Reference - Detail
| RRC ID | 89784 |
|---|---|
| Author | Rimkus T, Geisler H, El-Jourani TB, Moumbock AFA, Schiedel M, Reichl S. |
| Title | Benzophenone Derivatives as a New Class of Anti-Infectives Against Acanthamoeba spp. |
| Journal | Arch Pharm (Weinheim) |
| Abstract |
The rare but sight-threatening ocular disease Acanthamoeba keratitis represents a therapeutic challenge due to its causative agents, Acanthamoeba spp., being able to penetrate the corneal epithelium and persist in the corneal stroma as dormant and highly resistant cysts. To combat the scarcity and limitations of current treatment options, we developed a new class of anti-infective agents against Acanthamoeba spp. based on Ro 48-8071 (3), a known inhibitor of the human oxidosqualene cyclase (hOSC). The compound design was guided by docking studies using a homology model of the cycloartenol synthase (CAS), which is the homolog of hOSC found in Acanthamoeba spp. and essential for the parasite's steroid biosynthesis. Among the synthesized Ro 48-8071 analogues, MSHG19 (4f) evoked the most potent activity against Acanthamoeba hatchetti leading to total eradication of trophozoites and cysts at single-digit micromolar concentrations, whereas having no effects within this concentration range on the viability of human corneal epithelial cells. With our initial set of synthesized compounds, we established a first structure-activity relationship model, which nicely aligns with the predicted binding mode of 4f to CAS. Overall, the presented findings highlight the potential of benzophenones as a new class of anti-infectives for the treatment of Acanthamoeba keratitis. |
| Volume | 359(8) |
| Pages | e70321 |
| Published | 2026-8-1 |
| DOI | 10.1002/ardp.70321 |
| PMID | 42622452 |
| PMC | PMC13492222 |
| MeSH | Acanthamoeba* / drug effects Acanthamoeba Keratitis* / drug therapy Acanthamoeba Keratitis* / parasitology Amebicides* / chemical synthesis Amebicides* / chemistry Amebicides* / pharmacology Antiprotozoal Agents* / chemical synthesis Antiprotozoal Agents* / chemistry Antiprotozoal Agents* / pharmacology Benzophenones* / chemical synthesis Benzophenones* / chemistry Benzophenones* / pharmacology Dose-Response Relationship, Drug Humans Molecular Docking Simulation Molecular Structure Parasitic Sensitivity Tests Structure-Activity Relationship |
| Altmetric score |
オルトメトリクス指標項目
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| The most frequently cited source | Bluesky |
| Total number of mentions | 1 |
| Altmetric score changes over past 6months | 0.2 |
| Resource | |
| Human and Animal Cells | HCE-T(RCB2280) |