Zhiyu Li, Ph.D. - Publications

Institution:
Indiana University, Bloomington, Bloomington, IN, United States
Area:
Structure analysis of biological systems using mass spectrometry-based techniques

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Year Citation  Score
2015 Khanal N, Pejaver V, Li Z, Radivojac P, Clemmer DE, Mukhopadhyay S. Position of Proline Mediates the Reactivity of S-Palmitoylation. Acs Chemical Biology. PMID 26255674 DOI: 10.1021/Acschembio.5B00429  0.477
2014 Li Z, Dilger JM, Pejaver V, Smiley D, Arnold RJ, Mooney SD, Mukhopadhyay S, Radivojac P, Clemmer DE. Intrinsic Size Parameters for Palmitoylated and Carboxyamidomethylated Peptides. International Journal of Mass Spectrometry. 368: 6-14. PMID 26023288 DOI: 10.1016/J.Ijms.2014.04.009  0.483
2012 Lee S, Li Z, Valentine SJ, Zucker SM, Webber N, Reilly JP, Clemmer DE. Extracted Fragment Ion Mobility Distributions: A New Method for Complex Mixture Analysis. International Journal of Mass Spectrometry. 309: 154-160. PMID 22518092 DOI: 10.1016/J.Ijms.2011.09.011  0.593
2011 Li Z, Valentine SJ, Clemmer DE. Complexation of amino compounds by 18C6 improves selectivity by IMS-IMS-MS: application to petroleum characterization. Journal of the American Society For Mass Spectrometry. 22: 817-27. PMID 21472516 DOI: 10.1007/S13361-011-0105-0  0.593
Low-probability matches (unlikely to be authored by this person)
2017 Li Z, Kim J, Regnier FE. MOBILE AFFINITY SORBENT CHROMATOGRAPHY (MASC). Analytical Chemistry. PMID 29260867 DOI: 10.1021/Acs.Analchem.7B03117  0.271
2009 Quan L, Cao Q, Li Z, Li N, Li K, Liu F. Highly efficient and low-cost purification of lysozyme: a novel tris(hydroxymethyl)aminomethane immobilized affinity column. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences. 877: 594-8. PMID 19188100 DOI: 10.1016/J.Jchromb.2009.01.018  0.259
2008 Quan L, Wei D, Jiang X, Liu Y, Li Z, Li N, Li K, Liu F, Lai L. Resurveying the Tris buffer solution: the specific interaction between tris(hydroxymethyl)aminomethane and lysozyme. Analytical Biochemistry. 378: 144-50. PMID 18448066 DOI: 10.1016/J.Ab.2008.04.006  0.251
2009 Yang Y, Long Y, Li Z, Li N, Li K, Liu F. Real-time molecular recognition between protein and photosensitizer of photodynamic therapy by quartz crystal microbalance sensor. Analytical Biochemistry. 392: 22-7. PMID 19481051 DOI: 10.1016/J.Ab.2009.05.035  0.227
2013 Joshi MR, Yao N, Myers KA, Li Z. Human serum albumin and p53-activating peptide fusion protein is able to promote apoptosis and deliver fatty acid-modified molecules. Plos One. 8: e80926. PMID 24278348 DOI: 10.1371/Journal.Pone.0080926  0.189
2013 Kong Y, Shao Y, Chen H, Ming X, Wang JB, Li ZY, Wei JF. A Novel Factor Xa-Inhibiting Peptide from Centipedes Venom. International Journal of Peptide Research and Therapeutics. 19: 303-311. PMID 24273471 DOI: 10.1007/S10989-013-9353-0  0.189
2023 Shi RL, Dillon MA, Compton PD, Sawyer WS, Thorup JR, Kwong M, Chan P, Chiu CPC, Li R, Yadav R, Lee GY, Gober JG, Li Z, ElSohly AM, Ovacik AM, et al. High-Throughput Analyses of Therapeutic Antibodies Using High-Field Asymmetric Waveform Ion Mobility Spectrometry Combined with SampleStream and Intact Protein Mass Spectrometry. Analytical Chemistry. PMID 37956201 DOI: 10.1021/acs.analchem.3c03158  0.182
2018 Bian J, Ren J, Li Y, Wang J, Xu X, Feng Y, Tang H, Wang Y, Li Z. Discovery of Wogonin-based PROTACs against CDK9 and capable of achieving antitumor activity. Bioorganic Chemistry. 81: 373-381. PMID 30196207 DOI: 10.1016/j.bioorg.2018.08.028  0.168
2014 Luo R, Wang J, Zhao L, Lu N, You Q, Guo Q, Li Z. Synthesis and biological evaluation of baicalein derivatives as potent antitumor agents. Bioorganic & Medicinal Chemistry Letters. 24: 1334-8. PMID 24507925 DOI: 10.1016/j.bmcl.2014.01.053  0.167
2022 Xu X, Zhang D, Zhao T, Wang M, Li Y, Du Q, Kou J, Li Z, Bian J. Novel biphenyl-based scaffold as potent and selective histone deacetylase 6 (HDAC6) inhibitors: Identification, development and pharmacological evaluation. European Journal of Medicinal Chemistry. 233: 114228. PMID 35245830 DOI: 10.1016/j.ejmech.2022.114228  0.167
2008 Li Z, Zhai F, Zhao L, Guo Q, You Q. Design and synthesis of N-methylmaleimide indolocarbazole bearing modified 2-acetamino acid moieties as Topoisomerase I inhibitors. Bioorganic & Medicinal Chemistry Letters. 19: 406-9. PMID 19058964 DOI: 10.1016/j.bmcl.2008.11.061  0.165
2012 Xia Y, Wu C, Liu W, Feng F, Li Z. A novel process related impurity and forced degradation study of synthetic wogonin: development of a liquid chromatographic method for purity control. Journal of Pharmaceutical and Biomedical Analysis. 71: 168-72. PMID 22906689 DOI: 10.1016/j.jpba.2012.07.030  0.163
2019 Wang J, Li T, Zhao T, Wu T, Liu C, Ding H, Li Z, Bian J. Design of wogonin-inspired selective cyclin-dependent kinase 9 (CDK9) inhibitors with potent in vitro and in vivo antitumor activity. European Journal of Medicinal Chemistry. 178: 782-801. PMID 31238183 DOI: 10.1016/j.ejmech.2019.06.024  0.163
2017 Wang J, Ge R, Qiu X, Xu X, Wei L, Li Z, Bian J. Discovery and synthesis of novel Wogonin derivatives with potent antitumor activity in vitro. European Journal of Medicinal Chemistry. 140: 421-434. PMID 28987604 DOI: 10.1016/j.ejmech.2017.09.046  0.162
2016 Lu Y, Yang D, Li Z, Hang T, Song M. Isolation and characterization of related substances in alogliptin benzoate by LC-QTOF mass spectrometric techniques. Journal of Pharmaceutical and Biomedical Analysis. 128: 253-263. PMID 27281581 DOI: 10.1016/j.jpba.2016.04.032  0.156
2011 Liu W, Zhou J, Qi F, Bensdorf K, Li Z, Zhang H, Qian H, Huang W, Cai X, Cao P, Wellner A, Gust R. Synthesis and biological activities of 2-amino-thiazole-5-carboxylic acid phenylamide derivatives. Archiv Der Pharmazie. 344: 451-8. PMID 21598297 DOI: 10.1002/Ardp.201000281  0.156
2014 Kong Y, Xu C, He ZL, Zhou QM, Wang JB, Li ZY, Ming X. A novel peptide inhibitor of platelet aggregation from stiff silkworm, Bombyx batryticatus. Peptides. 53: 70-8. PMID 24361453 DOI: 10.1016/J.Peptides.2013.12.004  0.156
2009 You QD, Li ZY, Huang CH, Yang Q, Wang XJ, Guo QL, Chen XG, He XG, Li TK, Chern JW. Discovery of a novel series of quinolone and naphthyridine derivatives as potential topoisomerase I inhibitors by scaffold modification. Journal of Medicinal Chemistry. 52: 5649-61. PMID 19715319 DOI: 10.1021/jm900469e  0.155
2009 Li ZY, Lu PB, Ji H, Shao Q, You QD, Liu X. [Synthesis and anti-histamine release activity of phenyl tetrazole compounds]. Yao Xue Xue Bao = Acta Pharmaceutica Sinica. 44: 1112-7. PMID 20055133  0.155
2019 Han JP, Zhu ZH, Wu YZ, Qian W, Li ZY, Nishikawa M, Sakaki T, Yang CQ. Preparation of a Major Metabolite of Iguratimod and Simultaneous Assay of Iguratimod and Its Metabolite by HPLC in Rat Plasma. Iranian Journal of Pharmaceutical Research : Ijpr. 18: 631-641. PMID 31531047 DOI: 10.22037/ijpr.2019.1100641  0.153
2022 Mao D, Hong L, Fu L, Li Z, Chen J, Zhang C, Wu Y, Xiong W, Wang J. Authenticity Assessment of (E)-Cinnamic Acid, Vanillin, and Benzoic Acid from Sumatra Benzoin Balsam by Gas Chromatography Combustion/Pyrolysis Isotope Ratio Mass Spectrometry. International Journal of Analytical Chemistry. 2022: 1747053. PMID 36118270 DOI: 10.1155/2022/1747053  0.152
2012 Liu B, You QD, Li ZY. [Synthesis and biological evaluation of 3-quinolinecarbonitrile-7-amide derivatives]. Yao Xue Xue Bao = Acta Pharmaceutica Sinica. 44: 879-84. PMID 20055156  0.151
2024 Qin L, Cheng X, Wang S, Gong G, Su H, Huang H, Chen T, Damdinjav D, Dorjsuren B, Li Z, Qiu Z, Bian J. Discovery of Novel Aminobutanoic Acid-Based ASCT2 Inhibitors for the Treatment of Non-Small-Cell Lung Cancer. Journal of Medicinal Chemistry. PMID 38217503 DOI: 10.1021/acs.jmedchem.3c01093  0.151
2023 Li P, Tian Y, Shang Q, Tang C, Hou Z, Li Y, Cao L, Xue S, Bian J, Luo C, Wu D, Li Z, Ding H. Discovery of a highly potent NPAS3 heterodimer inhibitor by covalently modifying ARNT. Bioorganic Chemistry. 139: 106676. PMID 37352720 DOI: 10.1016/j.bioorg.2023.106676  0.151
2022 Xu X, Chang X, Huang J, Zhang D, Wang M, Jing T, Zhuang Y, Kou J, Qiu Z, Wang J, Li Z, Bian J. Discovery of novel glutaminase 1 allosteric inhibitor with 4-piperidinamine linker and aromatic heterocycles. European Journal of Medicinal Chemistry. 236: 114337. PMID 35428013 DOI: 10.1016/j.ejmech.2022.114337  0.15
2020 Li Z, Wang J, Zheng B, Guo Z. Impact of combined ultrasound-microwave treatment on structural and functional properties of golden threadfin bream (Nemipterus virgatus) myofibrillar proteins and hydrolysates. Ultrasonics Sonochemistry. 65: 105063. PMID 32199256 DOI: 10.1016/j.ultsonch.2020.105063  0.15
2022 Ren J, Quan X, Liu Y, Li J, Zhang X, Li Z, Zhang X. Synthesis and in vitro biological evaluation of 3-ethyl-1,5-naphthyridin-2(1H)-one derivatives as potent PARP-1 selective inhibitors and PARP-1 DNA trappers. Bioorganic & Medicinal Chemistry Letters. 129046. PMID 36343904 DOI: 10.1016/j.bmcl.2022.129046  0.15
2019 Zhong Y, Meng Y, Xu X, Zhao L, Li Z, You Q, Bian J. Design, synthesis and evaluation of phthalazinone thiohydantoin-based derivative as potent PARP-1 inhibitors. Bioorganic Chemistry. 91: 103181. PMID 31404795 DOI: 10.1016/j.bioorg.2019.103181  0.149
2019 Xu X, Kuang Z, Han J, Meng Y, Li L, Luan H, Xu P, Wang J, Luo C, Ding H, Li Z, Bian J. Development and Characterization of a Fluorescent Probe for GLS1 and the Application for High-Throughput Screening of Allosteric Inhibitors. Journal of Medicinal Chemistry. PMID 31603674 DOI: 10.1021/acs.jmedchem.9b01035  0.149
2019 Du Q, Feng X, Wang Y, Xu X, Zhang Y, Qu X, Li Z, Bian J. Discovery of phosphonamidate IDO1 inhibitors for the treatment of non-small cell lung cancer. European Journal of Medicinal Chemistry. 182: 111629. PMID 31445231 DOI: 10.1016/j.ejmech.2019.111629  0.148
2019 Feng X, Shen P, Wang Y, Li Z, Bian J. Synthesis and in vivo antitumor evaluation of an orally active potent phosphonamidate derivative targeting IDO1/IDO2/TDO. Biochemical Pharmacology. PMID 31306643 DOI: 10.1016/j.bcp.2019.07.011  0.147
2016 Zuo M, Xu X, Xie Z, Ge R, Zhang Z, Li Z, Bian J. Design and synthesis of indoline thiohydantoin derivatives based on enzalutamide as antiproliferative agents against prostate cancer. European Journal of Medicinal Chemistry. 125: 1002-1022. PMID 27810589 DOI: 10.1016/j.ejmech.2016.10.049  0.146
2008 Cao X, You QD, Li ZY, Liu XR, Xu D, Guo QL, Shang J, Chern JW, Chen ML. The design, synthesis and biological evaluation of 7-alkoxy-4-heteroarylamino-3-cyanoquinolines as dual inhibitors of c-Src and iNOS. Bioorganic & Medicinal Chemistry Letters. 18: 6206-9. PMID 18930653 DOI: 10.1016/j.bmcl.2008.10.006  0.146
2024 Li Z, Zhong X, Luan C, Wen N, Shi C, Lin X, Zhao C, Zhang Y, Luo L, Zhang L, Wu Y, Yang J. Fabrication of high-preformance emulsifier from conjugating maltodextrin onto myofibrillar protein peptide with microwave- ultrasound synergy. Ultrasonics Sonochemistry. 104: 106818. PMID 38452710 DOI: 10.1016/j.ultsonch.2024.106818  0.145
2016 Ge R, Zhao Q, Xie Z, Lu L, Guo Q, Li Z, Zhao L. Synthesis and biological evaluation of 6-fluoro-3-phenyl-7-piperazinyl quinolone derivatives as potential topoisomerase I inhibitors. European Journal of Medicinal Chemistry. 122: 465-474. PMID 27416553 DOI: 10.1016/j.ejmech.2016.06.054  0.145
2014 Hui H, Chen Y, Yang H, Zhao K, Wang Q, Zhao L, Wang X, Li Z, Lu N, Guo Q. Oroxylin A has therapeutic potential in acute myelogenous leukemia by dual effects targeting PPARγ and RXRα. International Journal of Cancer. Journal International Du Cancer. 134: 1195-206. PMID 23934681 DOI: 10.1002/Ijc.28435  0.145
2009 Cao X, You QD, Li ZY, Guo QL, Yang Y, Shang J, Yan M, Chen JW, Chen ML. [The design, synthesis and anticancer activity of 4-heteroarylamino-3-cyanoquinolines as dual inhibitors of c-Src and iNOS]. Yao Xue Xue Bao = Acta Pharmaceutica Sinica. 44: 288-95. PMID 19449526  0.145
2022 Chang X, Wang M, Zhang D, Zhang Y, Wang J, Li Z, Bian J, Xu X. Design, synthesis, and biological evaluation of novel glutaminase 1 allosteric inhibitors with an alkane chain tail group. European Journal of Medicinal Chemistry. 246: 115014. PMID 36525694 DOI: 10.1016/j.ejmech.2022.115014  0.144
2016 Xia QH, Hu W, Li C, Wu JF, Yang L, Han XM, Shen YM, Li ZY, Li X. Design, synthesis, biological evaluation and molecular docking study on peptidomimetic analogues of XK469. European Journal of Medicinal Chemistry. 124: 311-325. PMID 27597408 DOI: 10.1016/j.ejmech.2016.08.010  0.143
2003 Woodard CL, Li Z, Kathcart AK, Terrell J, Gerena L, Lopez-Sanchez M, Kyle DE, Bhattacharjee AK, Nichols DA, Ellis W, Prigge ST, Geyer JA, Waters NC. Oxindole-based compounds are selective inhibitors of Plasmodium falciparum cyclin dependent protein kinases. Journal of Medicinal Chemistry. 46: 3877-82. PMID 12930149 DOI: 10.1021/jm0300983  0.143
2023 Wu T, Zhang Z, Gong G, Du Z, Xu Y, Yu S, Ma F, Zhang X, Wang Y, Chen H, Wu S, Xu X, Qiu Z, Li Z, Wu H, et al. Discovery of novel flavonoid-based CDK9 degraders for prostate cancer treatment via a PROTAC strategy. European Journal of Medicinal Chemistry. 260: 115774. PMID 37672930 DOI: 10.1016/j.ejmech.2023.115774  0.142
2017 Bian J, Li T, Weng T, Wang J, Chen Y, Li Z. Synthesis, evaluation and quantitative structure-activity relationship (QSAR) analysis of Wogonin derivatives as cytotoxic agents. Bioorganic & Medicinal Chemistry Letters. PMID 28117202 DOI: 10.1016/j.bmcl.2016.12.076  0.142
2008 Cao X, You QD, Li ZY, Guo QL, Shang J, Yan M, Chern JW, Chen ML. Design and synthesis of 7-alkoxy-4-heteroarylamino-3-quinolinecarbonitriles as dual inhibitors of c-Src kinase and nitric oxide synthase Bioorganic and Medicinal Chemistry. 16: 5890-5898. PMID 18485715 DOI: 10.1016/j.bmc.2008.04.065  0.141
2022 Tian Y, Liu K, Liu R, Qiu Z, Xu Y, Wei W, Xu X, Wang J, Ding H, Li Z, Bian J. Discovery of Potent Small-Molecule USP8 Inhibitors for the Treatment of Breast Cancer through Regulating ERα Expression. Journal of Medicinal Chemistry. PMID 35786929 DOI: 10.1021/acs.jmedchem.2c00013  0.141
2012 Qin Y, Li Z, Chen Y, Hui H, Sun Y, Yang H, Lu N, Guo Q. III-10, a newly synthesized flavonoid, induced differentiation of human U937 leukemia cells via PKCδ activation. European Journal of Pharmaceutical Sciences : Official Journal of the European Federation For Pharmaceutical Sciences. 45: 648-56. PMID 22266210 DOI: 10.1016/j.ejps.2012.01.004  0.141
2012 Zhang X, Wang R, Zhao L, Lu N, Wang J, You Q, Li Z, Guo Q. Synthesis and biological evaluations of novel indenoisoquinolines as topoisomerase I inhibitors. Bioorganic & Medicinal Chemistry Letters. 22: 1276-81. PMID 22079759 DOI: 10.1016/j.bmcl.2011.10.019  0.14
2012 Hu R, Chen N, Yao J, Zhao Q, Zhang F, Li ZY, You QD, Guo QL. The role of Nrf2 and apoptotic signaling pathways in oroxylin A-mediated responses in HCT-116 colorectal adenocarcinoma cells and xenograft tumors Anti-Cancer Drugs. 23: 651-658. PMID 22526619 DOI: 10.1097/CAD.0b013e3283512703  0.14
2018 Roscoe I, Parker M, Dong D, Li X, Li Z. Human serum albumin and p53-derived peptide fusion protein promotes cytotoxicity irrespective of p53 status in cancer cells. Molecular Pharmaceutics. PMID 30226785 DOI: 10.1021/acs.molpharmaceut.8b00647  0.139
2019 Xu X, Ren J, Ma Y, Liu H, Rong Q, Feng Y, Wang Y, Cheng Y, Ge R, Li Z, Bian J. Discovery of cyanopyridine scaffold as novel indoleamine-2,3-dioxygenase 1 (IDO1) inhibitors through virtual screening and preliminary hit optimisation. Journal of Enzyme Inhibition and Medicinal Chemistry. 34: 250-263. PMID 30734612 DOI: 10.1080/14756366.2018.1480614  0.139
2019 Redij T, Chaudhari R, Li Z, Hua X, Li Z. Structural Modeling and in Silico Screening of Potential Small-Molecule Allosteric Agonists of a Glucagon-like Peptide 1 Receptor. Acs Omega. 4: 961-970. PMID 31459371 DOI: 10.1021/acsomega.8b03052  0.138
2018 Li H, Lu N, Yu X, Liu X, Hu P, Zhu Y, Shen L, Xu J, Li Z, Guo Q, Hui H. Oroxylin A,a natural compound, mitigates the negative effects of TNFα-treated acute myelogenous leukemia cells. Carcinogenesis. PMID 29346508 DOI: 10.1093/carcin/bgy004  0.138
2020 Fu Y, Wang Z, Zhang Q, Li Z, Liu H, Bi X, Wang J. Ru(ii)-catalyzed C6-selective C-H acylmethylation of pyridones using sulfoxonium ylides as carbene precursors. Rsc Advances. 10: 6351-6355. PMID 35496007 DOI: 10.1039/c9ra10749e  0.137
2013 Xu X, Liu F, Zhang S, Jia J, Li Z, Guo X, Yang Y, Sun H, You Q. Indenoisoquinoline derivatives as topoisomerase I inhibitors that suppress angiogenesis by affecting the HIF signaling pathway. Biomedicine & Pharmacotherapy = BioméDecine & PharmacothéRapie. 67: 715-22. PMID 23932721 DOI: 10.1016/j.biopha.2013.06.004  0.137
2015 Xie Z, Cao C, Feng S, Huang J, Li Z. Progress in the research of GPIIb/IIIa antagonists. Future Medicinal Chemistry. 7: 1149-1171. PMID 26132524 DOI: 10.4155/fmc.15.53  0.137
2015 Xie Z, Zhou Y, Zhao W, Jiao H, Chen Y, Yang Y, Li Z. Identification of novel PARP-1 inhibitors: Drug design, synthesis and biological evaluation. Bioorganic & Medicinal Chemistry Letters. PMID 26342868 DOI: 10.1016/j.bmcl.2015.08.060  0.136
2022 Redij T, McKee JA, Do P, Campbell JA, Ma J, Li Z, Miller N, Srikanlaya C, Zhang D, Hua X, Li Z. 2-Aminothiophene Derivatives as a New Class of Positive Allosteric Modulators of Glucagon-Like Peptide 1 Receptor. Chemical Biology & Drug Design. PMID 35313084 DOI: 10.1111/cbdd.14039  0.136
2011 Yang Z, Qiang L, Wu T, Chen FH, Yang HY, Zhao Q, Zou MJ, Sun YJ, Li ZY, Guo QL. Reactive oxygen species-mitochondria pathway involved in FV-429-induced apoptosis in human hepatocellular carcinoma HepG2 cells. Anti-Cancer Drugs. 22: 886-95. PMID 21730822 DOI: 10.1097/CAD.0b013e3283483d65  0.135
2014 Zhang Y, Zhao L, Li X, Wang Y, Yao J, Wang H, Li F, Li Z, Guo Q. V8, a newly synthetic flavonoid, induces apoptosis through ROS-mediated ER stress pathway in hepatocellular carcinoma. Archives of Toxicology. 88: 97-107. PMID 23835921 DOI: 10.1007/s00204-013-1085-6  0.135
2021 Yuan K, Ji M, Xie S, Qiu Z, Chen W, Min W, Xia F, Zheng M, Wang X, Li J, Hou Y, Kuang W, Wang L, Gu W, Li Z, et al. Discovery of Dual CDK6/PIM1 Inhibitors with a Novel Structure, High Potency, and Favorable Druggability for the Treatment of Acute Myeloid Leukemia. Journal of Medicinal Chemistry. PMID 34958208 DOI: 10.1021/acs.jmedchem.1c02019  0.135
2017 Xu X, Ge R, Li L, Wang J, Lu X, Xue S, Chen X, Li Z, Bian J. Exploring the tetrahydroisoquinoline thiohydantoin scaffold blockade the androgen receptor as potent anti-prostate cancer agents. European Journal of Medicinal Chemistry. PMID 29117897 DOI: 10.1016/j.ejmech.2017.10.031  0.135
2023 Wu T, Yu B, Gong W, Zhang J, Yu S, Tian Y, Zhao T, Li Z, Wang J, Bian J. Design and optimization of selective and potent CDK9 inhibitors with flavonoid scaffold for the treatment of acute myeloid leukemia. European Journal of Medicinal Chemistry. 259: 115711. PMID 37572539 DOI: 10.1016/j.ejmech.2023.115711  0.133
2015 Sun J, Li F, Zhao Y, Zhao L, Qiao C, Li Z, Guo Q, Lu N. LZ-207, a Newly Synthesized Flavonoid, Induces Apoptosis and Suppresses Inflammation-Related Colon Cancer by Inhibiting the NF-κB Signaling Pathway. Plos One. 10: e0127282. PMID 26023926 DOI: 10.1371/journal.pone.0127282  0.133
2020 Zou X, Meng F, Fu C, Zhou J, Zhang Y, Wang R, Zhang C, Li Z, Guo Q, Yang L. LZ-106, a potent lysosomotropic agent, causing TFEB-dependent cytoplasmic vacuolization. Gene. 145017. PMID 32755655 DOI: 10.1016/j.gene.2020.145017  0.132
2012 Fu W, Wang J, Yu L, Zhao L, Lu N, You Q, Guo Q, Li Z. Synthesis and biological evaluation of 7-O-modified oroxylin A derivatives. Bioorganic & Medicinal Chemistry Letters. 22: 1118-21. PMID 22196122 DOI: 10.1016/j.bmcl.2011.11.117  0.132
2016 Li T, Weng T, Zuo M, Wei Z, Chen M, Li Z. Recent progress of cyclin-dependent kinase inhibitors as potential anticancer agents. Future Medicinal Chemistry. PMID 27774795 DOI: 10.4155/fmc-2016-0129  0.132
2023 Li Z, Lin L, Fu G, Guo Z, Zhang C. Insight on the emulsifying mechanisms of low-salt type emulsions stabilized by Maillard conjugates: Myofibrillar protein peptide-dextrin with different degrees of hydrolysis. Food Chemistry. 137151. PMID 37661502 DOI: 10.1016/j.foodchem.2023.137151  0.132
2009 Zeng S, Liu W, Nie FF, Zhao Q, Rong JJ, Wang J, Tao L, Qi Q, Lu N, Li ZY, Guo QL. LYG-202, a new flavonoid with a piperazine substitution, shows antitumor effects in vivo and in vitro. Biochemical and Biophysical Research Communications. 385: 551-6. PMID 19481059 DOI: 10.1016/j.bbrc.2009.05.099  0.131
2021 Li ZY, Azi F, Dong JJ, Liu LZ, Ge ZW, Dong MS. Green and efficient in-situ biosynthesis of antioxidant and antibacterial bacterial cellulose using wine pomace. International Journal of Biological Macromolecules. 193: 2183-2191. PMID 34785197 DOI: 10.1016/j.ijbiomac.2021.11.049  0.131
2024 Sun X, Li Z, Wang X, He J, Wu Y. Inorganic Phosphate as "Bioenergetic Messenger" Triggers M2-Type Macrophage Polarization. Advanced Science (Weinheim, Baden-Wurttemberg, Germany). e2306062. PMID 38247159 DOI: 10.1002/advs.202306062  0.13
2020 Qiu X, Li Y, Yu B, Ren J, Huang H, Wang M, Ding H, Li Z, Wang J, Bian J. Discovery of selective CDK9 degraders with enhancing antiproliferative activity through PROTAC conversion. European Journal of Medicinal Chemistry. 211: 113091. PMID 33338869 DOI: 10.1016/j.ejmech.2020.113091  0.13
2023 Li C, He Z, Yao F, Liao S, Sun K, Sun S, Li Z, Wang Z. Role of Escin in breast cancer therapy: potential mechanism for inducing ferroptosis and synergistic antitumor activity with cisplatin. Apoptosis : An International Journal On Programmed Cell Death. PMID 37149513 DOI: 10.1007/s10495-023-01849-x  0.129
2022 Ba S, Luo B, Li Z, He J, Lan F, Wu Y. Mesoporous covalent organic framework microspheres with dual-phase separation strategy for high-purity glycopeptide enrichment. Journal of Chromatography. A. 1684: 463575. PMID 36274529 DOI: 10.1016/j.chroma.2022.463575  0.129
2011 Li C, Lu N, Qi Q, Li F, Ling Y, Chen Y, Qin Y, Li Z, Zhang H, You Q, Guo Q. Gambogic acid inhibits tumor cell adhesion by suppressing integrin β1 and membrane lipid rafts-associated integrin signaling pathway. Biochemical Pharmacology. 82: 1873-83. PMID 21946083 DOI: 10.1016/j.bcp.2011.09.013  0.128
2016 Yang L, Yuan Y, Fu C, Xu X, Zhou J, Wang S, Kong L, Li Z, Guo Q, Wei L. LZ-106, a novel analogue of enoxacin, inducing apoptosis via activation of ROS-dependent DNA damage response in NSCLCs. Free Radical Biology & Medicine. PMID 27012423 DOI: 10.1016/j.freeradbiomed.2016.03.007  0.128
2018 Xu X, Meng Y, Li L, Xu P, Wang J, Li Z, Bian J. Overview of the development of Glutaminase Inhibitors: Achievements and Future Directions. Journal of Medicinal Chemistry. PMID 30148361 DOI: 10.1021/acs.jmedchem.8b00961  0.128
2014 Tao L, Fu R, Wang X, Yao J, Zhou Y, Dai Q, Li Z, Lu N, Wang W. LL-202, a newly synthesized flavonoid, inhibits tumor growth via inducing G(2)/M phase arrest and cell apoptosis in MCF-7 human breast cancer cells in vitro and in vivo. Toxicology Letters. 228: 1-12. PMID 24752227 DOI: 10.1016/j.toxlet.2014.04.002  0.128
2010 Chen FH, Zhang LB, Qiang L, Yang Z, Wu T, Zou MJ, Tao L, You QD, Li ZY, Yang Y, Guo QL. Reactive oxygen species-mitochondria pathway involved in LYG-202-induced apoptosis in human hepatocellular carcinoma HepG(2) cells. Cancer Letters. 296: 96-105. PMID 20580989 DOI: 10.1016/j.canlet.2010.04.004  0.127
2021 Luo B, Li G, Li Z, He J, Zhou J, Wu L, Lan F, Wu Y. Construction of a magnetic covalent organic framework with synergistic affinity strategy for enhanced glycopeptide enrichment. Journal of Materials Chemistry. B. PMID 34296732 DOI: 10.1039/d1tb01168e  0.126
2016 Wang M, Tian W, Wang C, Lu S, Yang C, Wang J, Song Y, Zhou Y, Zhu J, Li Z, Zheng C. Design, synthesis, and activity evaluation of selective inhibitors of anti-apoptotic Bcl-2 proteins: The effects on the selectivity of the P1 pockets in the active sites. Bioorganic & Medicinal Chemistry Letters. PMID 27712939 DOI: 10.1016/j.bmcl.2016.09.061  0.126
2021 Ding H, Pei Y, Li Y, Xu W, Mei L, Hou Z, Guang Y, Cao L, Li P, Cao H, Bian J, Chen K, Luo C, Zhou B, Zhang T, ... Li Z, et al. Design, synthesis and biological evaluation of a novel spiro oxazolidinedione as potent p300/CBP HAT inhibitor for the treatment of ovarian cancer. Bioorganic & Medicinal Chemistry. 52: 116512. PMID 34801827 DOI: 10.1016/j.bmc.2021.116512  0.126
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2012 Zhu B, Zhao L, Zhu L, Wang H, Sha Y, Yao J, Li Z, You Q, Guo Q. Oroxylin A reverses CAM-DR of HepG2 cells by suppressing Integrinβ1 and its related pathway. Toxicology and Applied Pharmacology. 259: 387-94. PMID 22310179 DOI: 10.1016/j.taap.2012.01.019  0.118
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2013 He L, Lu N, Dai Q, Zhao Y, Zhao L, Wang H, Li Z, You Q, Guo Q. Wogonin induced G1 cell cycle arrest by regulating Wnt/β-catenin signaling pathway and inactivating CDK8 in human colorectal cancer carcinoma cells. Toxicology. 312: 36-47. PMID 23907061 DOI: 10.1016/j.tox.2013.07.013  0.115
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