ArticleJournal of computer-aided molecular design2025
Anti-inflammatory potential of Grewialin from Grewia optiva: insights from molecular docking, ADMET, DFT, and in-vitro studies.
Article in Journal of computer-aided molecular design, 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
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
Grewia optiva, a medicinal plant native to northern Pakistan, has traditionally been valued for managing pain and inflammation. Among its bioactive constituents, Grewialin, a compound isolated from the stem bark, has garnered attention as a promising candidate for anti-inflammatory drug development. This study aimed to evaluate the anti-inflammatory potential of Grewialin using a combination of in-silico and in-vitro approaches, focusing on its effects on lipoxygenase (LOX) and neutrophil respiratory burst activity. Furthermore, the pharmacological and toxicological profiles of Grewialin were assessed to support its potential as a lead compound. Structure-based virtual screening identified Grewialin as a potential LOX inhibitor. Molecular docking studies revealed a significant binding score of -6.874 kcal/mol, indicating strong interactions with the active site of the LOX enzyme (5-LOX). ADMET profiling demonstrated its favourable pharmacokinetic and toxicological properties, while density functional theory (DFT) calculations highlighted its balanced electrophilic and nucleophilic properties, reflecting its chemical stability and reactivity. Experimental validation through in vitro assays confirmed Grewialin's potent inhibitory activity against LOX, with an IC50 value of 31.9 ± 0.03 µM. Additionally, Grewialin effectively inhibited neutrophil respiratory burst activity, achieving an IC50 of 317.62 ± 0.059 µM, further supporting its anti-inflammatory potential. These findings position Grewialin as a multifaceted anti-inflammatory agent with dual action targeting LOX and neutrophil respiratory burst activity. The combined in-silico and in-vitro results underscore its potential as a lead compound for developing anti-inflammatory drugs. Further research is warranted to explore its therapeutic mechanisms and optimize its efficacy, bridging traditional medicinal knowledge with modern pharmacological advancements. It is worth mentioning, though, that, in line with the aforementioned dual inhibitory profiles, Grewialin also demonstrated moderate potency (LOX and neutrophil respiratory), thus indicating that additional structural optimization or adequate formulation design is necessary to progress it toward therapeutic development. By leveraging the unique properties of Grewialin, this study contributes to the ongoing pursuit of novel, natural compounds for the effective management of inflammatory diseases. This comprehensive evaluation highlights the significance of Grewia optiva as a source of bioactive compounds, emphasizing the need for further exploration into its pharmacological application.
Indexed as
Identifiers
40699260What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.