ArticleJournal of natural products2011
Stachylines A-D from the sponge-derived fungus Stachylidium sp.
Article in Journal of natural products, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Marine endophytes: biosynthetic engines for novel bioactive metabolites.Frontiers in microbiology · 2025Review
- Cyclic Tetrapeptides with Synergistic Antifungal Activity from the FungusAntibiotics (Basel, Switzerland) · 2022Article
- New phenol and chromone derivatives from the endolichenic fungusRSC advances · 2021Article
- Marine endophytic fungal metabolites: A whole new world of pharmaceutical therapy exploration.Heliyon · 2021Review
- Article
- Biological activities and variation of symbiotic fungi isolated from Coral reefs collected from Red Sea in Egypt.Mycology · 2020Article
- Biological and Chemical Diversity of Marine Sponge-Derived Microorganisms over the Last Two Decades from 1998 to 2017.Molecules (Basel, Switzerland) · 2020Review
- Isoprenyl phenolic ethers from the termite nest-derived medicinal fungus Xylaria fimbriata.Journal of food and drug analysis · 2019Article
- Unveiling Concealed Functions of Endosymbiotic Bacteria Harbored in the Ascomycete Stachylidium bicolor.Applied and environmental microbiology · 2018Article
- Heteroatom-Heteroatom Bond Formation in Natural Product Biosynthesis.Chemical reviews · 2017Review
- Novel Natural Oximes and Oxime Esters with a Vibralactone Backbone from the Basidiomycete Boreostereum vibrans.ChemistryOpen · 2016Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
The marine-derived fungus Stachylidium sp. was isolated from the sponge Callyspongia cf. C. flammea. Four new, putatively tyrosine-derived and O-prenylated natural products, stachylines A-D (1-4), were obtained from the fungal extract. The structures of 1-4 were elucidated on the basis of extensive spectroscopic analyses. The absolute configuration of compound 2 was established by Mosher's method. Stachyline A (1) possesses a rare terminal oxime group and occurs as an interchangeable mixture of E/Z-isomers.
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Registered trials
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