![李援朝[中國科學院上海藥物研究所研究員]](/img/4/867/nBnauM3XxgjM5UjM4kTOxMDMwQTMxkDM2ETNyQTNwAzMwIzL5kzL0AzLt92YucmbvRWdo5Cd0FmL0E2LvoDc0RHa.jpg "李援朝[中國科學院上海藥物研究所研究員]")
基本信息
姓 名: 李援朝
通訊地址: 上海市浦東新區祖沖之路555號
研究方向
以研發創新新藥為主要方向，主要著重於具有抗炎、免疫調節與抗腫瘤作用的新藥基礎與套用研究。以我國豐富的動植物資源為基礎，利用天然產物中具有生物活性的物質作為先導化合物，從分離提取，化學結構鑑定、修飾與改造，化學合成及探索構效關係著手，研究與尋找具有以下幾方面的新藥。
抗腫瘤免疫調節藥物。
器官移植後的抗排異藥物。
探索由炎症引起的老年性痴呆治療藥物。
自身免疫系統引起的疾病如類風濕性關節炎、紅斑狼瘡等的治療藥物。
專家類別
研究員
職務
中科院上海藥物所研究員、博士生導師、研究組長
承擔科研項目情況
國家科技部重大專項重大新藥創製項目：一類新藥“雷騰舒”（LLDT-8）的臨床前研究，2009年1月—2010年12月。
上海市科委重點科技攻關計畫：第四代孕激素屈螺酮的立體專一性合成新工藝研發，2007年10月—2010年9月。
上海市科委重大項目：強效免疫抑制劑--雷公藤手性最佳化產物新藥開發與研究，2003年10月—2005年12月。
上海市科委攻關計畫：免疫抑制劑及急性肺損傷藥物的研究開發，2003年5月—2004年6月。
代表論著
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:tructure–cytotoxic 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
