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zxp
Lv5
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870 积分
2022-09-27 加入
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Discovery of (4-Pyrazolyl)-2-aminopyrimidines as Potent and Selective Inhibitors of Cyclin-Dependent Kinase 2
3天前
已完结
Design and Synthesis of New bis-oxindole and Spiro(triazole-oxindole) as CDK4 Inhibitors with Potent Anti-breast Cancer Activity
3天前
已完结
CDK inhibitors from past to present: A new wave of cancer therapy
3天前
已完结
Recent development of CDK inhibitors: An overview of CDK/inhibitor co-crystal structures
3天前
已完结
Design and Synthesis of New bis-oxindole and Spiro(triazole-oxindole) as CDK4 Inhibitors with Potent Anti-breast Cancer Activity
10天前
已完结
Discovery of (4-Pyrazolyl)-2-aminopyrimidines as Potent and Selective Inhibitors of Cyclin-Dependent Kinase 2
11天前
已完结
Synthesis of 3‐(2‐Hydroxyaryl)indazole Derivatives through Radical O ‐Arylation and [3,3]‐Rearrangement from N ‐Hydroxyindazoles and Diaryliodonium Salts
11天前
已完结
From Structure Modification to Drug Launch: A Systematic Review of the Ongoing Development of Cyclin-Dependent Kinase Inhibitors for Multiple Cancer Therapy
13天前
已完结
Discovery of PF-06873600, a CDK2/4/6 Inhibitor for the Treatment of Cancer
13天前
已完结
Design and Synthesis of New bis-oxindole and Spiro(triazole-oxindole) as CDK4 Inhibitors with Potent Anti-breast Cancer Activity
13天前
已完结
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