郭丽，女，毕业于四川医学院，德国Tuebingen大学有机化学研究所，博士后，现为四川大学华西药学院教授、博士生导师，华西药学院药物化学系主任。兼任四川省学术和技术带头人后备人选，四川省卫生厅学术和技术带头人，四川省新药评审委员、四川省科技计划项目评审专家。
研究方向：靶向药物及聚集型多肽药物的研究，树枝状化合物在药物研究中的应用，主要研究课题及成果有“新型多分枝状肽大分子的合成及初步生物活性的研究”等3项，代表论著有微波辅助合成罗库溴铵重要中间体等25项。
人物经历
教育经历
工作经历
1995年在四川大学化工学院晋升副教授。
2000年～2001年德国Tuebingen大学有机化学研究所,博士后工作。
2003年在四川大学华西药学院晋升教授,2004年聘为博士生导师。
2007～至今华西药学院药物化学系主任。
获得荣誉
先后获四川大学校级教学成果奖、卓越教学奖、优秀教师称号，连续多年获得校级及学院优秀教学奖励。
研究方向
1．靶向药物及聚集型多肽药物的研究。
2．树枝状化合物在药物研究中的应用。
社会任职
四川省学术和技术带头人后备人选，四川省卫生厅学术和技术带头人，四川大学教学名师培养对象。国家科技奖励评审专家，国家自然科学基金同行评审专家等。
主要成就
科研成就
先后负责国家自然科学基金项目2项，教育部归国人员科研启动基金项目1项，校级基金项目2项以及企业合作项目。主持多项国家级、省级以及校级教改项目。
研究成果
1.教育部留学回国人员启动基金项目“新型分子酶大分子的合成及初步生物活性的研究”、2003-2004,项目负责人；
2.国家自然科学基金项目“新型树状多聚活性肽化合物的合成及初步生物活性的研究”、2005-2007,项目负责人
3.四川大学振兴计划引进人才基金“酶法多肽及树状化合物合成研究”,2002-,项目负责人。
人才培养
已培养硕士及博士生研究生40余人。
个人作品
发表论文
（2012～）在国内外核心期刊上发表科研论文90多篇。
1.Novel Dendritic 萘普生 Prodrugs with Poly(aspartic acid) Oligopeptide: Synthesis and 羟基磷灰石 Binding In Vitro,Synthetic Communications,2012,42,3441-3451
2.Synthesis and preliminary evaluation of novel amphiphilic Janus dendrimers for bone-targeted drug delivery，Tetrahedron,2012,68,2943-2949
3.Synthesis, antibacterial activity and cytotoxicity of novel Janus peptide dendrimers, synlett，2012, 23,1937-1940
4.Dual-targeting delivery system for bone cancer: synthesis and preliminary biological evaluation, Drug Delivery，2012,19(7),317-326
5.Design and synthesis of novel Janus dendrimers as lipophilized antioxidants，synlett. 2013,24(8), 1011-1015
6.Dual-targeting Janus dendrimer based peptides for bone cancer: synthesis and preliminary biological evaluation, Letters in Organic 化学，2013,10(8),594-601
7.Design, synthesis and biological evaluation of enzymatically cleavable NSAIDs prodrugs derived from self-immolative dendritic scaffolds for the treatment of inflammatory diseases，Bioorganic Medicinal 化学，2013,21(14),4192-4200
8.Molecular Docking, QSAR and Molecular 动力学 Simulation on Spiro-oxindoles as MDM2 Inhibitors，Acta Chimica Sinica，2013,71,1396-1403
9.Multicomplex-Based Pharmacophore and QSAR of Aryl-sulfamides as Pyruvate Kinase M2 Activators, Acta Physico-Chimica Sinica,2013.29,1793-1803
10.Synthesis of cis or trans 4-heteroaromatic substituted 呋喃 and pyrano[3,2-c] tetra- hydroquinolines by onepot imino diels-alder reactions, Heterocycles, 2013, 87(12),2495- 2500
11.Synthesis and Intestinal Absorption Evaluation Of oligopeptide Prodrugs Based On PepT1, West China J.Pharm.Sci., 2013,28(3),223-225
12.Preparation and Characterization of Glycyrrhetinic Acid-Modified Poloxamer 188/Chitosan Nanoparticles. NANO: Brief Reports and Reviews, 2013, 8(4), 1350042-1-8
13.Cell-penetrable lysine dendrimers for anti-cancer drug delivery: synthesis and preliminary biological evaluation，Archiv der Pharmazie, 2014, 347, 469-477
14.Dimer and Tetramer of Gallic Acid: Facile Synthesis, Antioxidant and Antiproliferative Activities，Letters in Drug 设计 \u0026 Discovery, 2014, 11, 27-32
15.Diastereoselective，Three-component ，Reaction of Chiral Nickel(II)， Glycinate for Convenient Synthesis of Novel α-amino-β-substituted-γ,γ-disubstituted butyric Acid, Molecules,2014,19,826-845
16.Discovery and in vivo Evaluation of Novel RGD-Modified Lipid-Polymer Hybrid Nanoparticles for Targeted Drug Delivery, Int. J. 摩尔 Sci., 2014,15, 17565-17576
17.Design, synthesis and biological evaluation of brain targeting L-ascorbic acid prodrugs of ibuprofen with “lock-in” 函数, European Journal of Medicinal 化学, 2014,82,314-323
18.Efficient Synthesis of Substances Related to Cinacalcet Hydrochloride via Heck Coupling，Synthetic Communications，2014，44，2879-2885
19a novel and convenient route for the construction of 5-((1H-1,2,4-三唑1-yl)甲基) -1H-indoles and its application in the synthesis of Rizatriptan, Tetrahedron Letters, 2014,55,3938-3941
20.Preparation and characterization of glycyrrhetinic acid-modified poly(乙烯 glycol)-poly(β-benzyl-L-asparate) nanoparticles as liver- targeted delivery system, Colloid Polym Sci. ,2015,293,319-328
21.Synthesis and Preliminary Evaluation of Novel Bone-targeting NSAIDs Prodrugs based on Glutamic Acid Oligopeptides, Letters in Drug 设计 \u0026 Discovery, 2015, 12, 585-590
22.First synthesis of novel 3,30-bipyridazine derivatives as new potent antihepatocellular carcinoma agents, Tetrahedron, 2015, 71,7670-7675
23.First synthesis and characterization for the stereoisomers of Ulipristal acetate, Steroids ,2015,95,7-16
24.First synthesis and characterization of stereoisomers of choleretic drug dihydroxydibutylether, Chin. J. Chem. 2015, 33, 1145-1152
25.Novel 萘普生peptide-conjugated amphiphilic dendrimer self-assembly micelles for targeting Drug delivery to osteosarcoma cells，RSC Adv.,2016, 6,60327-60335
26.Efficient Synthesis of Fully Substituted Pyrrolidine-fused 3-Spirooxindoles via 1,3-Dipolar Cycloaddition of 氮丙环 and 3-Ylideneoxindole ,Molecules ,2016, 21,1113-1128
27.铜γ-cyclodextrin complexes immobilized on hexagonal boron nitride as an efficient catalyst in the multicomponent synthesis of 1,2,3-三唑，Journal of Catalysis，2016,344，286-292
28.First synthesis of 22-oxa-chenodeoxycholic acid analogue，Steroids， 2016,110,70-76
29.Report on the Synthesis of Isatins via Pyridinum Chlorochromate Catalyzed Intromolecular Cyclization Reactions,Synlett,2016,27,1292-1296
30.Ru(III)-mediated intramolecular ortho-C(sp2)-H activation/oxidative acylation: one-pot synthesis of isatins from α-hydroxy amides，Tetrahedron，2016，72，3193-3197
31.Synthesis Study on the Three Stereoisomers of 4-(3-Hydroxylbutoxy)-2-butanol, Chemical Journal of Chinese Universities-Chinese,2016,37,493-497
32.Synthesis and Preliminary Study of Indole Croconium as Photoacoustic Imaging Contrast Agent[J]. Chinese Journal of Synthetic 化学, 2017, 25(4): 287-290
33.Ligand-free C-C coupling reaction promoted by hexagonal boron nitride-supported 钯(II) catalyst in 液态水,Adv.Synth.Catal.,2017,359,454-466
编写教材
负责四川省精品课程《药物化学》，编写国家级规划教材《药物化学》、《有机化学》等。
参考资料
郭丽 教授(博士生导师).四川大学华西药学院.2021-12-12