基本信息
郭彬 男 硕导 中国科学院上海药物研究所
电子邮件: guobin@simm.ac.cn
通信地址: 上海市浦东张江祖冲之路555号
邮政编码:
电子邮件: guobin@simm.ac.cn
通信地址: 上海市浦东张江祖冲之路555号
邮政编码:
招生信息
招生专业
100701-药物化学
招生方向
抗感染,抗肿瘤,抗血栓等小分子创新药物研发
教育背景
2007-09--2012-06 中国科学院上海药物研究所 博士学位2003-09--2007-06 武汉大学 学士学位
工作经历
工作简历
2021-10~现在, 中国科学院上海药物研究所, 研究员2014-10~2021-09,中国科学院上海药物研究所, 副研究员2012-07~2014-09,中国科学院上海药物研究所, 助理研究员2007-09~2012-06,中国科学院上海药物研究所, 博士学位2003-09~2007-06,武汉大学, 学士学位
社会兼职
2024-01-01-今,南京中医药大学硕士生导师,
专利与奖励
专利成果
( 1 ) 噁唑烷酮类化合物的无定形物及其制备方法和应用, 2022, 第 1 作者, 专利号: CN114685529A( 2 ) 一种玛巴洛沙韦中间体的制备方法, 2022, 第 3 作者, 专利号: CN114014874A( 3 ) 一种噁唑烷酮类抗菌药物中间体的合成方法, 2020, 第 1 作者, 专利号: CN111471041A( 4 ) 芳香丙酸类衍生物、及其制备方法和用途, 2019, 第 1 作者, 专利号: CN110092774A( 5 ) 苯并噁嗪噁唑烷酮类化合物及其制备方法和用途, 2014, 第 2 作者, 专利号: CN103896963A( 6 ) 新型苯并噁嗪噁唑烷酮类化合物及其制备方法和用途, 2011, 第 4 作者, 专利号: CN102260277A
出版信息
发表论文
(1) Efficient Kilogram-Scale Synthesis of a Novel Oxazolidinone Antibacterial Candidate YG-056SP, ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2023, 第 5 作者(2) Improved Synthesis of Key Intermediate of Baloxavir Marboxil, an Anti-Influenza Drug, CHEMISTRYSELECT, 2022, 第 4 作者(3) Discovery of Thieno2,3-eindazole Derivatives as Novel Oral Selective Estrogen Receptor Degraders with Highly Improved Antitumor Effect and Favorable Druggability, JOURNAL OF MEDICINAL CHEMISTRY, 2022, 第 5 作者(4) Design, Synthesis, and Biological Evaluation of Novel Pyrimido4,5-bindole Derivatives Against Gram-Negative Multidrug-Resistant Pathogens, JOURNAL OF MEDICINAL CHEMISTRY, 2021, 第 5 作者(5) Improved Practical Synthesis of DY-038, an Oral Available Antiplatelet Agent, CHEMISTRYSELECT, 2021, 第 6 作者(6) Improved synthesis of YG-056SP, a potent oxazolidinone antibacterial candidate against multi-drug resistant bacteria, JOURNAL OF CHEMICAL RESEARCH, 2019, 第 7 作者(7) Optimization of P2Y12 Antagonist Ethyl 6-(4-((Benzylsulfonyl)carbamoyl)piperidin-1-yl)-5-cyano-2-methylnicotinate (AZD1283) Led to the Discovery of an Oral Antiplatelet Agent with Improved Druglike Properties, Journal of Medicinal Chemistry, 2019, 第 1 作者(8) Design, Synthesis, and Biological Evaluation of Novel DNA Gyrase-Inhibiting Spiropyrimidinetriones as Potent Antibiotics for Treatment of Infections Caused by Multidrug-Resistant Gram-Positive Bacteria, JOURNAL OF MEDICINAL CHEMISTRY, 2019, 第 6 作者(9) Synthesis and biological evaluation of novel potent FFA1 agonists containing 2,3-dihydrobenzob1,4dioxine, BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2019, 第 4 作者(10) Design and optimization of 2,3-dihydrobenzob1,4dioxine propanoic acids as novel GPR40 agonists with improved pharmacokinetic and safety profiles, BIOORGANIC & MEDICINAL CHEMISTRY, 2018, 第 1 作者(11) Design, synthesis and evaluation of potent G-protein coupled receptor 40 agonists, CHINESE CHEMICAL LETTERS, 2016, 第 2 作者(12) Synthesis and structure���activity relationship studies of novel 6,6,5 tricyclic oxazolidinone derivatives as potential antibacterial agents, BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2015, 第 3 作者(13) Design, Synthesis, and Structure-Activity and Structure-Pharmacokinetic Relationship Studies of Novel 6,6,5 Tricyclic Fused Oxazolidinones Leading to the Discovery of a Potent, Selective, and Orally Bioavailable FXa Inhibitor, JOURNAL OF MEDICINAL CHEMISTRY, 2014, 第 3 作者(14) Synthesis and biological evaluation of novel benzoxazinyl-oxazolidinones as potential antibacterial agents, BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 第 1 作者(15) Solubility-Driven Optimization of (Pyridin-3-yl) Benzoxazinyl-oxazolidinones Leading to a Promising Antibacterial Agent, JOURNAL OF MEDICINAL CHEMISTRY, 2013, 第 1 作者(16) Design, Synthesis, and Structure-Activity Relationship Studies of Highly Potent Novel Benzoxazinyl-Oxazolidinone Antibacterial Agents, JOURNAL OF MEDICINAL CHEMISTRY, 2011, 第 3 作者
科研活动
科研项目
( 1 ) 新型骨架选择性雌激素受体降解剂的发现及抗肿瘤活性研究, 负责人, 国家任务, 2020-01--2023-12( 2 ) 新型抗凝药物FXa抑制剂YG-001临床前研究, 负责人, 地方任务, 2018-04--2021-06( 3 ) 螺环嘧啶三酮类候选药物YSR-284的发现研究, 负责人, 国家任务, 2018-01--2020-12