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韩

韩欣 (Xin Han)

zhejiang university邮箱:xinhan@zju.edu.cn
H指数:26
被引数:2,910

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Discovery of a First-in-Class Murine Double Minute 2-Recruiting Positive Transcription Elongation Factor B PROTAC Degrader With Selective Antitumor Activity

发现一种具有选择性抗肿瘤活性的第一类小鼠双微体2招募阳性转录延伸因子B PROTAC降解剂

MedComm
IF10.7
2026-04-090
OAAI
Discovery of a Novel Potent and Orally Efficacious PGK1 Inhibitor C67–47 for the Treatment of Human Pancreatic Cancer

刘, L.; 江, X.; 赵, H.; 杨, H.; 杨, H.; 郭, D.; 罗, S.; 杨, Q.; 李, S.; 吴, L.; 等. 发现一种新型强效且口服有效的PGK1抑制剂C67-47用于治疗人胰腺癌. J. Med. Chem. 2026, 69, 12955–12972. [Google Scholar] [CrossRef] [Scilit]

2026-01-010
PRE
Kill Two Birds with One Stone: An Efficient and Potent AR CBS-Targeted Degrader Reverses Breast Cancer Resistance via Concurrent AR Degradation and ERα Transcriptional Suppression

一石二鸟:一种高效且强效的AR CBS靶向降解剂通过同时降解AR和抑制ERα转录来逆转乳腺癌耐药性

2025-11-010
PRE
Discovery of ARD-1676 as a Highly Potent and Orally Efficacious AR PROTAC Degrader with a Broad Activity against AR Mutants for the Treatment of AR plus Human Prostate Cancer
2023-09-0818
OA
Discovery of ARD-2051 as a Potent and Orally Efficacious Proteolysis Targeting Chimera (PROTAC) Degrader of Androgen Receptor for the Treatment of Advanced Prostate Cancer
2023-06-2919
PRE

研究方向

CRL-E3连接酶-泛素化/拟素化通路小分子抑制剂的研发基于PROTAC技术的靶向蛋白降解剂药物的设计合成及临床前成药性评价。 ·围绕克服肿瘤耐药这一重大临床需求,开展抗癌新药的分子设计合成与开发工作,并实现临床转化