New aminoglycoside from the aerial parts of <i>Ruehssia caatingae</i> (Apocynaceae)

A new aminoglycoside N-Galacted Amino Acid, (3-methylpentanoic acid-<i>β</i>-<i>D</i>-galactofuranoside) <b>(1)</b> and two previously identified metabolites, (-)-conduritol F <b>(2)</b> and thymidine <b>(3),</b> were isolated of dried aerial parts of <i>R. caatingae</i> (Apocynaceae). The structure elucidation of these compounds was based on analyses of spectroscopic data including 1D, 2D NMR, IR and HR-ESI-MS techniques and by comparing their NMR data with those reported in the literature. Furthermore, the cytotoxic potential of compounds <b>1</b>, <b>2</b> and <b>3</b> was evaluated by testing them against a panel of glioblastoma (U87-MG), neuroblastoma (SH-SY5Y) and breast adenocarcinoma (MDA-MB-231) cancer cell lines. All substances tested did not promote a minimum cytotoxicity of 50% in the tumour cell lines submitted to this assay.

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Publication Details

Journal
Natural Product Research
Published
2025-11-19
DOI
https://doi.org/10.1080/14786419.2025.2588800
Primary Topic
Traditional and Medicinal Uses of Annonaceae
Type
article
Field-Weighted Citation Impact
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article

New aminoglycoside from the aerial parts of Ruehssia caatingae (Apocynaceae)

José Maria Barbosa‐Filho, José Iranildo Miranda de Melo, Thalisson Amorim de Souza, Daniele Idalino Janebro et al.
Natural Product Research
Traditional and Medicinal Uses of Annonaceae
article

New aminoglycoside from the aerial parts of Ruehssia caatingae (Apocynaceae)

José Maria Barbosa‐Filho, José Iranildo Miranda de Melo, Thalisson Amorim de Souza, Daniele Idalino Janebro, Jociano da Silva Lins, S Almeida, Marcelo Sobral da Silva, Igor Gabriel da Silva Ramalho, Josean Fechine Tavares
article en

Abstract

A new aminoglycoside N-Galacted Amino Acid, (3-methylpentanoic acid-<i>β</i>-<i>D</i>-galactofuranoside) <b>(1)</b> and two previously identified metabolites, (-)-conduritol F <b>(2)</b> and thymidine <b>(3),</b> were isolated of dried aerial parts of <i>R. caatingae</i> (Apocynaceae). The structure elucidation of these compounds was based on analyses of spectroscopic data including 1D, 2D NMR, IR and HR-ESI-MS techniques and by comparing their NMR data with those reported in the literature. Furthermore, the cytotoxic potential of compounds <b>1</b>, <b>2</b> and <b>3</b> was evaluated by testing them against a panel of glioblastoma (U87-MG), neuroblastoma (SH-SY5Y) and breast adenocarcinoma (MDA-MB-231) cancer cell lines. All substances tested did not promote a minimum cytotoxicity of 50% in the tumour cell lines submitted to this assay.

Natural Product Research
Universidade Estadual da Paraíba (BR), Universidade Federal da Paraíba (BR)
Openalex Percentile: Top 66%
Traditional and Medicinal Uses of Annonaceae
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