朱 进 博士 副教授
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电话:
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传真:
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E-mail: jinz@ecust.edu.cn
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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
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(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.