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miconazole + benzoyl peroxide (Acnidazil / Acne Creme Plus)

✓ Approved

Teva Pharmaceutical Industries Ltd. · 小分子 · 小分子

什么是 miconazole + benzoyl peroxide?

miconazole + benzoyl peroxide 是一种小分子,由Teva Pharmaceutical Industries Ltd.研发。该药已获批,用于治疗相关适应症。

药物档案

商品名Acnidazil, Acne Creme Plus
公司Teva Pharmaceutical Industries Ltd.
药物类别小分子
状态Approved

治疗适应症

miconazole + benzoyl peroxide 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
Skin and subcutaneous tissue disordersAcne✓ Approved

相关研究文献

PubMedFrontiers in cellular and infection microbiology2026-08-05

Downregulation of thioredoxin-like 1 contributes to miconazole's antiviral activity against West Nile virus.

Xia Liancheng L, Luo Zhenghan Z, He Yanhua Y, Peng Haoran H et al.

West Nile virus (WNV)-associated neurological diseases pose a global public health burden, yet no approved antiviral treatments are available. This is primarily due to the challenges of crossing the blood-brain barrier and the lengthy, costly process of drug development. High-throughput screening of a blood-brain barrier-penetrating FDA-approved compound library was performed to identify anti-WNV candidates in a neuronal cell infection model. Antiviral efficacy was further evaluated across different target cells and a range of flaviviruses, as well as in a mouse model of central nervous system (CNS) WNV infection. Stage-of-action analysis and mechanistic studies were conducted. Miconazole emerged as a promising candidate with significant antiviral efficacy against multiple flaviviruses in different cell types. In the CNS infection mouse model, miconazole treatment reduced viral load in brain tissue and improved survival rates. The compound primarily inhibited viral replication, without affecting binding, internalization, or membrane fusion. Mechanistic studies suggested that this antiviral effect may be mediated through the downregulation of host protein thioredoxin-like 1 (TXNL1). Our findings highlight miconazole as a promising candidate for repurposing in anti-flavivirus therapy and identify TXNL1 as a potential host target for the development of broad-spectrum antivirals.

PMID 42553252
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PubMedAngewandte Chemie (International ed. in English)2026-08-05

Defect-Rich CoNi Prussian Blue Analogues Enable Highly Selective Electrochemical Hydrogen Peroxide Production.

Sun Kai K, Mao Yu Y, Zhou Yongfang Y, Wang Ziyun Z et al.

Decentralized electrosynthesis of hydrogen peroxide (H2O2) via the two-electron oxygen reduction reaction (2e- ORR) offers a promising alternative to the traditional anthraquinone process, though developing non-precious metal electrocatalysts with high activity, selectivity, and industrial durability remains challenging. Herein, we report a defect-engineering strategy to synthesize CoNi Prussian blue analogues (PBAs) with precisely tunable [Co(CN)6]3- vacancy concentrations via kinetic trapping. Advanced synchrotron X-ray diffraction and absorption spectroscopy (EXAFS) reveal that these vacancies transform the local coordination of adjacent nickel atoms from saturated octahedral geometries to unsaturated square-planar Ni-N4 motifs. This structural modulation triggers a fundamental shift in the ORR pathway, delivering an H2O2 selectivity exceeding 97% and a remarkable production rate of 6.2 m o l g c a t . - 1 h - 1 in a flow-cell device. Crucially, our defect-rich catalyst demonstrates exceptional durability under a rigorous 120-h variable-current stability test. Density functional theory (DFT) calculations identify the coordinatively unsaturated Ni-N4 sites as the intrinsic active centers, which optimize the binding energy of the *OOH intermediate and suppress the four-electron ORR pathway. This work identifies a robust H2O2 synthesis electrocatalyst and establishes a validated protocol for defect engineering in coordination frameworks.

PMID 42554454
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PubMedAngewandte Chemie (International ed. in English)2026-08-05

Orchestrating Reactive Intermediates: Unlocking Near-Complete Oxidant Utilization in Electrochemical-Thermal Cascade Oxime Synthesis.

Ye Wenkai W, Qiu Yuefeng Y, Jiang Peng P, Li Jingwen J et al.

Oxime synthesis via hydroxylamine is the preferred route and is conventionally achieved by ammoxidation of ammonia with hydrogen peroxide. Yet, in alkaline environments, the simultaneous presence of ionic hydroperoxide (OOH-) and molecular H2O2 severely constrains oxidant efficiency. Here, we introduce a life cycle control strategy that coordinates the generation, stabilization, transport, and consumption of OOH- to concentrate it into a centralized OOH- population. Implemented in a continuous electrochemical-thermal cascade operating in weakly protic methanol, this approach enables efficient oxime production directly from ammonia and offers a route to reengineer traditional manufacturing. Detailed mechanistic studies show that the centralized OOH- population yields an oxidant utilization efficiency of up to 96.8% and a 60.3% enhancement in oxime synthesis rate versus conventional thermocatalysis. By establishing a paradigm for regulating the population of a key reactive intermediate, this work delivers guiding principles for the rational design of advanced cascade catalytic systems.

PMID 42554486
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PubMedFrontiers in immunology2026-08-05

The "two flowers therapy": clinical efficacy and mechanisms of a total glucosides of paeony -colchicine dual-drugs for Behçet's disease derived from Chinese physicians' medication experience.

Liu Can C, Li Lei L, Sun Qinlong Q, Zhang Yixuan Y et al.

To elucidate the synergistic mechanism of "Two flowers therapy" - a Behçet's disease (BD) treatment regimen used in China for more than 30 years, namely Total Glucosides of Paeony (TGP)-colchicine - and its efficacy, safety in BD with mucocutaneous involvement. A retrospective clinical cohort study integrated with computational biology was performed. Five bioactive components were chosen, among which four were from TGP and one was colchicine; 31 overlapping BD-related targets were identified via multi-omics, finally 6 core genes confirmed. 355 BD patients were divided into combination group (CG, n=231) and monotherapy group (MG, n=124). Four active components of TGP (oxypaeoniflorin, albiflorin, benzoyl paeoniflorin, paeoniflorin) and colchicine constituted five bioactive compounds. A total of 837 BD-related targets were retrieved from GeneCards, with 31 overlapping targets between the five compounds and BD. A PPI network (31 nodes, 197 edges) was constructed, and core targets (MMP9, ICAM1, FGF2, TLR4, EGFR, NOS3) were identified. Molecular docking confirmed their high affinity: colchicine formed hydrogen bonds with EGFR, ICAM1, NOS3 (2.2-3.4 Å) and hydrophobic interactions with TLR4; TGP components formed 2-4 hydrogen bonds with EGFR, FGF2, MMP9 (2.2-3.9 Å). GO analysis involved inflammation- and immune-related biological processes; KEGG identified 10 enriched pathways (including Lipid and atherosclerosis, AGE-RAGE) regulating inflammation, immunity and vascular function. Clinically, CG had superior early (M1-M2) efficacy: oral ulcer prevalence was 0.0% vs. 21.0% (M1) and 0.0% vs. 100.0% (M2), genital ulcer prevalence 0.9% vs. 6.5% (M1) (all p<0.05). Both groups achieved complete ulcer resolution from M3. ESR in CG was significantly lower at M2 (p<0.001), with no CRP difference. CG had transient diarrhea; no drug-associated cytopenia was reported in either group. TGP combined with colchicine, a regimen used in China for more than 30 years, exerts therapeutic effects on BD by regulating core targets and inflammatory pathways. Clinically, this regimen more effectively controls early mucocutaneous lesion recurrence in BD patients, with good long-term efficacy and safety.

PMID 42553344
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PubMedThe journal of adhesive dentistry2026-08-05

Influence of Tooth Whitening After Resin Infiltration on the Shear Bond Strength of Orthodontic Brackets.

Schoppmeier Christoph Matthias CM, Sun Li L, Janson Malin M, Graf Isabelle I et al.

To determine the influence of different bleaching methods on the shear bond strength (SBS) of orthodontic brackets bonded to resin-infiltrated (Icon, DMG) extracted human enamel. 64 extracted wisdom teeth were randomized into four groups (n = 16): 1. (-)control (no treatment), 2. (+)control (RI), 3. RI followed by 25% H2O2 (IOB) and 4. RI followed by 10% carbamide peroxide bleaching (HB). After a standardized demineralization protocol, RI and bleaching were performed according to the manufacturer's instructions prior to storage for 14 days. Brackets (Mini Diamond Twin, Ormco) were bonded buccally and lingually (Transbond XT, 3M). SBS values (MPa, traverse speed 0.5 mm/min, Zwick Roell) and the Adhesive Remnant Index (ARI) were determined on the buccal side. Following 5000 thermal cycles (5-55°C; RC 20 CS Lauda), SBS and ARI values for the lingual brackets were determined analogously. Data were analyzed with mixed ANOVA and Kruskal-Wallis and Wilcoxon tests at a 0.05 significance level. Differences in SBS were observed among groups (F(3, 64) = 8.01, P 0.001). HB exhibited the lowest SBS values (14.99 ± 6.42 MPa; 10.84 ± 3.61 MPa), differing significantly from the negative control (P = 0.041; P = 0.002 after thermocycling). No significant differences were noted between IOB and HB. Thermocycling reduced SBS values across all groups (F(3, 64) = 25.83, P 0.001). RI followed by bleaching negatively impacts bracket bonding strength, with a significant reduction observed after home bleaching, while in-office bleaching showed no such effect.

PMID 42554081
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PubMedFrontiers in microbiology2026-08-05

Pleiotropic roles of the MATE transporter CD20030 in Clostridioides difficile: linking multidrug resistance to oxidative stress defense and virulence regulation.

Deng Jie J, Chen Fa Hui FH, Wu Wen Jing WJ, Huang Ting Yu TY et al.

The multidrug-resistant pathogen Clostridioides difficile (C. difficile) presents a persistent clinical threat. While Multidrug and Toxic Compound Extrusion (MATE) transporters are recognized as xenobiotic efflux pumps, their pleiotropic roles in pathogen physiology, particularly in stress adaptation and virulence regulation, remain largely unexplored. Understanding how C. difficile adapts and thrives in the face of host defenses and antimicrobial pressures, potentially influencing gut microbiome dynamics, is crucial for combating C. difficile infection. We functionally characterized the MATE transporter gene CD20030 (mate) in C. difficile 630. A markerless deletion mutant (Δmate) and a complemented strain were constructed using a CRISPR-Cas9 system. Phenotypic assays determining antimicrobial susceptibility, oxidative stress tolerance, autolysis, and cytotoxicity were integrated with comparative proteomic profiling to assess the physiological changes. The Δmate mutant demonstrated broad-spectrum hypersensitivity to antibiotics and hydrogen peroxide, indicating the involvement of this transporter in intrinsic resistance and oxidative defense. The mutant exhibited reduced autolysis; however, toxin production (tcdA and tcdB) and cytotoxicity were significantly upregulated. In soft agar assays, the mutant showed expanded surface spreading. Proteomic data identified a >10,000-fold downregulation of flagellar structural proteins (FliC, FlgC) and a concurrent upregulation of the surface adhesin CwpV. This molecular evidence indicates a "swimming-to-sliding transition" driven by metabolic stress, rather than active swimming motility. These phenotypic and proteomic shifts present a resource reallocation strategy, where the bacterium sacrifices energy-consuming flagellar assembly to prioritize survival and virulence, potentially altering its interaction with the gut epithelial surface and resident microbiota. The MATE transporter (CD20030) operates as a pleiotropic regulatory hub and metabolic sentinel in C. difficile. Its absence induces metabolic reprogramming that orchestrates a motility-virulence trade-off, linking multidrug resistance directly to bacterial pathogenesis. These physiological adaptations likely dictate the pathogen's colonization and persistence strategies within the gut niche, potentially perturbing the host-microbiome equilibrium during infection.

PMID 42553733
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