Ying Yang

发表

Identification of natural products as selective PTP1B inhibitors via virtual screening.

Zhiyan Xiao, Ying Yang, Jinlong Tian, 2020, Bioorganic chemistry.

Design, synthesis and biological evaluation of dipeptides as novel non-covalent 20S proteasome inhibitors

Fang-fang Lai, Zhiyan Xiao, Xiao-guang Chen, 2021, Journal of Asian natural products research.

Optimization and biological evaluation of nicotinamide derivatives as Aurora kinase inhibitors.

Xingwei Xu, Huan He, Ying Yang, 2019, Bioorganic & medicinal chemistry.

Discovery of novel non-covalent inhibitors selective to the β5-subunit of the human 20S proteasome.

Li Huang, Chin-Ho Chen, Zhiyan Xiao, 2015, European journal of medicinal chemistry.

Design, synthesis and biological evaluation of triaryl compounds as novel 20S proteasome inhibitors.

Fang-fang Lai, Zhiyan Xiao, B. Wu, 2020, Bioorganic & medicinal chemistry letters.

Discovery of thiazolidin-4-one urea analogues as novel multikinase inhibitors that potently inhibit FLT3 and VEGFR2.

Yuting Zhou, Tao Chen, Xingwei Xu, 2019, Bioorganic & medicinal chemistry.

Synthesis and cytotoxicity of a novel series of saframycin-ecteinascidin analogs containing tetrahydro-β-carboline moieties.

Xiaoguang Chen, Zhiyan Xiao, Zhanzhu Liu, 2017, European journal of medicinal chemistry.

Integrated Approach to Identify Selective PTP1B Inhibitors Targeting the Allosteric Site

Lei Zhang, Ying Yang, Jinying Tian, 2021, J. Chem. Inf. Model..

Discovery of a semi-synthesized cyclolignan as a potent HIV-1 non-nucleoside reverse transcriptase inhibitor

C. Yao, Ying Guo, Ying Yang, 2019, Journal of Asian natural products research.

Design of novel N-phenylnicotinamides as selective cyclooxygenase-1 inhibitors.

Ying Yang, Lei Shi, Hailiang Zhu, 2011, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological evaluation of a series of novel GPR40 agonists containing nitrogen heterocyclic rings.

Z. Shen, Yi Huan, Zhiyan Xiao, 2018, Bioorganic & medicinal chemistry letters.

Design of novel nicotinamides as potent and selective monoamine oxidase a inhibitors.

Ying Yang, Lei Shi, Chan Liu, 2010, Bioorganic & medicinal chemistry.

Discovery of 1H-benzo[d][1,2,3]triazol-1-yl 3,4,5-trimethoxybenzoate as a potential antiproliferative agent by inhibiting histone deacetylase.

Jie Fu, Ying Yang, Xue-Wei Zhang, 2010, Bioorganic & medicinal chemistry.

Docking a bespoke ultra-large tetrahydropyridine library identifies 5-HT2A receptor agonists conferring new biology

Samuel T. Slocum, J. Irwin, B. Shoichet, 2022 .

Discovery of di-indolinone as a novel scaffold for protein tyrosine phosphatase 1B inhibitors.

Jia Li, Li-xin Gao, Ying Yang, 2012, Bioorganic & medicinal chemistry letters.

Bioactive neolignans and lignans from the bark of Machilus robusta.

Wei Cheng, Yan Li, Sheng Lin, 2011, Journal of natural products.

Design, synthesis, and structure-activity relationships of pyrazole derivatives as potential FabH inhibitors.

Yin Luo, Pengcheng Lv, Ying Yang, 2010, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological evaluation of quinoline amide derivatives as novel VEGFR-2 inhibitors.

Ying Yang, Lei Shi, Huan-qiu Li, 2010, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological evaluation of novel thiazole derivatives as potent FabH inhibitors.

Jin Chen, Pengcheng Lv, Ying Yang, 2009, Bioorganic & medicinal chemistry letters.

2,4,5-Trisubstituted thiazole derivatives as HIV-1 NNRTIs effective on both wild-type and mutant HIV-1 reverse transcriptase: Optimization of the substitution of positions 4 and 5.

Xiaoshan Huang, Ying Guo, Hua Zhou, 2016, European journal of medicinal chemistry.

Synthesis and antibacterial activities of copper(II) with [(2-hydroxy-3,5-diiodo-benzylidene)-amino]-acetic acid

Ying Yang, Lei Shi, Hailiang Zhu, 2010 .

Synthesis, molecular modeling and biological evaluation of dithiocarbamates as novel antitubulin agents.

Kui Cheng, Jing Zhao, Ying Yang, 2010, Bioorganic & medicinal chemistry.

Identification of xanthine oxidase inhibitors through hierarchical virtual screening

Zhiyan Xiao, Ying Yang, F. Ye, 2020, RSC advances.

Synthesis, characterization, and biological activity of a Schiff-base Zn(II) complex

Ying Yang, Wen-Jun Mao, Lei Shi, 2009 .

Design, synthesis and biological evaluation of thiazolidinone derivatives as potential EGFR and HER-2 kinase inhibitors.

Jin Chen, Changfang Zhou, Pengcheng Lv, 2010, Bioorganic & medicinal chemistry.

Identification of novel N1-(2-aryl-1, 3-thiazolidin-4-one)-N3-aryl ureas showing potent multi-tyrosine kinase inhibitory activities.

Yuting Zhou, Min Liu, Anmian Zhang, 2018, European journal of medicinal chemistry.

2,4,5-Trisubstituted thiazole derivatives: a novel and potent class of non-nucleoside inhibitors of wild type and mutant HIV-1 reverse transcriptase.

Ying Guo, Chaojun Tang, Ying Yang, 2014, European journal of medicinal chemistry.

Discovery of Novel N-Substituted Prolinamido Indazoles as Potent Rho Kinase Inhibitors and Vasorelaxation Agents

Tian-yi Yuan, L. Fang, Ping Xie, 2017, Molecules.

Synthesis, Crystal Structure and Immunosuppressive Activity of Acylamide Derivatives Containing 1,4‐Benzodioxan

Pengcheng Lv, Ying Yang, Wen-Jun Mao, 2009, ChemMedChem.

Identification of novel xanthine oxidase inhibitors via virtual screening with enhanced characterization of molybdopterin binding groups.

Lu Zhang, Zhiyan Xiao, Ying Yang, 2022, European journal of medicinal chemistry.

Ultraviolet irradiation combined with manganese ore catalyzed ozonation of 4-chlorophenol in aqueous solution.

S. An, Jie Fu, Ying Yang, 2010 .

Synthesis and structure-activity relationships of N-benzyl-N-(X-2-hydroxybenzyl)-N'-phenylureas and thioureas as antitumor agents.

Changfang Zhou, Ying Yang, Lei Shi, 2010, Bioorganic & medicinal chemistry.

Synthesis and antiproliferative activities against Hep-G2 of salicylanide derivatives: potent inhibitors of the epidermal growth factor receptor (EGFR) tyrosine kinase

Ying Yang, Lei Shi, Huan-qiu Li, 2011, Journal of enzyme inhibition and medicinal chemistry.

Discovery of N1-(4-((7-(3-(4-ethylpiperazin-1-yl)propoxy)-6-methoxyquinolin-4-yl)oxy)-3,5-difluorophenyl)-N3-(2-(2,6-difluorophenyl)-4-oxothiazolidin-3-yl)urea as a multi-tyrosine kinase inhibitor for drug-sensitive and drug-resistant cancers treatment.

Jun Yu Li, Tao Chen, Xingwei Xu, 2019, European journal of medicinal chemistry.

Synthesis and Biological Evaluation of 7-O-Modified Formononetin Derivatives

Pengcheng Lv, Ying Yang, Wen-Jun Mao, 2008 .

Synthesis and biological evaluation of acridine-based histone deacetylase inhibitors as multitarget agents against Alzheimer's disease.

S. Pan, Chih-Jou Su, Wei-Jan Huang, 2020, European journal of medicinal chemistry.

Design, synthesis and insulin-sensitising effects of novel PTP1B inhibitors.

Zhon-Yin Zhang, Chun Hu, Zhiyan Xiao, 2013, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological evaluation of exiguamine A analogues as IDO1 inhibitors.

Zhiyan Xiao, J. Dong, Guangyan Zhang, 2021, European journal of medicinal chemistry.

Design and synthesis of potent inhibitors of beta-ketoacyl-acyl carrier protein synthase III (FabH) as potential antibacterial agents.

Kui Cheng, W. Zhong, Ying Yang, 2010, European journal of medicinal chemistry.

Design of novel nicotinamides as potent and selective monoamine oxidase a inhibitors.

Ying Yang, Lei Shi, Chan Liu, 2010, Bioorganic & medicinal chemistry.