| 朱 进 博士 副教授
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个人简介
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2000.9-2003.7 沈阳药科大学，理学学士/理学硕士 2003.7-2006.12 华中科技大学同济药学院，讲师 2007.3-2009.6 华东理工大学药学院，医学博士 2009.6-至今 华东理工大学药学院制药工程系，讲师，副教授 研究方向
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1. 药物设计与合成 2. 有机小分子催化反应 以第一或通讯作者身份发表的代表性论著
-------------------------------------------------------------------------------- (1) the ethylene bis-dithiocarbamate fungicide mancozeb activates voltage-gated kcnq2 potassium channel. toxicol. lett. 2013, 219, 211−217. (2) design and synthesis of small molecular dual inhibitor of falcipain-2 and dihydrofolate reductase as antimalarial agent. bioorg. med. chem. lett. 2012, 22, 958−962.
(3) direct oxidative conversion of 3-aryl propionaldehydes to 3-aryl acroleins promoted by somo catalysis.tetrahedron lett. 2012, 53, 1207−1209.
(4) 1-(2,6-dibenzyloxybenzoyl)-3-(9h-fluoren-9-yl)-urea: a novel cyclophilin a allosteric activator. biochem. biophy. res. commun. 2012, 425, 938−943.
(5) 2-(3,4-dihydro-4-oxothieno[2,3-d]pyrimidin-2-ylthio)acetamides as a new class of falcipain-2 inhibitors. 3. design, synthesis and biological evaluation. molecules. 2009, 14, 785−797.
(6) refinement and 3d-qsar studies of inhibitors of cyclophilin a containing amide linker. qsar comb. sci. 2009, 28, 183−193.
(7) a direct amine-palladium acetate cocatalyzed saegusa oxidation reaction of unmodified aldehydes to α,β-unsaturated aldehydes. adv. synth. catal. 2009, 351, 1229−1232. | 
