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donepezil (E 2022 / TK023 / TK 023)

✓ Approved

Eisai Co., Ltd. · ACHE · 小分子

什么是 donepezil?

donepezil 是一种小分子,由Eisai Co., Ltd.研发。该药已获批,用于治疗相关适应症,给药途径:Transdermal。

药物档案

商品名E 2022, TK023, TK 023
公司Eisai Co., Ltd.
药物类别小分子
分子靶点ACHE
给药途径Transdermal
状态Approved

作用机制

分子靶点

donepezil 作用于 1 个分子靶点:

ACHEacetylcholinesterase (Cartwright blood group) (N-ACHE, ACEE)
需要更深入的分析?Noah AI 可解释复杂机制并与同类药物比较。

治疗适应症

donepezil 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Nervous system disordersDementia Alzheimer's typePhase I

相关研究文献

PubMedJournal of intensive care2026-06-13

Feasibility of a nurse-led patch-type electroencephalography monitoring protocol with arterial spin labeling in patients with severe traumatic brain injury: a prospective observational study.

Asami Masahiro M, Nakata Hikaru H, Kondo Ryoichiro R, Nakajima Yukiko Y et al.

Nonconvulsive seizures are clinically important in severe traumatic brain injury but are difficult to detect when continuous electroencephalography (EEG) is not feasible in the intensive care unit. We conducted a prospective observational study to evaluate a nurse-led patch-type EEG protocol, with arterial spin labeling (ASL) magnetic resonance imaging as an exploratory comparator. Patch-type EEG monitoring was feasible in 21 of 24 enrolled patients (87.5%), and both EEG and ASL assessments were evaluable in 16 patients. Electrographic seizures were detected in four patients (25%), with all of them showing corresponding focal hyperperfusion on imaging. These findings suggest that simplified patch-type EEG monitoring is feasible in this setting; however, further studies are warranted to determine the clinical relevance of nurse-led patch-type EEG monitoring.

PMID 42286780
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PubMedNeural networks : the official journal of the International Neural Network Society2026-06-13

FracNeXt: Enhancing visual representation learning in sequence models with fractal wavelets.

Lu Pengfeng P, Kamata Sei-Ichiro SI, Zhang Mengyunqiu M

Recent applications of sequence models, such as Transformers and Mamba, in the vision domain have demonstrated promising performance. However, the processes of patch token extraction and token mixing inevitably result in the irreversible loss of spatial information. Existing sequence models for vision tasks rely heavily on residual connections to mitigate this issue, yet they overlook the limitations of residual connections in maintaining frequency stability. To address these challenges, we propose Multiple Wavelet Patch Partition (MWPP), a method that extracts patch tokens while preserving the spatial information within each patch. In addition, we introduce a frequency-aware Selective Wavelet Connection (SWC) to augment residual connections, thereby enhancing frequency stability and compensating for the information loss caused by token mixing. Building on MWPP and SWC, we design FracNeXt, a scalable fractal architecture that integrates both convolution and self-attention as token mixers. Under comparable experimental settings, FracNeXt achieves top-1 accuracies of 76.8% on ImageNet and 81.2% on CIFAR-100. Moreover, it delivers state-of-the-art performance across a variety of tasks, including object detection, optical character recognition, and time-series classification on diverse benchmarks. Furthermore, MWPP improves the F1 score of existing sequence models by up to 3.8%, while the proposed fractal architecture with SWC demonstrates superior robustness with respect to model depth.

PMID 42284826
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PubMedPediatric transplantation2026-06-13

Rethinking Portal Vein Hypoplasia in Pediatric Living Donor Liver Transplantation: Prioritizing Longitudinal Patch Augmentation Over Resection.

Channaoui Aniss A, Béry Viviane V, de Magnée Catherine C, Tambucci Roberto R

PMID 42286882
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PubMedFacial plastic surgery : FPS2026-06-13

Non-Surgical Hair Restoration Options: Current Techniques and Emerging Technologies in Prejuvenation.

Paul Benjamin Curman BC

Aims and Backgrounds: Hair loss is a highly prevalent condition, and patients are increasingly seeking pre-junvination and restoration. This review evaluates contemporary non-surgical hair restoration modalities. Therapeutic strategies have evolved from topical vasodilators to targeted hormonal, regenerative, and device-based interventions reflecting advances in our understanding of follicular biology and technology. Hair follicle cycling is regulated by dermal papilla signaling, epithelial stem cells, and perifollicular vascular and inflammatory environments. Non-surgical therapies include oral and topical pharmacologics, hormonal therapies, platelet-rich plasma (PRP), microneedling, peptide-based treatments, exososomes, nutraceuticals, low-level laser therapy (LLLT), lasers, and transdermal delivery systems. Appropriate candidates include patients with androgenetic alopecia and other non-scarring alopecias; accurate diagnosis is critical. Combination therapy is increasingly utilized to target multiple biologic pathways. Post Operative Care: Minimal downtime is expected; long-term adherence is required. Current and Future Development: Emerging therapies include exosome-based treatments, peptides, and advanced drug delivery platforms. Non-surgical modalities are central to prejuvenation and can delay or complement surgical intervention when appropriately applied.

PMID 42285172
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PubMedInternational journal of pharmaceutics2026-06-13

A dual-microneedle system for integrated continuous glucose monitoring and feedback insulin delivery.

Zhao Kangxun K, Niu Yangguang Y, Cao Xiaoping X, Ma Tianqi T et al.

Effective precision diabetes management requires seamless integration of continuous glucose monitoring and therapeutic intervention. In this study, we present a novel dual-microneedle regulatory system, which combines a biosensing microneedle for real-time interstitial glucose monitoring and a therapeutic microneedle for precise transdermal insulin delivery. The biosensing microneedle utilizes glucose oxidase-functionalized electrodes for continuous glucose sensing (demonstrating a broad linear range of 1-34 mM and a limit of detection of 0.4 mM), while the therapeutic microneedle employs electroosmotic flow to regulate insulin infusion through hollow channels under a constant 5 V voltage. This integrated system was demonstrated to provide accurate glycemic control in diabetic Wistar rat models (achieving a 55 % blood glucose reduction within 144 min and demonstrating high clinical accuracy with 88 % of points in Zone A of the Clarke Error Grid), successfully merging continuous glucose monitoring with on-demand insulin delivery. The proposed system demonstrates a solid proof-of-concept for physically segregated closed-loop regulation, paving the way for the development of miniaturized, wearable artificial pancreas platforms for more effective diabetes management.

PMID 42285381
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PubMedMolecular cell2026-06-13

RNA reinforces condensate nucleation on chromatin to amplify oncogenic transcription.

Budinich Krista A KA, Yao Xinyi X, Gong Chujie C, Song Lele L et al.

Aberrant chromatin-associated condensates have emerged as drivers of transcriptional dysregulation in cancer, yet how extrinsic factors modulate their assembly and function remains poorly understood. Gain-of-function mutations in the chromatin reader ENL ("Eleven-nineteen-leukemia") drive oncogenesis by inducing condensate formation at select target loci. Here, we demonstrate that locally produced transcripts reinforce the nucleation, chromatin engagement, and oncogenic activity of mutant ENL condensates. Mutant ENL binds to RNA in part through a basic patch within its YEATS domain, and this interaction enhances condensate formation in vitro and in cells. Using a chemically inducible condensate displacement and renucleation system, we show that blocking ENL-RNA interactions or transcription impairs condensate reformation at endogenous targets. RNA binding preferentially enhances mutant ENL occupancy and transcriptional bursting at condensate-permissive loci. In mouse models, disrupting RNA binding suppresses mutant ENL-driven oncogenic transcription and leukemogenesis. These findings reveal how chromatin-associated oncogenic proteins hijack local transcripts to reinforce condensate nucleation and drive tumorigenesis.

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