ArticleToxics2025
An Experimental Study to Assess the Ecotoxicity of Warfarin and Tinzaparin on Meiobenthic Amphipods: Original Taxonomic Data from Saudi Arabia and Computational Modeling.
Article in Toxics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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
1 citing paper in PubMed.
- A graph-based computational approach for modeling physicochemical properties in drug design.Scientific reports · 2025Article
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Authors and funding
9 authors.
Funding
Abstract
In the current research, we examined the effects of warfarin (W1 = 5 mg/L and W2 = 25 mg/L) and tinzaparin (T1 = 5 mg/L and T2 = 25 mg/L) on meiofauna using microcosms. These microcosms were intentionally contaminated with both anticoagulants for one month. The findings indicated that nematodes and amphipods demonstrated the greatest resistance to the two anticoagulants evaluated. Specifically, the number of amphipods increased after exposure to the treatment that included T2. Following the separate introduction of each drug, amphipods displayed a taxonomic restructuring, with a more significant impact observed from T2 and T2W1. Results were derived from multivariate analyses of a compilation of sensitive amphipod taxa in response to tinzaparin and warfarin. In contrast, different species were identified as positive indicators for tinzaparin. Ultimately, the similarity between the control amphipod replicates and those subjected to mixed anticoagulants (T1W1 and T2W2) suggests that warfarin may have reduced the toxicity of tinzaparin. Additionally, the computational study indicated that warfarin interacts with 4XNN and forms strong molecular interactions with several key residues, which contribute to the toxicokinetic characteristics observed in the empirical findings.
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Registered trials
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