ArticleMolecules (Basel, Switzerland)2016
New Cerebroside and Nucleoside Derivatives from a Red Sea Strain of the Marine Cyanobacterium Moorea producens.
Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Antidiabetic and Antioxidant Potential of a New Bisglyceride Derivative Together with Other Compounds from the Root Bark ofMolecules (Basel, Switzerland) · 2026Article
- Unveiling the cytotoxicity of Red SeaPharmaceutical biology · 2025Article
- Didemnosides A and B: Antiproliferative Nucleosides from the Red Sea Marine TunicateMarine drugs · 2025Article
- Chemical diversity of cyanobacterial natural products.Natural product reports · 2025Review
- Antileishmanial and Antiplasmodial Activities of Secondary Metabolites from the Root ofMolecules (Basel, Switzerland) · 2023Article
- Genetic and lipidomic analyses suggest thatAccess microbiology · 2022Article
- The Structural Diversity of Natural Glycosphingolipids (GSLs).Journal of carbohydrate chemistry · 2022Article
- Holospiniferoside: A New Antitumor Cerebroside from The Red Sea CucumberMolecules (Basel, Switzerland) · 2021Article
- Bioactive Diketopiperazines and Nucleoside Derivatives from a Sponge-DerivedMarine drugs · 2019Article
- Glycosylated Natural Products From Marine Microbes.Frontiers in chemistry · 2019Review
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In the course of our ongoing efforts to identify marine-derived bioactive compounds, the marine cyanobacterium Moorea producens was investigated. The organic extract of the Red Sea cyanobacterium afforded one new cerebroside, mooreaside A (1), two new nucleoside derivatives, 3-acetyl-2'-deoxyuridine (2) and 3-phenylethyl-2'-deoxyuridine (3), along with the previously reported compounds thymidine (4) and 2,3-dihydroxypropyl heptacosanoate (5). The structures of the compounds were determined by different spectroscopic studies (UV, IR, 1D, 2D NMR, and HRESIMS), as well as comparison with the literature data. Compounds 1-5 showed variable cytotoxic activity against three cancer cell lines.
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