Complete Structure and Total Synthesis of Streptospherin A, a Cancer Stem Cell Inhibitor

Streptospherin A (1), isolated from the actinomycete Streptomyces sp. KUSC-240 strain, inhibits cancer stem cell sphere formation. The planar structure of 1 and the relative configurations of C3, C5, and C7 in the pyran ring were previously assigned as (3R*, 5S*, 7S*). However, the remaining relative stereochemistry and absolute configuration of 1 have not been determined because of limited sample availability. In this study, the relative configuration at C2 was established by synthesizing model compounds 15a/15b and comparing their NMR spectra with that of 1. The absolute configuration of 1 was then confirmed by total synthesis. Synthetic 1 exhibited inhibitory activity of cancer stem cell sphere formation equivalent to that of the natural 1.

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Publication Details

Journal
Chemistry - A European Journal
Published
2026-04-14
DOI
https://doi.org/10.1002/chem.71002
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Complete Structure and Total Synthesis of Streptospherin A, a Cancer Stem Cell Inhibitor

Hiroaki Ikeda, Hideaki Kakeya, Takefumi Kuranaga, Taiki Suo et al.
Chemistry - A European Journal
Microbial Natural Products and Biosynthesis
article

Complete Structure and Total Synthesis of Streptospherin A, a Cancer Stem Cell Inhibitor

Hiroaki Ikeda, Hideaki Kakeya, Takefumi Kuranaga, Taiki Suo, Saya Yoshida, Rakuto Ohta
article en

Abstract

Streptospherin A (1), isolated from the actinomycete Streptomyces sp. KUSC-240 strain, inhibits cancer stem cell sphere formation. The planar structure of 1 and the relative configurations of C3, C5, and C7 in the pyran ring were previously assigned as (3R*, 5S*, 7S*). However, the remaining relative stereochemistry and absolute configuration of 1 have not been determined because of limited sample availability. In this study, the relative configuration at C2 was established by synthesizing model compounds 15a/15b and comparing their NMR spectra with that of 1. The absolute configuration of 1 was then confirmed by total synthesis. Synthetic 1 exhibited inhibitory activity of cancer stem cell sphere formation equivalent to that of the natural 1.

Chemistry - A European Journal
Kyoto University (JP), Kyoto Pharmaceutical University (JP)
Japan Agency for Medical Research and Development
Openalex Percentile: Top 12%
Microbial Natural Products and Biosynthesis
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