姓 名: |
向秋萍 |
工作单位: |
附属宁波医院 |
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职 称: |
副研究员 |
职 务: |
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办公电话: |
15521245235 |
邮 箱: |
xiang_qiuping@126.com |
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学科专业: |
药学 |
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研究方向: |
基于靶点的药物设计 |
向秋萍博士主要从事创新药物研发工作,在人工智能药物筛选、药物模拟、成药性先导化合物发现等领域积累了丰富的经验。近年来针对前列腺癌及白血病耐药等重大临床需求,申请人基于表观遗传学溴结构域靶标(CBP、BRD4、TRIM24)进行合理药物设计,已获得几类成药性小分子。目前已在SCI期刊发表论文18篇,以第一作者或通讯作者发表SCI论文7篇,申请专利5项(授权两项)。作为项目负责人承担国家自然科学青年基金,中国博士后面上项目以及省市基金等5项。
2009/9-2013/6 本科,湖南师范大学
2013/9-2016/6 硕士,中国科学院广州生物医药与健康研究院
2016/9-2019/6 博士,中国科学院广州生物医药与健康研究院
2019/7-2021/6 博士后,中国科学院广州生物医药与健康研究院
2019/10-2020/8 博士后,威斯康星大学麦迪逊分校
2021/7-2022/3 助理研究员/副研究员,中国科学院广州生物医药与健康研究院
2022/4-至今 副研究员,国科宁波生命与健康产业研究院
2019年,广东省自然科学奖二等奖(排名第七)
国家自然科学青年基金,2021.01-2023.12,主持。
中国博士后科学基金面上项目,2019.07-2021.06,主持,已结题。
宁波市自然科学基金,2022.09-2025.08,主持。
第一作者或通讯作者论文
[1] Qiuping Xiang# Chao Wang,# Tianbang Wu,# Cheng Zhang, Qingqing Hu, Guolong Luo, Jiankang Hu, Xiaoxi Zhuang, Lingjiao Zou, Hui Shen, Xishan Wu, Yan Zhang, Xiangqian Kong, Jinsong Liu, and Yong Xu*. Design, Synthesis, and Biological Evaluation of 1-(Indolizin-3-yl)ethan-1-ones as CBP Bromodomain Inhibitors for the Treatment of Prostate Cancer. Journal of Medicinal Chemistry, 2022, 65, 785–810.
[2] Hongrui Xu, Guolong Luo, Tianbang Wu, Jiankang Hu, Chao Wang, Xishan Wu, Yan Zhang*, Yong Xu,*, and Qiuping Xiang*. Structural insights revealed by the cocrystal structure of CCS1477 in complex with CBP bromodomain. Biochemical and Biophysical Research Communications, 2022,623,17-22.
[3] Qiuping Xiang#,* Guolong Luo# Cheng Zhang, Qingqing Hu, Chao Wang, Tianbang Wu, Hongrui Xu, Jiankang Hu, Xiaoxi Zhuang, Maofeng Zhang, Shuang Wu, Jinxin Xu, Yan Zhang, Jinsong Liu, and Yong Xu*. Discovery, optimization and evaluation of 1-(indolin-1-yl)ethan-1-ones as novel selective TRIM24/BRPF1 bromodomain inhibitors. European Journal of Medicinal Chemistry, 2022,236,114311.
[4] Qiuping Xiang#, Chao Wang#, Yan Zhang, Xiaoqian Xue, Ming Song, Cheng Zhang, Chenchang Li, Chun Wu, Kuai Li, Xiaoyan Hui, Yulai Zhou, Jeff B. Smaill, Adam V. Patterson, Donghai Wu, Ke Ding, Yong Xu*. Discovery and optimization of 1-(1H-indol-1-yl)ethanone derivatives as CBP/EP300 bromodomain inhibitors for the treatment of castration resistant prostate cancer. European Journal of Medicinal Chemistry, 2018, 147, 238?252.
[5] Qiuping Xiang#, Yan Zhang#, Jiaguo Li#, Xiaoqian Xue, Chao Wang, Ming Song, Cheng Zhang, Rui Wang, Chenchang Li, Chun Wu, Yulai Zhou, Xiaohong Yang, Guohui Li, Ke Ding, and Yong Xu*. Y08060: a selective BET inhibitor for treatment of prostate cancer. ACS Medicinal Chemistry Letters, 2018, 9, 262?267.
[6] Lingjiao Zou#, Qiuping Xiang#, Xiaoqian Xue#, Cheng Zhang, Chenchang Li, Chao Wang, Qiu Li, Rui Wang, Shuang Wu, Yulai Zhou, Yan Zhang, and Yong Xu*. Y08197, a novel and selective CBP and EP300 bromodomain inhibitor for treatment of prostate cancer. Acta Pharmacologica Sinica, 2019, 40, 1436?1447.
[7] Tianbang Wu#, Qiuping Xiang#, Chao Wang#, Chun Wu, Cheng Zhang, Maofeng Zhang, Zhaoxuan Liu, Yan Zhang*, Lin-jiu Xiao*, and Yong Xu*. Y06014 is a selective BET inhibitor for the treatment of prostate cancer. Acta Pharmacologica Sinica, 2021, 42, 2120?2131.