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Unique Polyhalogenated Peptides from the Marine Sponge Ircinia sp.

Two new bromopyrrole peptides, haloirciniamide A (1) and seribunamide A (2), have been isolated from an Indonesian marine sponge of the genus Ircinia collected in the Thousand Islands (Indonesia). The planar structure of both compounds was assigned on the basis of extensive 1D and 2D NMR spectroscop...

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Autores principales: Fernández, Rogelio, Bayu, Asep, Aryono Hadi, Tri, Bueno, Santiago, Pérez, Marta, Cuevas, Carmen, Yunovilsa Putra, Masteria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460063/
https://www.ncbi.nlm.nih.gov/pubmed/32731567
http://dx.doi.org/10.3390/md18080396
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author Fernández, Rogelio
Bayu, Asep
Aryono Hadi, Tri
Bueno, Santiago
Pérez, Marta
Cuevas, Carmen
Yunovilsa Putra, Masteria
author_facet Fernández, Rogelio
Bayu, Asep
Aryono Hadi, Tri
Bueno, Santiago
Pérez, Marta
Cuevas, Carmen
Yunovilsa Putra, Masteria
author_sort Fernández, Rogelio
collection PubMed
description Two new bromopyrrole peptides, haloirciniamide A (1) and seribunamide A (2), have been isolated from an Indonesian marine sponge of the genus Ircinia collected in the Thousand Islands (Indonesia). The planar structure of both compounds was assigned on the basis of extensive 1D and 2D NMR spectroscopy and mass spectrometry. The absolute configuration of the amino acid residues in 1 and 2 was determined by the application of Marfey’s method. Compound 1 is the first dibromopyrrole cyclopeptide having a chlorohistidine ring, while compound 2 is a rare peptide possessing a tribromopyrrole ring. Both compounds failed to show significant cytotoxicity against four human tumor cell lines, and neither compound was able to inhibit the enzyme topoisomerase I or impair the interaction between programmed cell death protein PD1 and its ligand, PDL1.
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spelling pubmed-74600632020-09-02 Unique Polyhalogenated Peptides from the Marine Sponge Ircinia sp. Fernández, Rogelio Bayu, Asep Aryono Hadi, Tri Bueno, Santiago Pérez, Marta Cuevas, Carmen Yunovilsa Putra, Masteria Mar Drugs Article Two new bromopyrrole peptides, haloirciniamide A (1) and seribunamide A (2), have been isolated from an Indonesian marine sponge of the genus Ircinia collected in the Thousand Islands (Indonesia). The planar structure of both compounds was assigned on the basis of extensive 1D and 2D NMR spectroscopy and mass spectrometry. The absolute configuration of the amino acid residues in 1 and 2 was determined by the application of Marfey’s method. Compound 1 is the first dibromopyrrole cyclopeptide having a chlorohistidine ring, while compound 2 is a rare peptide possessing a tribromopyrrole ring. Both compounds failed to show significant cytotoxicity against four human tumor cell lines, and neither compound was able to inhibit the enzyme topoisomerase I or impair the interaction between programmed cell death protein PD1 and its ligand, PDL1. MDPI 2020-07-28 /pmc/articles/PMC7460063/ /pubmed/32731567 http://dx.doi.org/10.3390/md18080396 Text en © 2020 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fernández, Rogelio
Bayu, Asep
Aryono Hadi, Tri
Bueno, Santiago
Pérez, Marta
Cuevas, Carmen
Yunovilsa Putra, Masteria
Unique Polyhalogenated Peptides from the Marine Sponge Ircinia sp.
title Unique Polyhalogenated Peptides from the Marine Sponge Ircinia sp.
title_full Unique Polyhalogenated Peptides from the Marine Sponge Ircinia sp.
title_fullStr Unique Polyhalogenated Peptides from the Marine Sponge Ircinia sp.
title_full_unstemmed Unique Polyhalogenated Peptides from the Marine Sponge Ircinia sp.
title_short Unique Polyhalogenated Peptides from the Marine Sponge Ircinia sp.
title_sort unique polyhalogenated peptides from the marine sponge ircinia sp.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460063/
https://www.ncbi.nlm.nih.gov/pubmed/32731567
http://dx.doi.org/10.3390/md18080396
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