Lv33
390 积分 2025-07-16 加入
Multi-therapies Based on PARP Inhibition: Potential Therapeutic Approaches for Cancer Treatment
4小时前
已完结
Discovery of Quinazoline-2,4(1H,3H)-dione Derivatives Containing 3-Substituted Piperizines as Potent PARP-1/2 Inhibitors─Design, Synthesis, In Vivo Antitumor Activity, and X-ray Crystal Structure Analysis
4小时前
已完结
Discovery of quinazoline-2,4(1H,3H)-dione derivatives as novel PARP-1/2 inhibitors: design, synthesis and their antitumor activity
4小时前
已完结
Discovery of Aryloxyphenyl–Heptapeptide Hybrids as Potent and Selective Matrix Metalloproteinase-2 Inhibitors for the Treatment of Idiopathic Pulmonary Fibrosis
21小时前
已完结
Discovery of TP0597850: A Selective, Chemically Stable, and Slow Tight-Binding Matrix Metalloproteinase-2 Inhibitor with a Phenylbenzamide–Pentapeptide Hybrid Scaffold
21小时前
已完结
Discovery of Highly Potent and Selective Matrix Metalloproteinase-7 Inhibitors by Hybridizing the S1′ Subsite Binder with Short Peptides
21小时前
已完结
Discovery of a Novel Series of Tankyrase Inhibitors by a Hybridization Approach
1天前
已完结
Pyrimidine derivatives in discovery of pesticides: A review
4天前
已完结
Design, Synthesis, and Structure–Activity Relationship of Novel LSD1 Inhibitors Based on Pyrimidine–Thiourea Hybrids As Potent, Orally Active Antitumor Agents
4天前
已完结
Multi-therapies Based on PARP Inhibition: Potential Therapeutic Approaches for Cancer Treatment
4天前
已完结
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