Abstract
Chemical investigation of the ethyl acetate extract from the marine-derived Streptomyces sp. isolate B1848 resulted in three new isoquinolinequinone derivatives, the mansouramycins E–G (1a–3a), in addition to the previously reported mansouramycins A (5) and D (6). Their structures were elucidated by computer-assisted interpretation of 1D and 2D NMR spectra, high-resolution mass spectrometry, and by comparison with related compounds. Cytotoxicity profiling of the mansouramycins in a panel of up to 36 tumor cell lines indicated a significant cytotoxicity and good tumor selectivity for mansouramycin F (2a), while the activity profile of E (1a) was less attractive.
Document Type
Article
Publication Date
12-20-2021
Digital Object Identifier (DOI)
https://doi.org/10.3390/md19120715
Funding Information
The financial support of this work was funded by a grant from the Bundesministerium für Bildung und Forschung (BMBF, grant 03F0415A).
Related Content
Further data are available on request from the corresponding author.
The following are available online at https://www.mdpi.com/article/10.3390/md19120715/s1, NMR spectra and other supplementary data. They are also available for download as the additional file listed at the end of this record.
Repository Citation
Shaaban, Mohamed; Shaaban, Khaled A.; Kelter, Gerhard; Fiebig, Heinz Herbert; and Laatsch, Hartmut, "Mansouramycins E–G, Cytotoxic Isoquinolinequinones from Marine Streptomycetes" (2021). Center for Pharmaceutical Research and Innovation Faculty Publications. 8.
https://uknowledge.uky.edu/cpri_facpub/8
Supplementary file
Notes/Citation Information
Published in Marine Drugs, v. 19, issue 12, 715.
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).