Comparative in vitro assessment of CYP2C19 inhibition by ilaprazole and conventional proton pump inhibitors using a high throughput fluorometric assay [0.03%]
高效液相色谱法评估伊拉普拉唑与常规质子泵抑制剂对CYP2C19的体外抑制作用
A Priyadharshini,T M Vijayakumar,N Damodharan et al.
A Priyadharshini et al.
The Vivid™ CYP2C19 Blue Screening Kit was utilized, and fluorescence intensity was measured after incubation with PPIs, using ticlopidine as a positive inhibitor control.
Comparative Study
Scientific reports. 2025 May 25;15(1):18158. DOI:10.1038/s41598-025-02872-5 2025
Efficacy and safety of antiplatelet therapy for secondary prevention of small subcortical infarction: A systematic review and network meta-analysis [0.03%]
小腔隙性脑梗死二级预防抗血小板治疗的有效性和安全性系统评价和网络Meta分析
Xiao Feng,Junyong Du,Tong Qu et al.
Xiao Feng et al.
The NMA demonstrated that Cilostazol showed the best efficacy in preventing MACEs (surface under the cumulative ranking curve (SUCRA): 90.0%). cilostazol significantly reduced the incidence of MACEs compared to aspirin (OR, 0.66; 95% CI, 0.49-0.89), ticlopidine (OR, 0.65; 95% CI, 0.43-1.00), dipyridamole
Transcriptome sequencing and Mendelian randomization analysis identified biomarkers related to neutrophil extracellular traps in diabetic retinopathy [0.03%]
转录组测序和孟德尔随机化分析确定了与糖尿病视网膜病变中性粒细胞胞外诱捕网相关的生物标志物
Linlin Hao,Songhong Wang,Lian Zhang et al.
Linlin Hao et al.
Drug predictions targeting P2RY12 suggested prasugrel, ticagrelor, and ticlopidine as potential options owing to their high binding affinity with this key genes.
Ticlopidine protects hepatic ischemia-reperfusion injury via suppressing ferroptosis [0.03%]
替格瑞洛通过抑制铁死亡保护肝脏缺血再灌注损伤
Yanni Ma,Xintong Yao,Yunding Zou et al.
Yanni Ma et al.
Hepatic ischemia-reperfusion injury (IRI) is a major cause of liver damage during hepatic resection, transplantation, and other surgical procedures, often leading to graft failure and liver dysfunction. Recent studies have identified ferrop...
Development of a fluorous trapping reagent for rapid detection of electrophilic reactive metabolites [0.03%]
一种用于快速检测亲电子代谢物的氟表面捕获试剂的开发
Yusuke Akagi,Hiroyuki Yamakoshi,Yoshiharu Iwabuchi
Yusuke Akagi
The highly sensitive mass spectrometric detection of an unprecedented adduct of the ticlopidine metabolite was realized.
Sensitizing methicillin-resistant Staphylococcus aureus (MRSA) to cefuroxime: the synergic effect of bicarbonate and the wall teichoic acid inhibitor ticlopidine [0.03%]
碳酸氢盐和细胞壁胞壁酸抑制剂替克拉宾对耐甲氧西林金黄色葡萄球菌(MRSA)与头孢呋辛的协同作用
Selvi C Ersoy,Richard A Proctor,Warren E Rose et al.
Selvi C Ersoy et al.
Herein, we further investigated the impacts of NaHCO3 exposure on CFX susceptibility in the presence and absence of a WTA synthesis inhibitor, ticlopidine (TCP), in a collection of clinical MRSA isolates from skin and soft tissue infections (SSTI) and bloodstream infections (BSI).
Study of Factors to Increase the Usage Rate of Generic Drugs in Platelet Aggregation Inhibitors [0.03%]
血小板聚集抑制剂中提高通用药物使用率因素的研究
Takaaki Suzuki,Mari Iwata,Mika Maezawa et al.
Takaaki Suzuki et al.
Monthly personal income in each prefecture were negatively correlated with outpatient out-of-hospital and outpatient in-hospital prescriptions of the PAIs clopidogrel (75 mg), cilostazol (50 mg), cilostazol (100 mg), and ticlopidine (100 mg), but not between monthly personal income and outpatient out-of-hospital...prescription of ticlopidine (100 mg)....For outpatient out-of-hospital prescriptions and outpatient in-hospital prescriptions, negative correlation was generally observed between the usage rate of generic drug and monthly personal income, except for ticlopidine (100 mg), which has the lowest price among the brand-name drugs.
Ticlopidine induces embryonic development toxicity and hepatotoxicity in zebrafish by upregulating the oxidative stress signaling pathway [0.03%]
替卡松平通过上调氧化应激信号通路在斑马鱼中诱导发育毒性和肝毒性
Rong Xu,Pengxiang Xu,Haiyan Wei et al.
Rong Xu et al.
Previously, a few studies have shown that ticlopidine can induce liver injury, but the exact mechanism of hepatotoxicity remains unclear....In this study, in order to deeply explore the potential molecular mechanisms of ticlopidine -induced hepatotoxicity, we used zebrafish as a model organism to comprehensively evaluate the hepatotoxicity of ticlopidine and its associated mechanism....Three days post-fertilization, zebrafish larvae were exposed to varying concentrations (1.5, 1.75 and 2 μg/mL) of ticlopidine for 72 h, in contrast, adult zebrafish were exposed exposure to 4 μg/mL of ticlopidine for 28 days....In conclusion, ticlopidine might inhibit normal development and liver proliferation in zebrafish by upregulation of oxidative stress levels, thus leading to embryonic developmental toxicity and hepatotoxicity....In this study, we used zebrafish as a model organism to elucidate the developmental toxicity and hepatotoxicity induced by ticlopidine upregulation of oxidative stress signaling pathway in zebrafish, providing a theoretical basis for clinical application.
Identification of 3 key genes as novel diagnostic and therapeutic targets for OA and COVID-19 [0.03%]
鉴定出3个关键基因作为诊断和治疗OA和COVID-19的新靶点
Yiwei Zhang,Zhengwei Duan,Yonghao Guan et al.
Yiwei Zhang et al.
In addition, niclosamide, ciclopirox, and ticlopidine were found to be potentially useful for the treatment of OA patients infected with SARS-CoV-2.
Synthesis and structure-activity relationships of ticlopidine derivatives and analogs as inhibitors of ectonucleotidase CD39 [0.03%]
噻氯匹定衍生物和类似物作为ecto-核苷酸酶CD39抑制剂的合成及构效关系研究
Chunyang Bi,Laura Schäkel,Salahuddin Mirza et al.
Chunyang Bi et al.
In the present study, we performed an extensive structure-activity relationship (SAR) analysis of ticlopidine derivatives and analogs as CD39 inhibitors followed by an in-depth characterization of selected compounds.
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