Archiv der Pharmazie

The discovery of a new nonbile acid modulator of Takeda G protein-coupled receptor 5: An integrated computational approach.

Synthesis of hydroxytyrosol analogs with enhanced antioxidant and cytostatic properties against MG-63 human osteoblast-like cells and their potential implications for bone health.

Exploration of Aromatic Hydrazides as Inhibitors of Human Carbonic Anhydrases.

Nature-Inspired Compounds Targeting Escherichia coli WrbA as Biofilm-Modulating Agents: Computational Design, Synthesis, and Biological Evaluation.

Conjugates of amiridine and salicylic derivatives as promising multifunctional CNS agents for potential treatment of Alzheimer's disease.

脒基脒和水杨酸衍生物的结合物作为有前景的多功能中枢神经系统药物，可用于治疗阿尔茨海默病

Unveiling the Therapeutic Potential of Dulaglutide in Mitigating Tacrolimus-Induced Nephrotoxicity Through Targeting the miR-22/HMGB-1/TLR4/MyD88/NF-κB Trajectory.

揭示度拉糖肽通过靶向 miR-22/HMGB-1/TLR4/MyD88/NF-αB 通路减轻他克莫司诱导的肾毒性的治疗潜力

Insights into podophyllotoxin lactone features: New cyclolignans as potential dual tubulin-topoisomerase II inhibitors.

对鬼臼毒素内酯特性的深入了解：新型环木脂素作为潜在的双重微管蛋白-拓扑异构酶 II 抑制剂

Design, Synthesis, In Vitro, and In Silico Studies of 5-(Diethylamino)-2-Formylphenyl Naphthalene-2-Sulfonate Based Thiosemicarbazones as Potent Anti-Alzheimer Agents.

5-(二乙氨基)-2-甲酰基苯基萘-2-磺酸酯基硫代氨基脲类化合物作为强效抗阿尔茨海默病药物的设计、合成、体外和计算机模拟研究

Isoxazole-Based Compounds Targeting the Taxane-Binding Site of Tubulin.

靶向微管蛋白紫杉烷结合位点的异噁唑类化合物

Development of Potent Type V MAPK Inhibitors: Design, Synthesis, and Biological Evaluation of Benzothiazole Derivatives Targeting p38α MAPK in Breast Cancer Cells.

高效 V 型 MAPK 抑制剂的开发：靶向乳腺癌细胞中 p38α MAPK 的苯并噻唑衍生物的设计、合成和生物学评价