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个人简介

教育经历 1988.7-1992.7 大连理工大学 化工学院 工学学士 1992.9-1995.7 大连理工大学 化工学院 工学硕士 1995.9-1998.7 中国科学院上海药物研究所 理学博士 工作经历 1998.8-1999.8 威斯康星大学 药学院 研究助理 1999.9-2001.12 中国科学院上海药物研究所 副研究员 课题组长 2002.1-2005.6 中国科学院上海药物研究所 研究员 课题组长 2005.7-至今 华东师范大学 研究员

研究领域

酶活前药系统 新一代抗体偶联药物

近期论文

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近期论文 Synthesis and biological evaluation of novel quaternary ammonium antibody drug conjugates based on camptothecin derivatives, PLoS ONE, 2023, 18(12): e0292871 Development of HSP90 inhibitors-SN38 conjugates for cancer treatment, Bioorganic Chemistry 137 (2023) 106582 Design and synthesis of multivalent drug delivery system with CA IX inhibitors as ligands, Bioorganic & Medicinal Chemistry 93 (2023) 117456 Design, synthesis, and biological evaluation of BRD4 degraders, Bioorganic & Medicinal Chemistry 78 (2023) 117134 Design, synthesis, and biological evaluation of 4?(1H?1,2,3?triazol?1?yl) benzamides as HSP90 inhibitors, Molecular Diversity (2023) 27:239–248 代表性论文 给药系统 SN38-based albumin-binding prodrug for efficient targeted cancer chemotherapy, Journal of Controlled Release, 2021, 339, 297-306 A camptothecin-based albumin-binding prodrug enhances efficacy and safety in vivo, European Journal of Medicinal Chemistry, 2021, 226, 113851 An HSP90 inhibitor based fluorescent probe for selective tumor targeting, Dyes and Pigments, 2021, 196, 109783 A water-soluble probe with p-hydroxybenzyl quaternary ammonium linker for selective imaging in senescent cells, Analytica Chimica Acta, 2020, 133, 99-108 A Novel Multifunctional 2-Nitroinmidazole-based Bioreductive Linker and its Application in Hypoxia-Activated Prodrug, Bioorganic Chemistry, 2020, 101, 193975 Design, synthesis and biological evaluation of HSP90 inhibitor SN38 conjugates for targeted drug accumulation, Journal of Medicinal Chemistry, 2020, 53, 5421-5441 Optimized HSP90 mediated fluorescent probes for cancer-specific bioimaging, Journal of Materials Chemistry B, 2020, 8, 1878—1896 Enhanced cellular uptake efficiency of DCM probes or SN38 conjugating with phenylboronic acids, Bioorganic & Medicinal Chemistry, 2020, 28, 115377 Synthesis and biological evaluation of paclitaxel and vorinostat co-prodrugs for overcoming drug resistance in cancer therapy in vitro, Bioorganic & Medicinal Chemistry,2019, 27(7), 1405-1413 A series of camptothecin prodrugs exhibit HDAC inhibition activity, Bioorganic & Medicinal Chemistry, 2018, 26, 4706–4715 Synthesis and Biological Evaluation of Paclitaxel and Camptothecin Prodrugs on the Basis of 2-Nitroimidazole, ACS Medicinal Chemistry Letters, 2017, 8 (7), 762–765 Synthesis and biological evaluation of hypoxia-activated prodrugs of SN-38, European Journal of Medicinal Chemisty, 2017, 132, 135-141 Carbamoylmannose enhances the tumor targeting ability of supramolecular nanoparticles formed through host–guest complexation of a pair of homopolymers, Journal of Materials Chemistry B, 2017, 5, 83 10-Boronic acid substituted camptothecin as prodrug of SN-38, European Journal of Medicinal Chemistry, 2016, 116, 84-89 Design, Synthesis, and Biological Evaluation of New Cathepsin B-Sensitive Camptothecin Nanoparticles Equipped with a Novel Multifuctional Linker, Bioconjugate Chemistry, 2016, 27(5), 1267-1275 Synthesis and biological evaluation of bis and monocarbonate prodrugs of 10-hydroxycamptothecins, Bioorganic & Medicinal Chemistry, 2004, 12, 4003-4008 Camptothecin derivative-loaded poly(caprolactone-co-lactide)-b-PEG-b-poly(caprolactone-co-lactide) nanoparticles and their biodistribution in mice, Journal of Controlled Release, 2004, 96, 135-148 药物化学 Design, synthesis, and biological evaluation of Wee1 kinase degraders, European Journal of Medicinal Chemistry, 2022, 243, 114786 Synthesis and fluorescent studies of a low molecular weight rotor for living cancer cell imaging, Dyes and Pigments, 2020, 178,108353 Design, synthesis and biological evaluation of the thioether-containing lenalidomide analogs with anti-proliferative activities, European Journal of Medicinal Chemistry, 2019, 176,419-430 Pyrazolo[4,3-b]pyrimido[4,5-e][1,4]diazepine derivatives as new multi-targeted inhibitors of Aurora A/B and KDR, European Journal of Medicinal Chemistry, 2018, 158, 428-441 Design and synthesis of aryloxypropanolamine as b3-adrenergic receptor antagonist in cancer and lipolysis, European Journal of Medicinal Chemistry, 2018, 150, 757-770 Design, synthesis and biological evaluation of colchicine derivatives as novel tubulin and histone deacetylase dual inhibitors, European Journal of Medicinal Chemistry, 2015, 95, 127-135. Design, synthesis and biological evaluation of novel homocamptothecin analogues as potent antitumor agents, Bioorganic & Medicinal Chemistry, 2015, 23,1950-1962 Suzuki coupling based synthesis and in vitro cytotoxic evaluation of 7-heteroaryl-substituted camptothecin analogs, Bioorganic & Medicinal Chemistry Letters, 2014, 24, 1597-1599 The discovery and optimization of novel dual inhibitors of topoisomerase ii and histone deacetylase, Bioorganic & Medicinal Chemistry, 2013, 21, 6981-6995 Synthesis and biological evaluation of novel 1,6-diaryl pyridin-2(1H)-one analogs, European Journal of Medicinal Chemistry, 2013, 64, 613-620 The discovery of colchicine-SAHA hybrids as a new class of antitumor agents, Bioorganic & Medicinal Chemistry, 2013, 21, 3240-3244. Evolution in medicinal chemistry of E-ring-modified Camptothecin analogs as anticancer agents, European Journal of Medicinal Chemistry, 2013, 63, 746-757 Synthesis and biological evaluation of new homocamptothecin analogs, European Journal of Medicinal Chemistry, 2012, 54, 417-422. Total Synthesis of Camptothecin and SN-38, The Journal of Organic Chemistry, 2012, 77(1), 713-717 Synthesis and Biological Evaluation of Piper Amide Analogues as HDAC Inhibitors, Bioorganic & Medicinal Chemistry Letters,2011, 21, 4844-4866 Design and synthesis of novel benzimidazole derivatives as inhibitors, Bioorganic & Medicinal Chemistry, 2010, 18, 5048-5055. Chimmitecan, a novel 9-substituted camptothecin, with improved anticancer pharmacologic profiles in vitro and in vivo, Clinic Cancer Research, 2007, 13, 1298-1237. Identification of 1-isopropylsulfonyl-2-amine benzimidazoles as a new class of inhibitors of hepatitis B virus, European Journal of Medicinal Chemistry, 2007, 42, 1358-1364. Synthesis and anti-hepatitis B virus activity of novel benzimidazole derivatives, Journal of Medicinal Chemistry, 2006, 49, 4790-4794. Synthesis and antitumor activity of the hexacyclic camptothecin derivatives, Bioorganic & Medicinal Chemistry Letters,2005, 15, 3233-3236. Synthesis and antitumor activity of 7-ethyl-9-alkyl derivatives of Camptothecin, Bioorganic & Medicinal Chemistry Letters,2005, 15, 2003-2006.

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