- 单位:文华学院 城市建设工程学部
- 职称:教授
- 职位:教师
- 出生:1986.7
- 性别:女
- 社会职务: 无
研究领域
分子生物学,生物化学
论文与著作
Wang C, LuoY, Tang H, Yan Y, Chang X, Zhao R, Li Q, Yang P, Hong B, Xu Y, Huang Q*, Liu J*. Hsa_circ_0031608:A Potential Modulator of VSMC Phenotype in the Rupture of Intracranial Aneurysms. Frontiers in Molecular Neuroscience. 2022, doi:10.3389/fnmol.2022.842865.
Luo Y, Yang Y, HouW*, Fu J*. Novel Algicides against Bloom-FormingCyanobacteria from Allelochemicals: Design, Synthesis, Bioassay, and 3D-QSARStudy. Biology. 2021, 10, 1145.
Luo Y, Tang H,Zhang Z, Zhao R, Hou W*, Huang Q, LiuJ*. Pharmacological inhibition of epidermal growth factor receptor attenuates intracranial aneurysm formation by modulating the phenotype of vascular smooth muscle cells. CNSNeuroscience & Therapeutics. 2022, 28, 64-76.
Luo Y, Wang Y, FuJ*. Nanomaterials in Cerebro vascular Disease Diagnose and Treatment. Particle & Particle SystemsCharacterization. 2021, 38, 2000311.
Li H†, Luo Y†, LiuP, Liu P, Hua W, Zhang Y, Zhang L, Li Z, Xing P, Zhang Y, Hong B, Yang P*, Liu J*.Exosomes containingmiR-451a is involved in the protective effect of cerebral ischemicpreconditioning against cerebral ischemia and reperfusion injury. CNS Neuroscience & Therapeutics. 2021, 27,564-576.
Li H†, Luo Y†, Zhu L, Hua W, Zhang Y, Zhang H, Zhang L, Li Z, Xing P, Zhang Y, Hong B,Yang P*,Liu J*. Glia-derivedexosomes: Promising therapeutic targets. Life Sciences. 2019, 239,116951.
Tang H†, Luo Y†, Zuo Q†, Wang C,Huang Q, Zhao R*, Liu J*. Current Understanding of the Molecular Mechanismbetween Hemodynamic-Induced Intracranial Aneurysm and Inflammation. CurrentProtein and Peptide Science. 2019, 20, 1-10.
Chen G,Luo Y, Warncke K, Sun Y, Yu D, Fu H, Behera M, Ramalingam S, Doetsch P, Lammers M,Curran W, Deng X*. Acetylationregulates ribonucleotide reductase activity and cancer cell growth. Nature Communications. 2019, 10, Article number: 3213.
Li H†, Luo Y†, Yang P*, Liu J*. Hydrogen as a complementary therapy against ischemic stroke: Areview of the evidence. Journal of the NeurologicalSciences. 2019, 396, 240-246.
Luo Y†,*, Tang H†, Li H†, Zhao R, Huang Q*, Liu J*. Recent advances in the development of neuroprotective agents and therapeutictargets in the treatment of cerebral ischemia. Eur. J. Med. Chem. 2019, 162,132-146
李翯,骆银,杨鹏飞,刘建民. 缺血性脑卒中神经保护治疗的研究进展. 第二军医大学学报,2018, 39,1040-1046.
Luo Y†, Zhou Y†, Song Y, ChenG, Wang Y. X., Tian Y, Fan W. W., Yang Y. S., Cheng T, Zhu H. L*. Optimization of Substituted Cinnamic Acyl Sulfonamide Derivatives as Tubulin Polymerization Inhibitors with Anticancer Activity. Bioorg. Chem. Lett, 2018, DOI: 10.1016/j.bmcl.2018.10.037.
Mo XL, Luo Y, Ivanov AA, Su R, Havel JJ, Li Z, Khuri F, Du Y*, Fu H*. Enabling systematic interrogation of protein-protein inter actions in live cells with a versatile ultra-high-throughput biosensor platform. J. Mol. Cell Bio. 2016, 8, 271-281.
Luo Y†, Liu Z. J.†, Shi J, Li J. R., Zhu H. L.* 1,3,4-Oxadiazole derivatives as potential antitumoragents: discovery, optimization and biological activity evaluation. Med.Chem. Commun., 2016, 7(2),263-271.
Zhou Y†, Luo Y†, Yang Y. S., Lu L, Zhu H. L.* Study of acylhydrazone derivatives with deoxygenated seven-membered ringsas potential beta-ketoacyl-acyl carrier protein synthase III (FabH) inhibitors.Med.Chem. Commun., 2016, 7(10), 1980-1987.
Luo Y.†, Zhou Y.†, Fu J., Zhu H. L.*4,5-Dihydropyrazole derivatives containing oxygen-bearing heterocycles aspotential telomerase inhibitors with anticancer activity. RSC ADVANCES, 2014, 4(45), 23904-23913.
Zhang S†., Luo Y†., He L. Q., Liu Z. J., Jiang A. Q., Yang Y. H., ZhuH. L.* Synthesis,biological evaluation, and molecular docking studies of novel 1,3,4-oxadiazolederivatives possessing benzotriazole moiety as FAK inhibitors with anticanceractivity. Bioorganic & Medicinal Chemistry,2013,21, 3723-3729.
Luo Y.†, Zhang S.†, Liu Z. J., Fu J.* Synthesis and antimicrobical evalution of a novel class of 1,3,4-thiadiazole: derivatives bearing 1,2,4-triazolo[1,5-a] pyrimidine moiety.European Journal of Medicinal Chemistry, 2013, 64, 54-61.
Luo Y.†, Zhang S.†, Qiu K. M., Zhu H. L.* Synthesis, biological evaluation, 3D-QSAR studies of novel aryl-2H-pyrazolederivatives as telomerase inhibitors.Bioorganic & Medicinal Chemistry Letter,2013, 23, 1091-1095.
Luo Y. †, Yang Y. S. †, Fu J., ZhuH. L.* Novel FabH inhibitors:a patent and article literature review (2000-2012). Expert Opinion on Therapeutic Patents, 2012, 22,1325-1336.
Luo Y. †, Zhang L. R.†, Hu Y.,Zhang S., Fu J., Wang X. M., Zhu H. L.* Synthesis and Antimicrobial Activities of OximesDerived from O-Benzylhydroxylamine as FabH Inhibitors. ChemMedChem, 2012, 7, 1587 -1593.
Li Y†.,Luo Y†., Hu Y., Zhu D.D., Zhang S., Liu Z. J., Gong H. B., Zhu H. L.* Design, synthesis and antimicrobial activities ofnitroimidazole derivatives containing 1,3,4-oxadiazole scaffold as FabH inhibitors.Bioorganic & Medicinal Chemistry,2012, 20, 4316-4322.
Luo Y. †, Song R. †, Li Y., ZhangS., Liu Z. J., Fu J., Zhu H. L.* Design,synthesis, and biological evaluation of chalcone oxime derivatives as potentialimmunosuppressive agents. Bioorganic & Medicinal Chemistry Letters, 2012, 22, 3039-3043.
Li H. Q., Luo Y., Qiao C. H. The Mechanisms ofAnticancer Agents by Genistein and Synthetic Derivatives of Isoflavone. Mini-Reviews in Medicinal Chemistry,2012, 12, 350-362.
Luo Y., Li Y., Qiu K. M., Lu X., Fu J., Zhu H. L.Metronidazole acid acyl sulfonamide: A novel class of anticancer agents andpotential EGFR tyrosine kinase inhibitors.Bioorganic & Medicinal Chemistry, 2011, 19, 6069-6076.
Luo Y., Qiu K. M., Lu X., Liu K., Fu J., Zhu H. L.Synthesis, biological evaluation, and molecular modeling of cinnamic acylsulfonamide derivatives as novel antitubulin agents. Bioorganic & Medicinal Chemistry, 2011, 19, 4730-4738.
Li H. Q., Luo Y., Zhu H. L. Discovery ofvinylogous carbamates as a novel class of β-ketoacyl-acyl carrier protein synthaseIII (FabH) inhibitors. Bioorganic &Medicinal Chemistry, 2011, 19, 4454-4459.
Luo Y., Li H. Q., Zhou Y., Li Z. L., Yan T., Zhu H. L.Metronidazole-Deoxybenzoin Derivatives as Anti-Helicobacter pylori Agents with Potent Inhibitory Activity againstHPE-Induced Interleukin-8. ChemMedChem,2010, 5, 1110 -1116.
Li H. Q.†, Luo Y. †, SongR., Li Z. L., Yan T., Zhu H. L. Design, Synthesis, and ImmunosuppressiveActivity of New Deoxybenzoin Derivatives. ChemMedChem,2010, 5, 1117-1122.
朱海亮,骆银,李环球.一种肟类化合物及其制备方法与用途,专利号:ZL 200910233389.3.
朱海亮,仇晓阳,李耀,骆银,刘芝珺. 一种查耳酮肟类化合物作为新型免疫抑制剂的制备方法与用途.专利号:ZL 201110351329.9.
朱海亮,骆银,王宇翔,田野,范未伟.一种含氧杂环的磺胺类衍生物在抗癌药物中的应用.专利号:ZL 201210122265.X.
朱海亮,李耀,骆银.恶二唑衍生物的合成及其在抗菌药物方面的应用.申请号:201210098367.2.
朱海亮,李耀,骆银.硝基咪唑衍生物的合成及其在抗菌药物方面的应用.申请号:201210098359.8.
朱海亮,张帅,骆银.一类含苯并三氮唑结构的1,3,4-恶二唑衍生物的制法与用途.申请号:201210499005.4.
张洪剑,杨鹏飞,赵瑞,骆银,赵普远,王川川,李嘉楠,冯明陶,唐海双.模拟血管壁受力作用的transwell细胞培养装置. 专利号:ZL 201810206947.6.
陈果,骆银.一种MCL-1抑制剂及其制备方法与应用.申请号:202011503260.2.
荣誉与奖励
1. 2023年,湖北省“楚天学者”。
2. 2023年,湖北省青年拔尖人才。
3. 2018年获长海医院“先进工作者”称号
4. 2013年获 南京大学“优秀毕业生”称号
5. 2012年获南京大学研究生国家奖学金
6. 2012年获南京大学优秀研究生奖学金
7. 2011年获南京大学赵安中奖学金
8. 2011年获 南京大学“优秀研究生”称号
9. 2010年获南京大学潘雪平助学金
10. 2009年获南京大学“化学生物学与药物设计”暑期学校学员一等奖
11. 2009年获南京大学优秀研究生奖学金
12. 2004年-2008年获南京大学西部开发助学工程奖