ArticleProtoplasma2025
Seaweed-based PPO inhibitors as a new frontier in biological weed control for sorghum cultivation: from ocean to field.
Article in Protoplasma, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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The trial behind it
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Who cites it
4 citing papers in PubMed.
- Comparative transcriptomic analysis identifies conserved abiotic stress-responsive hub genes in Sorghum bicolor.BMC plant biology · 2026Article
- Machine learning-assisted screening of natural product database for the identification of novel chalcone-based derivative as a potent DHODH inhibitor in cancer therapy.Discover oncology · 2026Article
- Discovery of novel peptidomimetics against HSP90-HOP interactions towards improved cancer therapeutics using machine learning strategies.Frontiers in bioinformatics · 2026Article
- Identification of novel dihydroorotate dehydrogenase (DHODH) inhibitors for cancer: computational drug repurposing strategy.BMC pharmacology & toxicology · 2025Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Weed management, particularly of broad-leaf species, poses a significant challenge in sorghum production, potentially causing up to 70.9% yield loss. Conventionally, herbicides are the site-specific weed inhibitors often used to suppress the growth of these weeds. Protoporphyrinogen oxidase (PPO) is an important target for developing novel herbicides with remarkable selectivity against these broad-leaved weeds. In particular, saflufenacil is a selective PPO herbicide that can provide temporary relief. However, their prolonged use could lead to various environmental constraints and the evolution of resistant weeds. Recently, bioherbicides are emerging as an alternative to commercial herbicides with safer environmental profiles and combat resistance. On that note, this study aimed to identify novel and safer bioherbicides derived from seaweeds to outright bans on the use of most synthetic herbicides and address herbicide resistance. High-end computational screening strategies including molecular docking, binding free energy, in-house developed ML-based VS, and herbicide-likeness were used to pinpoint the lead molecule against the wild and mutant (∆G210) type AtPPO. Finally, molecular dynamics simulations were employed to validate the binding kinetics of the hit compound. Indeed, the bromophenol derivative BL003, isolated from brown algae, emerged as the hit compound from our analysis. Remarkably, BL003 demonstrated superior binding affinity and stability compared to saflufenacil against both wild-type AtPPO and the mutant AtPPO
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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.