Lv5
960 积分 2024-03-15 加入
Discovery of PKMYT1 Inhibitors with a Novel Scaffold for the Treatment of Triple-Negative Breast Cancer
5小时前
已完结
Synthesis and Antiproliferative Activitiy of Novel Diaryl Ureas Possessing a 4H‐Pyrido[1,2‐a]pyrimidin‐4‐one Group
11小时前
已完结
Discovery of novel 4-trifluoromethyl-2-anilinoquinoline derivatives as potential anti-cancer agents targeting SGK1
4天前
已完结
Design, synthesis, antifungal, and antibacterial evaluation of ferulic acid derivatives bearing amide moiety
4天前
已完结
Design, Synthesis, and Biological Evaluation of Potent and Selective Class IIa Histone Deacetylase (HDAC) Inhibitors as a Potential Therapy for Huntington’s Disease
8天前
已完结
Identification of N-(5-tert-Butyl-isoxazol-3-yl)-N′-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea Dihydrochloride (AC220), a Uniquely Potent, Selective, and Efficacious FMS-Like Tyrosine Kinase-3 (FLT3) Inhibitor
12天前
已完结
Optimization of 1-Methyl-3-(pyridin-3-yl)-1H-indol Derivatives as ROR1 Inhibitors with Improved Activity and Selectivity
16天前
已完结
A Small-Molecule PARP7 Inhibitor Triggers Antitumor Immunity
16天前
已完结
The changing treatment landscape of EGFR-mutant non-small-cell lung cancer
16天前
已完结
The Potential of PARP Inhibitors as Antitumor Drugs and the Perspective of Molecular Design
16天前
已完结
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