ArticleMolecules (Basel, Switzerland)2016
2-(2-Phenylethyl)chromone Derivatives of Agarwood Originating from Gyrinops salicifolia.
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 8 papers, 1 of them a synthesis that pooled it.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
8 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.
- Agarwood in the Modern Era: Integrating Biotechnology and Pharmacology for Sustainable Use.International journal of molecular sciences · 2025Pooled it
- Phytochemical Investigation ofPlants (Basel, Switzerland) · 2026Article
- Article
- Towards sustainable agarwood production: integrating microbial interactions, anatomical changes, and metabolite biosynthesis.Journal of industrial microbiology & biotechnology · 2024Review
- Agarotetrol in agarwood: its use in evaluation of agarwood quality.Journal of natural medicines · 2020Article
- Sesquiterpenoids and 2-(2-phenylethyl)chromones respectively acting as α-glucosidase and tyrosinase inhibitors from agarwood of an Aquilaria plant.Journal of enzyme inhibition and medicinal chemistry · 2019Article
- Three New 2-(2-Phenylethyl)chromone Derivatives of Agarwood Originated fromMolecules (Basel, Switzerland) · 2019Article
- Agarwood Induction: Current Developments and Future Perspectives.Frontiers in plant science · 2019Review
Corrections and comments
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Three new2-(2-phenylethyl)chromone derivatives (1-3) and a new2-(2-phenylethenyl)chromone derivative (4), together with two known 2-(2-phenylethyl)chromone derivatives (5-6), were isolated from agarwood originating from Gyrinops salicifolia Ridl. The structures of compounds 1-4 were elucidated by comprehensive spectroscopic techniques (UV, IR, 1D and 2D-NMR) and MS analysis, as well as by comparison with the literature. Compounds 1, 2, and 5 showed moderate cytotoxicity against human tumor K562, BEL-7402, and SGC-7901 cell lines with IC50 values of 5.76 to 20.1 µM.
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Registered trials
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