinab Y ZY   Flores-Bocanegra Laura L   Raja Huzefa A HA   Burdette Joanna E JE   Pearce Cedric J CJ   Oberlies Nicholas H NH  

Journal of natural products 20230308 3


Macrocyclic alkaloids with a cyclopenta[b]fluorene ring system are a relatively young structural class of fungal metabolites, with the first members reported in 2013. Bioassay-guided fractionation of a <i>Sarocladium</i> sp. (fungal strain MSX6737) led to a series of both known and new members of this structural class (<b>1</b>-<b>5</b>), including the known embellicine A (<b>1</b>), three new embellicine analogues (<b>2</b>, <b>4</b>, and <b>5</b>), and a semisynthetic acetylated analogue (<b>3  ...[more]

Similar Datasets

| S-EPMC4567992 | biostudies-literature
| S-EPMC8002477 | biostudies-literature
| S-EPMC9698479 | biostudies-literature
| S-EPMC5983305 | biostudies-literature
| S-EPMC3896239 | biostudies-literature
| S-EPMC6669684 | biostudies-literature
| S-EPMC4251527 | biostudies-literature
| S-EPMC4331033 | biostudies-literature
| S-EPMC5923423 | biostudies-literature
| S-EPMC6269681 | biostudies-literature