李援朝(研究员)的个人简介
李援朝,1975年毕业于上海第一医学院药学系药学专业;1982年毕业于兰州大学化学系有机化学专业,获理学硕士学位;1991年毕业于中科院北京化学研究所有机化学专业,获理学博士学位。1975年至1979年福建省医药研究所工作;1983年至1988年福建省医学科学研究所工作,助理研究员;1991年起进入中国科学院上海药物研究所工作至今,任研究课题组组长、研究员、博士研究生导师。
基本信息
姓 名: 李援朝
通讯地址: 上海市浦东新区祖冲之路555号
研究方向
以研发创新新药为主要方向,主要着重于具有抗炎、免疫调节与抗肿瘤作用的新药基础与应用研究。以我国丰富的动植物资源为基础,利用天然产物中具有生物活性的物质作为先导化合物,从分离提取,化学结构鉴定、修饰与改造,化学合成及探索构效关系着手,研究与寻找具有以下几方面的新药。
抗肿瘤免疫调节药物。
器官移植后的抗排异药物。
探索由炎症引起的老年性痴呆治疗药物。
自身免疫系统引起的疾病如类风湿性关节炎、红斑狼疮等的治疗药物。
专家类别
研究员
职务
中科院上海药物所研究员、博士生导师、研究组长
承担科研项目情况
国家科技部重大专项重大新药创制项目:一类新药“雷腾舒”(LLDT-8)的临床前研究,2009年1月―2010年12月。
上海市科委重点科技攻关计划:第四代孕激素屈螺酮的立体专一性合成新工艺研发,2007年10月―2010年9月。
上海市科委重大项目:强效免疫抑制剂--雷公藤手性优化产物新药开发与研究,2003年10月―2005年12月。
上海市科委攻关计划:免疫抑制剂及急性肺损伤药物的研究开发,2003年5月―2004年6月。
代表论著
Bing Zhou, Huanyu Tang, Huijin Feng, Yuanchao Li * First total synthesis of tripdiolide Tetrahedron
Bin Zhang, Hongli Chen, Huijin Feng, Yuanchao Li ? Stereoselective construction of a steroid 5α,7α-oxymethylene derivative and its use in the synthesis of eplerenone Steroids
Bing Zhou, Xiaomei Li, Huanyu Tang, Zehong Miao,Huijin Feng and Yuanchao Li* Total synthesis of novel D-ring-modified triptolide analogues:tructureu2013cytotoxic activity relationship studies on the D-ring of triptolide Organic & Biomolecular Chemistry
Ya-Xi Yang, Zheng Li, Guo-Rong Chen, Yuan-Chao Li*. Phase-Transfer Catalysed Enantioselective Epoxidation of Estra-Δ5(10),9(11)-diene Using Chiral Ammonium Salts Derived from Cinchona Alkaloids. Letters in Organic Chemistry, 2010,7,163-167
Bing Zhou, Zehong Miao, Gang Deng, Jian Ding, Yaxi Yang, Huijin Feng, Yuanchao Li* Synthesis and biological evaluation of novel triptolide analogues for anticancer activity Bioorganic & Medicinal Chemistry Letters
Ya-Xi Yang, Zheng Li, Hui-Jin Feng, Guo-Rong Chen, Yuan-Chao Li,* Concise synthesis of five-membered ring carbasugars based on key ring-closing metathesis Tetrahedron Letters
Bing Zhou, XiaomeiLi, HuijinFeng, YuanchaoLi,* Efficient synthesis of the key intermediate triptophenolide methyl ether for the synthesis of(-)-triptolide Tetrahedron
Hongli Chen, Yuanchao Li*, Biao Jiang*, Huijin Feng Isolation and characterization of related impurities in 24-epibrassinolide;Tetrahedron
Zheng Li,Zhao-Li Zhou,Ze-Hong Miao, Li-Ping Lin, Hui-Jin Feng, Lin-Jiang Tong, Jian Ding,* and Yuan-Chao Li* Design, synthesis, and antitumor evaluation of novel triptolide derivatives as potential anticancer agents. J. Med. Chem
Xiao-Long Du,Hong-Li Chen, Hui-jin Feng and Yuan-Chao Li* Stereoselective Total Synthesis of Natural (S)-Bakuchiol and Its Enantiomer Helvetica Chimica Acta
Hongli Chen, Xiaolong Du, Wei Tang, Y u Zhou, Jianping Zuo , Huijin Feng, Yuanchao Li* Synthesis and structure-immunosuppressive activity relationships of bakuchiol and its derivatives Bioorganic& Medicinal Chemistry
Chen H. L.; Li Y. C.* Simple and convenient synthesis of (±)Bakuchiol Lett. Org. Chem
Zheng Li, Gang Deng, Yuan-Chao Li* ZnI2/Et3SiH: A Novel Mild Reduction System for Direct Deoxygenation of Aryl Aldehydes, ketones, and α,β-Unsaturated Enones Synlett
Gang Deng,Zheng Li,Shu-Ying Peng,Li Fang and Yuan-Chao Li* A new route to stereoselective construction of 6β,7β-methylene unit from androst-5-en-7-one Tetrahedron
Fujiang Guo,Huijin Feng,Youfu Wang,Chun Zhang, Yuanchao Li* Characterization of related impurities in megestrol acetate Journal of pharmaceutical and biomedical analysis
Qin Gu, Yun-Hong Zheng, Yuan-Chao Li* Two Novel Approaches toward Stereoselective Introduction of β-Hydroxymethyl Group at the C-7 Position of 5-Androstene Synthesis
Zhi Jie Xue,Ping Chen,Shu Ying Peng and Yuan Chao Li * Synthesis and determination of absolute configuration of tetracetate 4a-carba-D-xylofuranoside Tetrahedron
Guo Fu-jiang and Li Yuan-chao* New Sesquiterpenoids from Lycianthes marlipoensis Helvetica Chimica Acta
Shao Dong、Zou Chun-Yan、Luo Cheng、Tang Xi-Can and Li Yuan-Chao* Synthesis and evaluation of tacrine-E2020 hybrids as acetylcholinesterase inhibitors for the treatment of Alzheimer’s disease Bioorganic & Medicinal Chemistry Letters,
Zheng Yun-Hong and Li Yuan-Chao* Novel Stereoselective Synthesis of 7β-Methyl-Substituted 5-Androstene Derivatives J. Org. Chem